UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
_________________________________________________________________
FORM 10-K
_________________________________________________________________
(Mark One)
☒ ANNUAL REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the fiscal year ended December 31, 2022
or
☐ TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934
For the transition period from ___________ to ___________
Commission File Number: 001-38721
_________________________________________________________________
Axonics, Inc.
(Exact name of registrant as specified in its charter)
_________________________________________________________________
Delaware
(State or other jurisdiction of
incorporation or organization)
26 Technology Drive
Irvine, California
(Address of principal executive
offices)
45-4744083
(I.R.S. Employer
Identification Number)
92618
(Zip Code)
(949) 396-6322
(Registrant’s telephone number,
including area code)
Title of class
Common stock, par value $0.0001 per share
Trading symbol
AXNX
Name of exchange on which registered
Nasdaq Global Select Market
Indicate by check mark if the registrant is a well-known seasoned issuer, as defined in Rule 405 of the Securities Act. Yes ☒ No ☐
Indicate by check mark if the registrant is not required to file reports pursuant to Section 13 or Section 15(d) of the Act. Yes ☐ No ☒
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the Securities Exchange Act of 1934 during the preceding
12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past
90 days. Yes ☒ No ☐
Indicate by check mark whether the registrant has submitted electronically every Interactive Data File required to be submitted pursuant to Rule 405 of Regulation S-T
(§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit such files). Yes ☒ No ☐
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, a smaller reporting company, or an emerging growth
company. See the definitions of “large accelerated filer,” “accelerated filer,” “smaller reporting company,” and “emerging growth company” in Rule 12b-2 of the Exchange
Act.
Large accelerated filer
Non-accelerated filer
☒
☐
Accelerated filer
Smaller reporting company
Emerging growth company
☐
☐
☐
If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised
financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Indicate by check mark whether the registrant has filed a report on and attestation to its management’s assessment of the effectiveness of its internal control over financial
reporting under Section 404(b) of the Sarbanes-Oxley Act (15 U.S.C. 7262(b)) by the registered public accounting firm that prepared or issued its audit report. ☒
If securities are registered pursuant to Section 12(b) of the Act, indicate by check mark whether the financial statements of the registrant included in the filing reflect the
correction of an error to previously issued financial statements. ☐
Indicate by check mark whether any of those error corrections are restatements that required a recovery analysis of incentive-based compensation received by any of the
registrant’s executive officers during the relevant recovery period pursuant to §240.10D-1(b). ☐
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act). Yes ☐ No ☒
The aggregate market value of the registrant’s common stock held by non-affiliates of the registrant as of the last business day of the registrant’s most recently completed
second fiscal quarter was approximately $2,646.8 million, based on the closing price of the registrant’s common stock on the Nasdaq Global Select Market of $56.67 per
share for such date.
As of February 27, 2023, 49,963,601 shares of the registrant’s common stock, par value $0.0001 per share, were outstanding.
DOCUMENTS INCORPORATED BY REFERENCE
The information that is required to be included in Part III of this Annual Report on Form 10-K is incorporated by reference to either a definitive proxy statement or an
amendment to this Annual Report on Form 10-K to be filed by the registrant within 120 days of December 31, 2022. Only those portions of any such definitive proxy
statement that are specifically incorporated by reference herein shall constitute a part of this Annual Report on Form 10-K.
TABLE OF CONTENTS
Special Note Regarding Forward-Looking Statements
Business.
Risk Factors.
Unresolved Staff Comments.
Properties.
Legal Proceedings.
Mine Safety Disclosures.
PART I
PART II
Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity Securities.
[Reserved]
Management’s Discussion and Analysis of Financial Condition and Results of Operations.
Quantitative and Qualitative Disclosures About Market Risk.
Financial Statements and Supplementary Data.
Changes in and Disagreements with Accountants on Accounting and Financial Disclosure.
Controls and Procedures.
Other Information.
Disclosure Regarding Foreign Jurisdictions that Prevent Inspections.
PART III
Directors, Executive Officers and Corporate Governance.
Executive Compensation.
Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters.
Certain Relationships and Related Transactions, and Director Independence.
Principal Accounting Fees and Services.
Exhibits and Financial Statement Schedules.
Form 10-K Summary.
Signatures
PART IV
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Item 1.
Item 1A.
Item 1B.
Item 2.
Item 3.
Item 4.
Item 5.
Item 6.
Item 7.
Item 7A.
Item 8.
Item 9.
Item 9A.
Item 9B.
Item 9C.
Item 10.
Item 11.
Item 12.
Item 13.
Item 14.
Item 15.
Item 16.
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Special Note Regarding Forward-Looking Statements
This Annual Report on Form 10-K contains forward-looking statements within the meaning of Section 27A of the Securities Act of 1933, as
amended (the Securities Act), and Section 21E of the Securities Exchange Act of 1934, as amended (the Exchange Act), that involve risks and
uncertainties, including statements based on our current expectations, assumptions, estimates and projections about future events, our business, financial
condition, results of operations and prospects, our industry and the regulatory environment in which we operate. Any statements contained herein that are
not statements of historical facts may be deemed to be forward-looking statements. In some cases, you can identify forward-looking statements by terms
such as “anticipate,” “believe,” “could,” “estimate,” “expect,” “intend,” “may,” “plan,” “potential,” “predict,” “project,” “should,” “will,” “would” or the
negative of those terms, or other comparable terms intended to identify statements about the future. Forward-looking statements include, but are not limited
to, statements about:
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unanticipated safety concerns related to the use of our products;
• U.S. Food and Drug Administration (FDA) or other U.S. or foreign regulatory or legal actions or changes affecting us or our industry;
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the results of any ongoing or future legal proceedings, including but not limited to intellectual property, product liability or other litigation
against us, our third-party manufacturers or other parties on which we rely or litigation against our general industry;
any termination or loss of intellectual property rights;
any voluntary or regulatory mandated product recalls;
adverse developments concerning our manufacturers or suppliers or any future strategic partnerships;
reduction or interruption in our supply chain and other possible inventory constraints or challenges;
introductions and announcements of new technologies by us, any commercialization partners or our competitors, and the timing of these
introductions and announcements;
successful integration of acquired operations into our ongoing business;
announcements of regulatory approval or disapproval of our products and any future enhancements to our products;
adverse results from or delays in clinical studies of our products;
variations in our financial results or those of companies that are perceived to be similar to us;
success or failure of competitive products or therapies in the markets in which we do business;
changes in the structure of healthcare payments for our products;
announcements by us or our competitors of significant acquisitions, licenses, strategic partnerships, joint ventures or capital commitments;
changes in macroeconomic and market conditions and volatility, including impacts related to the COVID-19 pandemic, risk of recession,
inflation, supply chain constraints or disruptions and rising interest rates;
economic and market conditions in general and in the medical technology industry specifically, including the size and growth, if any, of our
markets, and the issuance of securities analysts’ reports or recommendations;
rumors and market speculation involving us or other companies in our industry;
sales of substantial amounts of our stock by directors, officers or significant stockholders, or the expectation that such sales might occur;
additions or departures of key personnel;
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changes in our capital structure, such as future issuances of securities and the incurrence of additional debt; and
the continued impact of the COVID-19 pandemic, and the related responses of the government and consumers on our business, financial
condition and results of operations.
The forward-looking statements included herein are based on current expectations of our management based on available information and involve
a number of risks and uncertainties, all of which are difficult or impossible to predict accurately and many of which are beyond our control. As such, our
actual results may differ significantly from those expressed in any forward-looking statements. Factors that may cause or contribute to such differences
include, but are not limited to, those discussed in more detail in Item 1 “Business” and Item 1A “Risk Factors” of Part I and Item 7 “Management’s
Discussion and Analysis of Financial Condition and Results of Operations” of Part II of this Annual Report on Form 10-K. Readers should carefully review
these risks, as well as the additional risks described in other documents we file from time to time with the Securities and Exchange Commission (SEC). In
light of the significant risks and uncertainties inherent in the forward-looking statements included herein, the inclusion of such information should not be
regarded as a representation by us or any other person that such results will be achieved, and readers are cautioned not to place undue reliance on such
forward-looking statements. Except as required by law, we undertake no obligation to revise the forward-looking statements contained herein to reflect
events or circumstances after the date hereof or to reflect the occurrence of unanticipated events. You should read this Annual Report on Form 10-K and the
documents we file with the SEC, with the understanding that our actual future results, levels of activity, performance and achievements may be materially
different from what we expect. We qualify all of our forward-looking statements by these cautionary statements.
Unless the context indicates otherwise, as used in this Annual Report on Form 10-K, the terms “Axonics,” “our company,” “we,” “us” and “our”
refer to Axonics, Inc. and our consolidated subsidiaries.
This Annual Report on Form 10-K includes our trademarks and trade names, including, without limitation, Axonics R20™, Axonics F15™ and
Bulkamid®, which are our property and are protected under applicable intellectual property laws. This Annual Report on Form 10-K also includes
trademarks and trade names that are the property of other organizations. Solely for convenience, trademarks and trade names referred to in this Annual
Report on Form 10-K appear without the ® and ™ symbols, but those references are not intended to indicate that we will not assert, to the fullest extent
under applicable law, our rights, or that the applicable owner will not assert its rights, to these trademarks and trade names. We do not intend our use or
display of other companies’ trade names or trademarks to imply a relationship with, or endorsement or sponsorship of us by, any other companies.
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Risk Factors Summary
PART I
The following is a summary of some of the risks and uncertainties as of the date of the filing of this Annual Report on Form 10-K that could materially
adversely affect our business, financial condition, and/or results of operations. You should read this summary together with the more detailed description of
each risk factor contained below.
We have incurred significant operating losses since inception, and we expect to incur operating losses in the future, and we may not be able to
If the quality and benefits of our products do not meet the expectations of physicians or patients, then our brand and reputation or our business
The size and future growth in the market for our products has not been established with precision and may be smaller than we estimate, and our
We have a limited history of manufacturing and assembling our products in commercial quantities and may encounter related problems or delays
Our rechargeable sacral neuromodulation (SNM) system was our sole product until we acquired the Bulkamid urethral bulking agent product line
We may seek to grow our business through acquisitions of complementary products or technologies, and the failure to manage acquisitions, or the
We may require additional capital to finance our planned operations, which may not be available to us on acceptable terms or at all.
We compete against other companies, including Medtronic and Boston Scientific, some of which have longer operating histories, more established
Risks Related to Our Business and Strategy
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achieve or sustain profitability.
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on February 25, 2021 and received FDA approval of our recharge-free SNM system in March 2022. Our SNM systems will generate the majority of our
revenue for the foreseeable future.
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We rely on third parties for the manufacture of our products, some of them as a single source. This reliance increases the risk that we will not have
sufficient quantities of our products or be able to purchase them at an acceptable cost, and reduces our control over the manufacturing process, which could
delay, prevent or impair our development or sales efforts.
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that could result in lost revenue.
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products, or greater resources than we do, which may prevent us from achieving increased market penetration and improved operating results.
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could be adversely affected.
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sales growth may be adversely affected.
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failure to integrate them with our existing business, could harm our business, financial condition and operating results.
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necessary to support our current business strategies.
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hindered.
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not be able to maintain adequate product liability insurance.
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could adversely affect our business.
Risks Related to Legal Matters and Government Regulation
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or alleged failure to comply with applicable requirements could harm our business.
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to grow our business.
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result in costly investigations, fines or sanctions by regulatory bodies.
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require us to recall or withdraw our products from the market.
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Unfavorable global economic conditions could adversely affect our business, financial condition, or results.
Our results may be impacted by changes in foreign currency exchange rates.
A pandemic, epidemic or outbreak of an infectious disease in the United States or worldwide, including the outbreak of the COVID-19 virus,
Our success will depend on our ability to retain senior management and other highly qualified personnel.
If we are unable to achieve and maintain adequate levels of coverage or reimbursement for our products, our commercial success may be severely
We may not receive the necessary clearances or approvals for modifications to our products, and failure to do so would adversely affect our ability
Our operations are subject to extensive laws and government regulation and oversight both in the United States and internationally, and our actual
We face the risk of product liability claims that could be expensive, divert management’s attention and harm our reputation and business. We may
Consolidation in the healthcare industry could lead to demands for price concessions, which may affect our ability to sell our products at prices
Failure to comply with post-market regulatory requirements could subject us to enforcement actions, including substantial penalties, and might
The misuse or off-label use of our products may harm our reputation in the marketplace, result in injuries that lead to product liability suits or
We or any of our suppliers or third-party manufacturers could be forced to recall our products.
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We and our suppliers are subject to various federal, state and foreign laws, including anti-corruption laws, fraud and abuse laws, privacy and
Legislative or regulatory reforms in the United States or Europe may make it more difficult and costly for us to obtain regulatory clearances or
Our products may cause or contribute to adverse medical events or serious safety issues, which could have a negative impact on us.
Litigation or third-party claims of various types could be asserted against us, which could require us to spend significant time and money and
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could affect our business operations and/or stock price.
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approvals, or to manufacture, market or distribute our products.
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security laws, transparency laws, trade regulations, and “conflict minerals” rules, which, if violated, could subject us to substantial penalties. Additionally,
any challenge to or investigation into our practices under these laws could cause adverse publicity and be costly and thus could harm our business.
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Europe, could harm our business, financial condition and results of operations.
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which may be expensive and restrict how we do business.
Our business involves the use of hazardous materials and our third-party manufacturers must comply with environmental laws and regulations,
Healthcare policy changes, including recently enacted legislation reforming the U.S. healthcare system and new medical device regulations in
Risks Related to Intellectual Property
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Litigation or other proceedings or third-party claims of intellectual property infringement against us, including the Medtronic Litigation, or any of
our current or future licensors, including Alfred E. Mann Foundation for Scientific Research (AMF), could require us to spend significant time and money
and could prevent us from selling our products, or affect our stock price.
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If we or any of our current or future licensors, including AMF, are unable to maintain, obtain or adequately protect our intellectual property rights,
we may not be able to compete effectively in our market or we could be required to incur significant expenses to enforce or defend our rights or attempt to
do the same.
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or competitive position could be harmed.
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business.
If we are unable to enforce our intellectual property or protect the confidentiality of our trade secrets or our confidential information, our business
If we fail to comply with our obligations under our patent licenses with third parties, we could lose license rights that are important to our
The trading price of our common stock may be volatile, and purchasers of our common stock could incur substantial losses.
We are obligated to maintain proper and effective internal controls over financial reporting and any failure to do so may adversely affect investor
Risks Related to Our Common Stock
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confidence in us, and, as a result, the value of our common stock.
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actions and proceedings that may be initiated by our stockholders, which could limit our stockholders’ ability to obtain a favorable judicial forum for
disputes with us or our directors, officers, employees or agents.
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trading volume could decline.
Our disclosure controls and procedures may not prevent or detect all errors or acts of fraud.
Anti-takeover provisions in our certificate of incorporation and bylaws, as well as under Delaware law, could discourage a takeover.
Our certificate of incorporation designates the Court of Chancery of the State of Delaware as the sole and exclusive forum for certain types of
If securities or industry analysts do not publish research or publish inaccurate or unfavorable research about our business, our stock price and
Item 1. Business.
Overview
We are a global medical technology company that is developing and commercializing novel products for adults with bladder and bowel
dysfunction, including: (i) implantable SNM systems to treat urinary urge incontinence (UUI) and urinary urgency frequency (UUF), together referred to as
overactive bladder (OAB), as well as fecal incontinence (FI), and non-obstructive urinary retention (UR); and (ii) a urethral bulking agent (Bulkamid) to
treat female stress urinary incontinence (SUI).
SNM Systems
Our newly developed rechargeable SNM system, Axonics R20, is designed to last 20 or more years in the human body and is only 5cc in volume.
R20 provides constant current stimulation and offers broad MRI access with
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1.5T and 3.0T scanners. R20 utilizes an easy-to-use, intuitive patient remote control and requires recharging for only one hour every 6 to 10 months, which
is the longest interval between recharging among rechargeable SNM systems. The R20 replaces the previous rechargeable SNM system offered by Axonics
that was the first to be marketed worldwide.
Our recharge-free SNM system, Axonics F15, utilizes a primary cell battery with an expected life of 15 years at typical stimulation parameters and
over 20 years at lower amplitude settings. The recharge-free implantable neurostimulator (INS) is approximately 10cc in volume, utilizes constant current
stimulation, a recharge-free patient remote control and offers broad MRI access.
We began U.S. commercialization in the middle of the fourth quarter of 2019 after receiving premarket approval (PMA) of our first rechargeable
SNM system by the FDA. We also have marketing approvals from regulators in Europe, Canada, and Australia for all relevant clinical indications.
SNM therapy has been commercially available in the United States for over 20 years and has been clinically proven to provide a safe, effective,
reversible, and long-lasting symptom relief. We believe that our SNM systems offer therapeutic benefits and competitive advantages compared to the
InterStim SNM systems offered by Medtronic. As a result of the longevity of our implantable devices, patients implanted with our SNM systems do not
need to undergo replacement surgery every three to five years, as was the case for patients implanted with legacy non-rechargeable InterStim SNM
systems.
We engineered our SNM systems to deliver constant-current stimulation, which automatically adjusts stimulation based on changes to impedance
that occur as the implanted lead scars into the body, which we believe provides a more consistent therapy over time and reduces management of the
therapy. Our SNM systems include an easy-to-use wireless patient remote control that does not require recharging or replacement batteries. We also
designed and custom built a clinician programmer that guides the implanting physician through lead placement and stimulation programming.
We continue to invest in research and development activities to expand our suite of products for SNM therapy. In March 2022, we received FDA
approval for the Axonics F15, a long-term, recharge-free SNM system. In January 2023, we received FDA approval for the Axonics R20, our fourth-
generation rechargeable SNM system.
We focus most of our sales and marketing efforts in the United States where reimbursement for SNM therapy is well-established and covered by
most major U.S. insurers, including Medicare.
Urethral Bulking Agent
On February 25, 2021, we acquired Contura Limited (Contura) and its Bulkamid product, a urethral bulking hydrogel indicated for the treatment
of female SUI.
SUI is a common condition that afflicts women of all ages, with childbirth as one of the main contributing factors. SUI is caused by weakness in
the pelvic floor, preventing the urethra from closing fully when sudden pressure is put on the bladder. This can allow urine to leak out during normal daily
activities such as coughing, laughing, exercising, or lifting an object.
Bulkamid received a Conformité Européenne (CE) Mark in 2003 and a PMA from the FDA in 2020 and is sold through a combination of a direct
sales force in the United States, Germany, United Kingdom, and the Nordic countries and distributors in certain international markets.
As a next-generation bulking agent, we believe Bulkamid addresses the shortcomings of legacy particulate-based bulking agents. It is a unique and
patented non-particulate hydrogel that is injected into the urethral wall to restore the natural closing pressure of the urethra. It is a simple, quick, and easy-
to-learn and perform procedure that can be performed in either a physician’s office or an outpatient facility.
Bulkamid is biocompatible, consisting of 97.5% water, and does not induce a chronic inflammatory response. Bulkamid’s bulking effect is aided
by the volume of each injection being predictable, controllable, and precise. Bulkamid retains its bulking characteristics for a number of years, thereby
maintaining efficacy and providing women with long lasting relief of their SUI symptoms. Bulkamid is clinically validated and generates high rates of
patient satisfaction.
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Our Strategy
Our goal is to become a global leader in providing effective and long-term solutions to treat incontinence. To achieve this goal, we are pursuing
the following strategies:
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Continue to promote awareness of our SNM systems among healthcare providers. We believe that of the approximately 45,000 physicians
addressing OAB and FI in the United States, approximately 2,000 or less than 5% are actively performing SNM procedures. We intend to help
physicians in their direct-to-patient outreach and are pursuing Axonics-sponsored direct-to-consumer marketing initiatives. We believe this will
increase the number of patients seeking treatment and ultimately undergoing SNM procedures.
Continue to develop a commercialization infrastructure with a dedicated direct sales team. We focus the significant majority of our sales and
marketing efforts in the United States since we believe that approximately 90% of the annual global SNM sales are generated in this market. To
achieve our commercialization goals, we plan to continue to provide our sales representatives and clinical specialists with sufficient resources to
achieve success.
Continuously innovate to introduce enhanced SNM product offerings. We continue to invest in research and development activities to expand
our suite of products for SNM therapy. In March 2022, we received FDA approval for the Axonics F15. In January 2023, we received FDA
approval for the Axonics R20, our fourth-generation rechargeable SNM system.
Further penetrate our initial target market by promoting patient and practice awareness. Currently, we estimate that less than three percent of
patients worldwide that could benefit from SNM therapy have been implanted with an SNM device. We believe that there are several factors that
influence this low historical penetration of the potential market. First, even after patients were made aware of SNM therapy by a physician, many
patients elected not to undergo the procedure due to the limitations of the legacy product, such as the need for multiple INS replacement surgeries
and the large device size. Second, we believe there is a large number of adults with OAB and/or FI symptoms that are unaware of SNM therapy.
Third, we believe that more physicians should offer SNM to their patients. We intend to educate physicians that are unfamiliar with the benefits of
SNM therapy and the attractiveness to patients of our SNM systems. We intend to increase physician and patient awareness through engagement,
direct patient outreach, presentation of clinical data at medical conferences and publication of clinical data in peer reviewed journals.
Expand our product offerings with complementary products in our market. We believe our acquisition of Bulkamid is highly synergistic and
positions us to become a global leader in incontinence solutions. We have been able to leverage our existing commercial footprint of sales and
clinical specialists in the United States and Europe who call on urogynecologists and urologists for SNM, the same type of physicians who treat
SUI. We also believe that extending our urology platform to offer solutions for both OAB and SUI will enhance our value proposition and drive
additional SNM sales.
Our Markets
The market for SNM therapy is large and growing. Our SNM target market consists of millions of adults in the United States and Europe with
symptoms of UUI, UUF, FI, and UR who have progressed through the care pathway and are eligible to be treated with SNM therapy.
We believe that the U.S. SNM market is now approximately $800 million, representing approximately 52,000 annual patient implants. We believe
the SNM market will continue to increase for the foreseeable future driven by increased awareness and education of SNM therapy, greater expectations for
quality of life, and improved patient attitudes toward receiving medical attention. In addition, market growth is anticipated to accelerate due to continued
innovation and the introduction of new efficacious and long-lived products for SNM therapy. We believe that this represents a compelling opportunity for
our SNM systems to capture market share and grow the market for SNM therapy.
The market for SUI therapy is highly underpenetrated, with approximately 22 million women in the United States having moderate to severe SUI
or mixed urinary incontinence (MUI) symptoms, which is urinary
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incontinence related to both stress and urgency. The first-line treatment options for SUI begin with lifestyle changes and continence pessaries. SUI lacks
pharmacologic treatments, with patients next advancing to urethral bulking agents, pelvic floor sling surgery or colposuspension. We estimate that less than
half of these women have sought medical treatment, most of whom were offered conservative therapy or opted for no treatment due to a lack of non-
invasive treatment options with high efficacy.
While we anticipate expanding into other geographic regions over time, we are primarily focusing on marketing our products in the United States
and Europe due to the large overall market size.
Overview of Overactive Bladder
OAB causes a sudden urge to urinate that is difficult to stop and often leads to the involuntary leakage of urine. OAB typically presents via a
combination of several symptoms, including abnormally frequent urination that is typically defined as urinating more than eight times per day, involuntary
leakage of urine, or incontinence, and the disruption of sleep to wake up and pass urine, or nocturia. The combination and severity of OAB symptoms
varies from person to person. UUF, when not accompanied by any other symptoms, does not include the involuntary leakage of urine. UUI is characterized
by the sudden need to urinate accompanied by the involuntary loss of urine, regardless of frequency. Non-obstructive urinary retention or UR, which is the
inability to empty the bladder, is not considered OAB.
A study published in 2022 by Patel, Ushma J. et al. found that approximately 19 million women in the United States have moderate to severe UUI
or MUI symptoms. Study authors utilized publicly available data from the 2015-2018 National Health and Nutrition Examination Survey (NHANES). The
NHANES is a major program of the National Center for Health Statistics, a part of the Centers for Disease Control and Prevention (CDC) and is designed
to assess the health status of a nationally representative sample of the civilian, noninstitutionalized U.S. population. The study analyzed data from over
5,000 women that completed mobile examinations and computer-assisted personal interviews with standardized urinary incontinence questions.
We believe this survey is representative of the prevalence of OAB in the United States. Obesity and diabetes are frequent risk factors associated
with OAB, and we believe that the increase in this high-risk population is one of the factors that has driven continued growth in the prevalence of OAB.
While historically many people with symptoms of OAB have gone undiagnosed, we believe this is beginning to change. We believe that improved
access to care, decreased social acceptance of compromised quality of life, and longer life expectancy may all contribute to individuals being more
proactive about acknowledging symptoms of OAB and seeking medical attention. Previously, patients have avoided discussing their symptoms with
medical professionals because of misperceptions such as OAB symptoms being a normal and accepted consequence of aging, and lack of availability of
treatments, misguided fear of the currently available treatments, and general availability of self-management tools, such as incontinence pads. In addition,
we believe programs such as the Patient Quality Reporting System (PQRS), which was introduced by the Center for Medicaid and Medicare Services
(CMS) in 2013, have helped to improve the frequency of dialogue around OAB between physicians and their Medicare patients as it includes incentives
and penalties for primary care physicians based on various quality of care metrics, one of which addresses treating UUI symptoms.
The prevalence of OAB between women and men is generally similar, however, it varies by subtype. Women are more likely to suffer from UUI
than UUF. In contrast, men are much more likely to suffer from UUF than UUI. Incidence by age also varies between men and women, as women often
develop UUI at much younger ages than men. UUI symptoms in women are often associated with childbirth or menopause, while prostate enlargement,
which is frequently associated with aging, is a leading cause of UUF symptoms in men. SNM is not indicated for treatment of UUF caused by prostate
enlargement. These age and gender differences are significant because they may impact who seeks treatment for symptoms of OAB. Individuals with UUI
are more likely to seek treatment due to the impact of incontinence on quality of life, and younger individuals are less likely to dismiss symptoms of OAB
as an expected consequence of aging. As a result, women are more likely to seek treatment for symptoms of OAB than men.
Symptoms consistent with a diagnosis of OAB can develop due to a variety of underlying causes. When a patient consults a physician for the
treatment of their symptoms related to OAB, the physician will first undertake a differential diagnosis in an attempt to determine the underlying cause of
OAB.
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If the physician is able to identify an underlying cause of OAB, the physician will then attempt to treat the underlying cause and alleviate the
symptoms. When the physician is unable to identify an underlying cause of OAB symptoms, the patient is considered to have idiopathic OAB. We believe
that these idiopathic patients are some of the best candidates for SNM therapy and where SNM therapy has been clinically proven to alleviate the
symptoms associated with OAB.
OAB is associated with a significant economic burden to society. Direct medical and non-medical costs associated with OAB include the cost of
diagnostics, pharmacological care, routine care, and OAB-related consequences such as urinary tract infections, skin infections, and depression. Further,
indirect costs of OAB include caregiver wages and worker productivity losses resulting either from disability or absenteeism, as well as intangible costs
including the quality-of-life impact and psychological burden. According to a study published in the American Journal of Managed Care in 2009, these
OAB costs result in a total economic burden in the United States that is estimated to be between $24.9 billion and $36.5 billion.
Before treating patients with a third-line therapy such as SNM, physicians are required to prescribe first- and second-line therapies. As discussed
further below, first-line therapies including behavioral changes such as diet and exercise, and second-line therapies include drug therapy. In the United
States, in order to secure reimbursement, physicians are required to prescribe, and the patient must fail, or be contraindicated and/or refractory for, up to
two second-line drug therapies before beginning SNM therapy, although the course of treatment and its duration may vary patient-by-patient based on
physician judgment.
Current Treatments for OAB and Limitations
Patients with OAB follow a care pathway that transitions them, as necessary, through the progressive series of OAB treatment options. The care
pathway directs physicians as to the progression of OAB treatments as follows:
• First-line therapy: behavioral changes, including conservative treatment options such as diet, exercise, timed voiding, pelvic floor exercises, and
biofeedback;
• Second-line therapy: drug therapy, including two classes of OAB drugs, anti-muscarinics and beta-3 adrenergic agonists, with patients often trying
multiple drugs; and
• Third-line therapy: minimally invasive therapy consisting of SNM, BOTOX injections and non-implantable Percutaneous Tibial Nerve Stimulation
(PTNS).
First- and second-line therapies comprise the largest segment of the treatment market and are better known to physicians and hospitals than SNM
therapy.
First-Line Therapies
First-line therapies represent conservative treatment options. Physicians may recommend that a patient make behavior modifications, such as
drinking less fluid, training the bladder and/or pelvic muscles through Kegel exercises, among others. Such treatment options are limited in both duration
and effectiveness.
Second-Line Therapies
Second-line therapies consist of medications, which comprise the largest segment of the OAB treatment market. Anticholinergics such as
Oxybutynin, Vesicare, Detrol, Oxytrol, Enablex, and Sanctura are the most commonly prescribed medications. However, patients often do not fully comply
with their drug prescriptions, due to perceived inefficacy and side effects. Mirabegron and Vibegron are the only available beta-3-adrenergic agonists that
targets the bladder muscles and reduces bladder contractions to treat OAB. Physicians may also prescribe Tricyclic antidepressants such as Duloxetine and
Imipramine, which are not FDA approved to treat the symptoms of OAB, but have been shown to relax the muscles in the bladder and reduce urgency.
Anti-muscarinic drugs inhibit the activation of muscarinic receptors on the bladder muscle by acetylcholine. Dry mouth is the most bothersome
adverse event associated with antimuscarinic drugs and often a reason for treatment discontinuation. Side effects also include blurred vision, photophobia,
tachycardia, difficulty in urination, hyperthermia, glaucoma, and mental confusion in the elderly.
Beta3-adrenergic agonists are relatively new drugs for OAB that work by relaxing the bladder muscle in the wall of the bladder by stimulating the
beta-3 receptors that are found on the surface of the muscle cells. This
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relaxation of the bladder muscle helps to increase the capacity of the bladder to hold urine. In turn, this reduces the need to pass urine. The most common
adverse events observed in clinical trials were hypertension, nasopharyngitis, and urinary tract infection.
Third-Line Therapies
Sacral Neuromodulation
Medtronic’s InterStim I was approved by the FDA to treat the symptoms of UUI in 1997 and UUF in 1999. InterStim II was approved to treat the
symptoms of OAB by the FDA in 2005, and to treat the symptoms of FI in 2011. Medtronic’s InterStim Micro was approved by the FDA in 2020 and
InterStim X was approved by the FDA in 2022. These systems have been implanted in hundreds of thousands of patients, with a majority of all implants
having taken place in the United States.
BOTOX Injections
BOTOX injections into the bladder muscle were approved for treatment of symptoms of OAB by the FDA in 2013. BOTOX is injected through a
cystoscopic procedure in a clinician’s office or the outpatient surgery setting, and BOTOX treats OAB by blocking the signal from the bladder nerves to the
bladder muscle. Key adverse events include recurrent urinary tract infections and self-catheterization due to inability to void. BOTOX injections are
typically required every six to 12 months to maintain reduction of OAB symptoms. We believe the frequent need for injections and the adverse event
profile are deterrents to initial and long-term preference for BOTOX injections, as evidenced by an approximately 60% rate of cessation of BOTOX
injections at three years, according to a retrospective study by Mohee et al. 2012.
Percutaneous Tibial Nerve Stimulation
PTNS involves in-office placement of an acupuncture needle in a patient’s ankle to deliver electrical stimulation to the tibial nerve. Typically,
patients undergo a 12-week trial period of weekly 60-minute PTNS sessions to evaluate whether the therapy provides significant symptom reduction. After
this period, patients that continue with the therapy typically require monthly treatments to maintain symptom reduction. Adverse events of PTNS are
minimal; however, lack of PTNS efficacy and lack of patient compliance result in PTNS generally providing less long-term effectiveness than SNM and
BOTOX injection therapies.
Overview of Fecal Incontinence
FI is the inability to control bowel function, causing involuntary or accidental leakage from the rectum. Stimulation of the sacral nerves can reduce
incontinence episodes, urgency, and frequency in people suffering from FI, and is an approved therapy for the treatment of FI in the United States and
Europe. Moreover, a significant population of people suffering from FI also exhibit symptoms of OAB. SNM therapy can alleviate symptoms in patients
suffering from either or both OAB and FI. Adults with FI that exhibit idiopathic symptoms or experience FI as result of obstetric or surgical injury or other
prior trauma can be treated with SNM therapy.
People with FI experience even greater degrees of embarrassment and decreased quality of life than people with OAB. We believe shifting
expectations and attitudes toward medical attention suggest this addressable market has the potential to expand.
A study published in 2014 by Ditah, Ivo et al. found that approximately 19 million adults in the United States exhibited symptoms of FI. Study
authors utilized publicly available data from the 2005-2010 NHANES sample and based their analysis on over 14,000 adults that completed the FI section
of the survey.
Symptoms consistent with a diagnosis of FI can develop due to a variety of underlying causes. When a patient consults a physician for the
treatment of their symptoms related to FI, the physician will first undertake a differential diagnosis in an attempt to determine the underlying cause of FI.
Underlying issues that can cause FI include obstetric injury, inflammatory diseases, prior surgeries, and other issues.
If the physician is able to determine that FI is caused by a clear, underlying disease, such as inflammatory bowel disease, the physician will then
prescribe a care pathway to treat the underlying disease and alleviate the symptoms. Patients with FI caused by past trauma, mainly from obstetric damage,
represent the majority of
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candidates for treatment of FI with SNM therapy. Additionally, in the absence of an identified underlying cause of FI symptoms, the patient is considered to
have idiopathic FI.
Our SNM Systems
We believe that our proprietary SNM systems provide a minimally invasive, effective, and long-lasting solution for patients with bladder and
bowel dysfunction. We have marketing approvals in the United States, Europe, Canada, and Australia for all relevant clinical indications.
Our SNM systems include two implantable components and various external components.
Implantable Components for Patient
• Miniaturized INS, which houses the electronics for the device. The Axonics R20 is the fourth-generation rechargeable SNM system that utilizes an
INS that is 5cc in volume and is intended to provide six to ten months of battery life between charges under normal use conditions. The Axonics
F15 is a recharge-free SNM system that utilizes an INS that is 10cc in volume and powered by a primary cell battery.
•
Tined four-electrode lead, which is implanted next to the targeted sacral nerve and delivers stimulation to the nerve. The tines help anchor the lead
in its desired position.
Implantable Neurostimulators
External Components for Patient
F15 and R20
• Wireless charging device, which allows transcutaneous charging of the Axonics R20 INS. The charger uses an easy-to-understand combination of
visual, audio and haptic indicators to provide information about the charging status. Further, it has the ability to be held into position by an
adhesive fixation device or a reusable and flexible belt, which significantly enhances patient mobility.
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• Wireless remote control that communicates with the device at a range of up to approximately three feet, which is a small and easy-to-use device
that allows the patient to adjust stimulation intensity levels, modify program settings and turn stimulation on or off. The remote control includes a
light-emitting diode light that indicates therapy intensity and the status of battery life of the INS.
Wireless Charging Device
The implantable components of our SNM systems deliver mild electrical pulses to the targeted sacral nerve, most frequently the S3 nerve, in order
to correct the dysfunction by restoring normal communication to and from the brain. The sacral nerves, including the S3 nerve, are located in the pelvic
area and are responsible for controlling urethral sphincters, the bladder and anal sphincter muscles. The image below illustrates the location of the two
implantable components of our INS and the four-electrode lead:
Patient Remote Control
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Benefits of our SNM Systems
We believe that our innovative and proprietary SNM systems offer several competitive advantages as compared to the legacy SNM system,
InterStim II. Our SNM systems offer the following important benefits:
•
Long-term solution. Our devices are designed to last 15 to 20 or more years, compared to 7-10 years for the InterStim X.
• Material benefits to physicians and payors. We believe our SNM systems have the potential to enable physicians and facilities to utilize their
resources more efficiently and significantly reduce overall costs to the healthcare system, due to the need for less replacement surgeries compared
to InterStim.
•
Small and lightweight implantable neurostimulator. Our rechargeable INS is approximately 60% smaller than InterStim X and our recharge-
free INS is approximately 30% smaller than InterStim X.
• Constant current. Our SNM systems deliver constant-current stimulation, which automatically adjusts stimulation based on changes to
impedance that occur as the implanted lead scars into the body and we believe provides a more consistent and reliable therapy.
In addition, we believe our SNM systems offer many additional competitive advantages compared to the InterStim product line:
Improved patient experience. Our SNM systems include a discrete, small and easy-to-use remote control.
Simplified therapy programming. Our clinician programmer guides the provider through electrode stimulation programming and enables
providers to access key data from the patient’s INS.
Broad MRI conditions. Our SNM systems allow for 1.5T and 3T full-body MRI scans under broad conditions.
•
•
•
• Clinically proven results. Our rechargeable SNM system with clinical data to support its safety and efficacy. Two-year results from our clinical
study show that 93% of patients achieved clinically significant improvements.
Overview of our External Trial System
Our external trial system (ETS) can be used during an evaluation period by a physician to determine if a patient is a good candidate for SNM
therapy. This system includes a disposable external stimulation device, a disposable implantable lead, and a patient remote control. The external stimulation
device is comprised of a temporary, non-rechargeable, current controlled pulse generator. The temporary implantable lead has a single electrode. In
addition, our ETS can be used for a bilateral percutaneous nerve evaluation trial or a tined lead evaluation trial.
Overview of our Physician Tools
We provide physicians with a surgical tool kit to assist them while implanting our SNM systems. Our clinician programmer also allows physicians
to connect to a patient’s INS during the implant procedure and at other times to access key therapy data that is stored and maintained on the INS.
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Clinician Programmer
We designed and custom built our touchscreen clinician programmer. The INS is programmed by and wirelessly communicates with the clinician
programmer. This programmer is designed to simplify and assist physicians with electrode placement and stimulation programming. It has a series of
touchscreens with a graphical user interface that provides information to the physician, such as measured data, test stimulation adjustments, and electrode
configurations based on the utilization of proprietary algorithms. Further, it enables the clinician programmer to access any INS data and its complete
history. The clinician programmer records and stores all data from the INS and enables a physician to store and retrieve this data electronically.
Surgical Tool Kit
The single-use surgical tool kit provides the physician with the tools necessary for the SNM implant procedure.
Clinician Programmer
Treatment with our SNM Systems
Patient Selection
SNM therapy is an approved therapy for patients with symptoms of bladder and bowel dysfunction. This therapy is not intended for patients with a
mechanical obstruction such as benign prostatic hyperplasia, a tumor, or urethral stricture. Further, the therapy is not indicated for pregnant women or
pediatric use.
SNM therapy for bowel dysfunction is indicated for patients who are not candidates for more conservative treatments. The therapy is not indicated
for pregnant women or pediatric use.
Implantation
Before receiving an Axonics SNM system, a patient in the United States typically undergoes an external trial period.
External Trial Period
The short external trial procedure, which typically lasts approximately 30 minutes, is generally performed in the office or outpatient setting and
typically involves a percutaneously placed lead, which a physician implants near the targeted sacral nerve using a needle, with the location confirmed
utilizing fluoroscopy and intraoperative muscle responses evoked by test stimulation. The lead is then connected to a temporary, disposable external trial
stimulator, which provides stimulation for the therapy. The trial period can last between a few days to several weeks after which the physician evaluates the
effectiveness of SNM therapy through several measures, including bladder or bowel episodes and patient satisfaction. The vast majority of patients proceed
from an external trial to permanent
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implant; the percentage of conversion is dependent on the quality of the implant procedure, external trial type and patient response to the stimulation.
Permanent Implant
Patients who have undergone a successful external trial period are eligible for a permanent INS implant procedure. The permanent implant
procedure typically occurs in an ambulatory surgical center or hospital outpatient setting, usually lasting under an hour, and includes implantation of the
INS and, if a temporary lead was used for the trial, implantation of the permanent lead. The INS is inserted through a small incision into a pocket in the
subcutaneous fat of the upper buttocks, and the lead body is tunneled to the INS pocket and connected to the INS.
Activation and Programming
Immediately following the implant procedure or within a week thereafter, the patient has their stimulation settings programmed. Stimulation
settings are adjusted to ensure they are comfortable to the patient. A reprogramming session may be necessary to achieve and maintain symptom reduction
or to address discomfort. After initial programming, a patient has the ability to modify the therapy with the patient remote control.
Our Clinical Results and Studies with our SNM Systems
We have a body of compelling clinical evidence that demonstrates the safety, effectiveness, and sustained benefits of our SNM systems. We have
two clinical studies relating to our rechargeable SNM system, a European study, RELAX-OAB, and a U.S. pivotal study, ARTISAN-SNM.
In June 2018, we completed the enrollment and implantation of 129 patients with UUI for our ARTISAN-SNM pivotal study. These patients were
evaluated at 14 centers in the United States and five centers in Europe. All patients in our ARTISAN-SNM study reached the two-year post-implant follow-
up by August 2020, resulting in completion of the ARTISAN-SNM study.
Key highlights of our ARTISAN-SNM pivotal study at two-years are as follows:
•
•
•
113 of the 121 implanted patients completing the two-year visit, or 93%, were therapy responders. Of the 129 patients initially treated, 88%
were therapy responders at two years (113 out of 129);
93 of the 113 therapy responses, or 82%, had a ≥75% reduction in urgency incontinence episodes;
94% of patients reported being “satisfied” with the therapy; and
• No serious device-related adverse events have been reported.
Our European RELAX-OAB study began in June 2016 and evaluated 51 patients at seven sites in Europe with OAB subtypes UUI and/or UUF.
All patients were evaluated to determine if they were therapy responders, which was defined as showing at least a 50% reduction in the number of average
leaks or voids per day or a reduction to less than eight voids per day, in each case on a three-day bladder diary, at various times post-implant. We are
following patients out to two years in this study and may follow patients out to five years at selected study sites.
Key highlights of our European RELAX-OAB study at two-years are as follows:
•
•
Therapy responder rate for the 37 patients who continued with study follow-up was 90% for test responders and 76% for all implanted
patients;
93% of test responders and 87% of all implanted patients were “satisfied” with the therapy provided by our rechargeable SNM system; and
• No serious device-related adverse events have been reported.
Our Bulkamid Product
Bulkamid is a urethral bulking agent in the form of a non-particulate hydrogel, consisting of 97.5% water and 2.5% polyacrylamide. Bulkamid is
injected into the soft tissue of the urethra, adding volume to narrow the lumen of the urethra and to support the closing mechanism of the urethra, thus
preventing urine leakage. Urethral bulking does not close the urethra totally; the urethra still opens normally to allow for urination.
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Bulkamid achieves its bulking effect by the volume of the gel injected, unlike competitive bulking agents that achieve bulking effect through their
micro particles and the body’s inflammatory reaction to the particles.
Over 150,000 women with SUI have been treated with Bulkamid across 25 countries since receiving regulatory approval. During that time, there
have been no reported long-term complications or adverse events.
The Bulkamid procedure is minimally invasive, with no cuts or incisions necessary, and typically takes less than 15 minutes. It is a simple
procedure that is easy for physicians to learn and is usually performed in a physician’s office or an outpatient facility, typically utilizing a local anesthetic.
The injections are made into 3 to 4 locations in the urethral wall; the total volume injected is approximately 2 mL, equivalent to half a teaspoon. The patient
is able to return home shortly following the procedure.
The majority of women treated with Bulkamid report dryness or improvement in their symptoms, with many seeing that improvement as soon as
they leave the physician’s office, hospital or clinic. Whilst experiencing no leakage at all is the most desired outcome of treatment, many women consider a
successful treatment to be a meaningful decrease in the amount and frequency of urine leakage due to SUI such that they can go about their daily activities.
If relief from symptoms is not sufficient, an additional injection of Bulkamid (a “top-up” injection) can be given to help achieve desired results.
In Bulkamid clinical studies, women were asked how effective their treatment was 12 months after their initial injection. Over three quarters of
women reported that their incontinence was either cured or improved in one study, while in another study approximately two-thirds of women reported
being dry. A Bulkamid clinical study has also shown that most of the women treated over 7 years ago still report a benefit.
Sales and Marketing
We are primarily focused on commercializing our products in the United States, which accounts for the vast majority of sales worldwide. We have
established a significant commercial infrastructure, with approximately 140 sales representatives and approximately 185 clinical and therapy support
specialists in the United States. We continue to make significant investments to build our commercial organization to market and support our products.
When making hiring decisions for these roles, we prioritize individuals with strong sales backgrounds who also have existing relationships with urologists
and urogynecologists. We expect to focus the significant majority of our sales and marketing efforts in the United States where reimbursement for our
therapies are well established and covered by most major U.S. insurers, including Medicare.
Through our specialized and dedicated direct sales organization, we are targeting urologists, urogynecologists and colorectal surgeons, primarily
those who have experience performing SNM procedures.
In order to support our direct sales team, our clinical staff is primarily responsible for attending SNM implant procedures and assisting the
implanting physician with programming the device. Based on our experience to date, we believe that physicians require minimal training to start implanting
our SNM systems.
We are promoting broader awareness of SNM and Bulkamid therapies for the treatment of OAB among patients and physicians, as well as
awareness of the benefits and advantages of our products. We have expanded our awareness raising activities, including direct to consumer advertising on
Facebook and national television ads, publication of scientific data in peer reviewed journals and education of physicians.
Although our main commercial priority is the United States, in November 2018, we launched a limited commercial effort in Europe. With the
addition of the Bulkamid international sales force, we currently have approximately 21 dedicated sales representatives and clinical specialists in the United
Kingdom, Germany, Netherlands, the Nordic countries, Canada, and Australia, with distributors serving certain other international markets around the
world.
Third-Party Coverage and Reimbursement
In the United States, we derive revenue from the sale of our products to hospitals and ambulatory surgical centers, which typically bill various
third-party payors, including Medicare, Medicaid, private insurance companies, health maintenance organizations and other healthcare-related
organizations. In addition, we expect that any portion of the costs and fees associated with our SNM systems that are not covered by these third-party
payors, such as deductibles or co-payments, will be billed directly to the patient by the provider. Third-party payors require
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physicians and hospitals to identify the product and service for which they are seeking reimbursement by using Current Procedural Terminology (CPT)
codes, which are created and maintained by the American Medical Association. As SNM therapy has been widely used in patients for over 20 years in the
United States, reimbursement codes and payments are well-established and the procedure is covered by Medicare, Medicaid and private health insurance
plans. Similarly, urethral bulking agent treatment reimbursement codes and payments are well-established and the procedure is covered by Medicare,
Medicaid and private health insurance plans.
Physician reimbursement under Medicare is generally based on a defined fee schedule (the Physician Fee Schedule), through which payment
amounts are determined by the relative value of the service rendered by the physician. Medicare generally provides reimbursement to hospitals and
ambulatory surgical centers for SNM therapy under the hospital outpatient prospective payment system and the Ambulatory Surgical Center Payment
System, respectively, which reimburse to the hospital or ambulatory surgical center, as applicable, a bundled amount generally intended to cover all facility
costs related to procedures performed in the outpatient setting. The typical Medicare payment for facility and physician services for an SNM trial and full
system implant ranges from approximately $23,000 to approximately $27,000, which covers the cost for the devices and the implantation procedures.
SNM procedures are eligible for payment under existing CPT code 64561 for percutaneous implantation of a lead near the sacral nerve and CPT
code 64590 for insertion or replacement of a peripheral or gastric neurostimulator, which includes a neurostimulator for SNM therapy. Reimbursement
rates vary based on several factors, including but not limited to the payor, geographic location, the procedure performed, contract terms, the facility in
which the procedure is performed and other factors.
Most large insurers have established coverage policies in place to cover SNM therapy. Certain commercial payors have a patient-by-patient prior
authorization process that must be followed before they will provide reimbursement for SNM therapy. These processes typically involve the treating
physician submitting a form to the payor that provides information about the past treatments provided to the patient that proved ineffective, and the
physician’s recommendation that the patient be treated with SNM therapy. Although the prior authorization process can take several weeks, based on our
industry knowledge, it generally results in positive coverage determination for these patients.
Outside the United States, reimbursement levels vary significantly by country and by region, particularly based on whether the country or region
at issue maintains a single-payor system. SNM therapy is eligible for reimbursement in Canada, Australia and certain countries in Europe. Annual
healthcare budgets generally determine the number of SNM systems that will be paid for by the payor in these single-payor system countries and regions.
Reimbursement is obtained from a variety of sources, including government-sponsored and private health insurance plans, and combinations of both. Some
countries or regions may require us to gather additional clinical data before granting coverage and reimbursement for our SNM systems.
Research and Development
We continue to invest in research and development activities to expand our suite of products for SNM therapy. Research and development
expenses were approximately $34.4 million, $37.3 million, and $29.1 million for the years ended December 31, 2022, 2021, and 2020, respectively.
Manufacturing and Supply
We use a combination of in-house and outsourced vendors to manufacture various components of our products. Our contract manufacturers all
have quality systems established that meet FDA requirements and are all recognized in their field for their competency to manufacture the respective
portions of our SNM systems. We believe the manufacturers we currently utilize have sufficient capacity to meet our requirements and are able to scale up
their capacity relatively quickly with limited capital investment. Certain components used in our products are supplied by single-source suppliers. Our
suppliers manufacture the components they produce for us and test our components and devices to our specifications. We intend to maintain sufficient
levels of inventory to enable us to continue our operations while we obtain another supplier in the event that one or more of our single-source suppliers
were to encounter a delay in supply or end supply.
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We employ a rigorous supplier assessment, qualification, and selection process targeted to suppliers that meet the requirements of the FDA and the
International Organization for Standardization (ISO), and quality standards supported by internal policies and procedures. Our quality assurance process
monitors and maintains supplier performance through qualification and periodic supplier reviews and audits. We are required to maintain ISO 13485
certification for medical devices sold in the European Economic Area (EEA), which requires, among other items, an implemented quality system that
applies to component quality, supplier control, product design and manufacturing operations.
We inspect, test, and assemble our products under strict manufacturing processes supported by internal policies and procedures. We perform our
own final quality control testing of each product. However, we do not have complete control over all aspects of the manufacturing process of, and are
dependent on, our contract manufacturing partners for compliance with current Good Manufacturing Practice (cGMP) regulations applicable to
our products.
Our suppliers are managed through our supplier management program that is focused on reducing supply chain risk. Key aspects of this program
include managing component inventory at the supplier, contractual requirements for last time buy opportunities and second sourcing approaches for
specific suppliers. Typically, our outside vendors produce the components to our specifications and in many instances to our designs. Our suppliers are
audited periodically by our quality department to ensure conformity with the specifications, policies and procedures for our devices. In addition, we and our
suppliers are subject to periodic unannounced inspections by U.S. and international regulatory authorities to ensure compliance with quality regulations.
We believe that, if necessary, alternative sources of supply would be available in a relatively short period of time and on commercially reasonable terms.
For our off-the-shelf components, we do not have long-term supply agreements with many of our third-party manufacturers, and we purchase
certain components of our products on a purchase order basis. We may be unable to establish any agreements with third-party manufacturers or to do so on
acceptable terms. We do not currently have arrangements in place for redundant supply of certain components of our products. If our current third-party
manufacturers cannot perform as agreed, we may be required to replace those manufacturers or expand our in-house manufacturing, which could require
significant capital investments. Although we believe that there are several potential alternative manufacturers who could manufacture these components,
we may incur added costs and delays in identifying and qualifying any such replacement. We believe our manufacturing capacity is sufficient to meet
global market demand for our products for the foreseeable future.
As previously discussed, and pursuant to the Manufacturing and Supply Agreement, Contura International manufactures all of the Bulkamid that
we sell. We have rights to a technology transfer after June 30, 2022 that would enable us to insource the manufacturing of Bulkamid. Under the
Manufacturing and Supply Agreement, Contura International is responsible for obtaining and maintaining all necessary permits, licenses, approvals and
authorizations required for the manufacture and sale of Bulkamid. The Manufacturing and Supply Agreement is subject to certain maximum purchase
amounts of Bulkamid, which we believe are sufficient to meet the projected global demand for Bulkamid.
Competition
We believe our products offer several improvements for patients, physicians, and payors.
We consider our primary competition to be implantable SNM devices offered by Medtronic. Medtronic’s InterStim X and InterStim Micro are
currently the only other implantable SNM devices approved for commercial sale in the United States by the FDA. We also compete with other third-line
treatments, such as BOTOX injections, a product sold by Allergan plc, PTNS, as well as more invasive surgical treatment options, and drugs for the
treatment of OAB and FI. We also face competition from Boston Scientific for the treatment of SUI with its bulking agent. In addition, emerging businesses
may be in the early stages of developing additional products or therapies designed to treat OAB, FI or SUI.
Intellectual Property
We rely on a combination of patent, copyright, trademark and trade secret laws, and confidentiality and invention assignment agreements, to
protect our intellectual property rights.
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We own numerous issued patents and pending patent applications that relate to our SNM systems and several issued patents and patent
applications were licensed from AMF in 2013 pursuant to the License Agreement. As of December 31, 2022, we own 48 issued U.S. patents and 143
issued foreign patents, and 31 pending U.S. patent applications and 22 pending foreign patent applications. We also license from AMF 30 issued U.S.
patents and one pending U.S. patent application, as well as 52 issued foreign patents and three pending foreign patent applications. Issued patents owned or
used by us will expire between 2023 and 2043.
In addition, we own or have rights to trademarks and domains in the United States and select locations internationally that we use in connection
with the operation of our business.
We also rely upon trade secrets, know-how and continuing technological innovation, and may in the future rely upon licensing opportunities, to
develop and maintain our competitive position. We protect our proprietary rights through a variety of methods, including confidentiality agreements and
proprietary information agreements with third party contract manufacturers, suppliers, employees, consultants and others who may have access to
proprietary information that we own or license for use.
AMF License Agreement
On October 1, 2013, we entered into the License Agreement, pursuant to which AMF licensed us the AMF IP relating to AMF Licensed Products.
Under the License Agreement, for each calendar year beginning in 2018, we are obligated to pay AMF a royalty on an AMF Licensed Product-by-
AMF Licensed Product basis if one of the following conditions applies: (i) one or more valid claims within any of the patents licensed to us by AMF covers
such AMF Licensed Products or the manufacture of such AMF Licensed Products, or (ii) for a period of 12 years from the first commercial sale anywhere
in the world of such AMF Licensed Product, in each case. The foregoing royalty is calculated as the greater of (a) 4% of all net revenue derived from the
AMF Licensed Products, and (b) a minimum annual royalty (the Minimum Royalty), payable quarterly. The Minimum Royalty automatically increases
each year, subject to a maximum amount of $200,000 per year. During the years ended December 31, 2022, 2021, and 2020, we have recorded royalties of
$3.3 million, $6.3 million, and $4.4 million, respectively.
Government Regulation Applicable to Us
Our products and our operations are subject to extensive regulation by the FDA and other federal and state authorities in the United States,
including the U.S. Department of Justice (DOJ), the Department of Health & Human Services - Office of the Inspector General (HHS-OIG), the United
States Federal Communications Commission (FCC), the CMS, the Federal Trade Commission (FTC), as well as comparable authorities in the EEA,
Australia, and Canada. These government authorities continue to highly scrutinize our industry. Our products are subject to regulation as a medical device
under the Federal Food, Drug, and Cosmetic Act (FDCA), as implemented and enforced by the FDA. The FDA regulates the development, design, non-
clinical and clinical research, manufacturing, safety, efficacy, labeling, packaging, storage, installation, servicing, recordkeeping, premarket clearance or
approval, import, export, adverse event reporting, advertising, promotion, marketing and distribution, and import and export of medical devices to ensure
that medical devices distributed domestically are safe and effective for their intended uses and otherwise meet the requirements of the FDCA.
In addition to U.S. regulations, we are subject to a variety of regulations in the EEA, Australia, and Canada governing clinical studies and the
commercial sales and distribution of our products. We will be required to obtain authorization under appropriate regulatory authorities in countries outside
the United States before commencing clinical studies and to obtain marketing authorization or approval before we can commercialize our product in those
countries, whether or not we have or are required to obtain FDA clearance or approval for a product. The approval process varies from country to country
and the time may be longer or shorter than that required for FDA clearance or approval.
FDA Premarket Clearance and Approval Requirements
Unless an exemption applies, each medical device commercially distributed in the United States requires either FDA clearance of a 510(k)
premarket notification or PMA approval.
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Devices deemed by the FDA to pose the greatest risks, such as life-sustaining, life-supporting or some implantable devices, or devices that have a
new intended use, or use advanced technology that is not substantially equivalent to that of a legally marketed device, are placed in Class III, requiring
approval of a PMA. Devices for which there is no predicate device and which therefore are not eligible for 510(k) review, but project a low-to-
moderate risk may be eligible for the de novo review process.
Our SNM systems are Class III devices and as such, we obtained PMA approval to market our devices for the treatment of OAB, FI and UR.
In a PMA, the manufacturer must demonstrate that the device is safe and effective. The PMA is typically supported by data from preclinical
studies and human clinical studies. The PMA must also contain a full description of the device and its components, a full description of the methods,
facilities and controls used for manufacturing, and proposed labeling. In addition, the FDA will generally conduct a preapproval inspection of the applicant
or its third-party manufacturers’ or suppliers’ manufacturing facility or facilities to ensure compliance with applicable portions of the Quality Systems
Regulation (QSR).
Certain changes to an approved device, such as changes in manufacturing facilities, methods, or quality control procedures, or changes in the
design performance specifications, which may affect the safety or effectiveness of the device, require submission of a PMA supplement. PMA supplements
often require submission of the same type of information as a PMA, except that the supplement is limited to information needed to support any changes
from the device covered by the original PMA and may require no clinical data or less extensive clinical data than the original PMA or the convening of an
advisory panel. Certain other changes to an approved device require the submission of a new supplement or PMA, such as when the design change causes a
different intended use, mode of operation, and technical basis of operation, or when the design change is so significant that a new generation of the device
will be developed, and the data that were submitted with the original PMA are not applicable for the change in demonstrating a reasonable assurance of
safety and effectiveness.
Post-market Regulation - United States
After a device is cleared or approved for marketing, numerous and pervasive regulatory requirements continue to apply. These include:
•
establishment, registration and device listing with the FDA;
• QSR requirements, which require manufacturers, including third-party manufacturers, to follow stringent design, testing, control, documentation
and other quality assurance procedures during all aspects of the design and manufacturing process;
•
•
•
•
labeling and marketing regulations, which require that promotion is truthful, not misleading, fairly balanced and provide adequate directions for
use and that all claims are substantiated, and also prohibit the promotion of products for unapproved or “off-label” uses and impose other
restrictions on labeling;
the federal Physician Payments Sunshine Act and various state and foreign laws on reporting remunerative relationships with health care
providers;
the U.S. Anti-Kickback Statute (and similar state laws) prohibiting, among other things, soliciting, receiving, offering or providing remuneration
intended to induce the purchase or recommendation of an item or service reimbursable under a federal healthcare program, such as Medicare or
Medicaid. A person or entity does not have to have actual knowledge of this statute or specific intent to violate it to have committed a violation;
the U.S. False Claims Act (and similar state laws) prohibiting, among other things, knowingly presenting, or causing to be presented, claims for
payment or approval to the federal government that are false or fraudulent, knowingly making a false statement material to an obligation to pay or
transmit money or property to the federal government or knowingly concealing, or knowingly and improperly avoiding or decreasing, an
obligation to pay or transmit money to the federal government. The government may assert that items or services resulting from a violation of the
federal Anti-Kickback Statute constitutes a false or fraudulent claim for purposes of the False Claims Act;
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•
clearance or approval of product modifications to 510(k)-cleared devices that could significantly affect safety or effectiveness or that would
constitute a major change in intended use of a cleared device, or approval of a supplement for certain modifications to PMA devices;
• medical device reporting regulations, which require that a manufacturer report to the FDA if a device it markets may have caused or contributed to
a death or serious injury, or has malfunctioned and the device or a similar device that it markets would be likely to cause or contribute to a death or
serious injury, if the malfunction were to recur;
•
•
•
correction, removal and recall reporting regulations, under which the FDA can order device recalls under certain circumstances and that require
manufacturers report to the FDA voluntary field corrections and product recalls or removals if undertaken to reduce a risk to health or to remedy a
violation of the FDCA that may present a risk to health;
complying with the new federal law and regulations requiring Unique Device Identifiers (UDI) on devices and also requiring the submission of
certain information about each device to the FDA’s Global Unique Device Identification Database; and
post-market surveillance activities and regulations, which apply when deemed by the FDA to be necessary to protect the public health or to
provide additional safety and effectiveness data for the device.
The FDA has broad regulatory compliance and enforcement powers. If the FDA determines that we failed to comply with applicable regulatory
requirements, it can take a variety of compliance or enforcement actions, which may result in any of the following sanctions:
• warning letters, untitled letters, fines, injunctions, consent decrees and civil penalties;
•
•
•
recalls, withdrawals, or administrative detention or seizure of our products or any future product candidates;
operating restrictions or partial suspension or total shutdown of production;
refusing or delaying requests for 510(k) marketing clearance or PMA approvals of new products or modified products;
• withdrawing 510(k) clearances or PMA approvals that have already been granted;
•
•
refusal to permit the export or import of our products or future product candidates; or
criminal prosecution.
In addition, other U.S. federal and state government authorities, including but not limited to the DOJ, HHS-OIG, FCC and CMS, have broad
enforcement powers and can impose various sanctions under the U.S. Anti-Kickback Statute, the U.S. False Claims Act, and various other laws. These
sanctions could include but are not limited to fines, civil penalties, criminal prosecutions, and agreements such as Deferred Prosecution Agreements or
Corporate Integrity Agreements, under which we may be required to establish additional controls to ensure compliance.
Regulation of Medical Devices in the EEA and the United Kingdom (U.K.)
Medical devices, other than active implantable medical devices (AIMDs), placed on the market in the EEA (which is comprised of the 27 Member
States of the European Union (EU) plus Norway, Liechtenstein and Iceland) must comply with the essential requirements set out in Annex I of the
Directive 93/42/EEC (Medical Devices Directive).
Separately, active implantable medical devices are governed by Directive 90/385/EEC, also known as the Active Implantable Medical Devices
Directive (AIMD Directive). AIMDs are defined as medical devices that rely on a source of electrical energy or any source of power other than that
generated by the body, which are totally or partially introduced, either surgically or medically, into the human body and intended to remain after the
procedure. Our rechargeable SNM system, or our internal product, qualifies as an AIMD and must therefore comply with the AIMD Directive, more
specifically with the essential requirements it sets out at Annex I.
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An overarching essential requirement proscribed under both the AIMD Directive and the Medical Devices Directive is that any device must be
designed and manufactured in such a way that it will not compromise the clinical condition or safety of patients, or the safety and health of users and
others. In addition, the device must achieve the performances intended by the manufacturer and be designed, manufactured and packaged in a suitable
manner.
In addition to the essential requirements set out under both the AIMD and Medical Devices Directives, the European Commission has adopted
various standards applicable to medical devices. These include standards governing common requirements, such as sterilization and safety of medical
electrical equipment, and product standards for certain types of medical devices. There are also harmonized standards relating to design and manufacture.
While not mandatory, compliance with these standards is viewed as the easiest way to satisfy the essential requirements, creating a rebuttable presumption
that the device satisfies the essential requirements.
Under the AIMD Directive, manufacturers must demonstrate compliance with the essential requirements laid down in Annex I by undergoing a
conformity assessment procedure. Conformity assessment procedures require an assessment of available clinical evidence, literature data for the product
and post-market experience in respect of similar products already marketed to ensure and declare that the products in question comply with the standards
set out in Annex I of the AIMD Directive. In addition, a conformity assessment procedure requires the intervention of a Notified Body. Notified Bodies are
separate entities that are authorized or licensed to perform such assessments by the governmental authorities of each EU Member State. Manufacturers of
AIMDs must make an application to a Notified Body for an assessment of its technical dossiers and quality system. Alternatively, manufacturers can seek
approval from the Notified Body that a representative sample of the products it has manufactured satisfies the requirements set out in the AIMD Directive
and subsequently ensure and declare that all of its products conform to the standard of the approved sample. This is also known as “type approval.”
Similar requirements for conformity assessment procedures apply under the Medical Devices Directive, which vary according to the type of
medical device and its classification. We believe that our external device is categorized as a Class IIa device under Annex IX of the Medical Devices
Directive. As such, the conformity assessment procedure requirements for our external device are identical to those detailed above for our internal product
under the AIMD Directive.
If satisfied that the AIMD or other medical device conforms to the relevant essential requirements, the Notified Body issues a certificate of
conformity, which the manufacturer uses as a basis for its own declaration of conformity (see above). The manufacturer may then apply the CE mark to the
device, which allows the device to be legally placed on and traded within the market throughout the EEA. Once the product has been placed on the market
in the EEA, the manufacturer must comply with requirements for reporting incidents and field safety corrective actions associated with the product.
In order to demonstrate safety and effectiveness for their AIMDs and other medical devices, manufacturers must conduct clinical investigations in
accordance with the requirements of Annex X to the Medical Devices Directive and Annex 7 to the AIMD Directive, as well as standards (if any) which
may be imposed by national authorities of EEA states in addition to those set out in Annex X to the Medical Devices Directive and Annex 7 to the AIMD
Directive (the Directives). Clinical studies for medical devices usually require the approval of an ethics review board and approval by or notification to the
national regulatory authorities. Both regulators and ethics committees also require the submission of serious adverse event reports during a study and may
request a copy of the final study report.
The European Parliament adopted the Medical Devices Regulation (Regulation 2017/745), which is directly applicable in the EEA. This is
intended to eliminate current differences in the regulation of medical devices among EEA countries. The Medical Devices Regulation, among other things,
is intended to establish a uniform, transparent, predictable and sustainable regulatory framework across the EEA for medical devices and ensure a high
level of safety and health while supporting innovation.
Starting January 1, 2021, all medical devices sold in the United Kingdom must meet new regulatory requirements due to the U.K.’s departure from
the EU or “Brexit.” Among other things, companies must register their devices with the U.K. Medicines & Healthcare Regulatory Agency (MHRA) and
may need to change their product marking and labeling. In addition, if the company is not based in the United Kingdom, it must appoint a
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U.K. Responsible Person to register with the MHRA and assist the company in meeting U.K. regulatory requirements.
U.S. Fraud and Abuse and Physician Payment Transparency Laws
Various U.S. federal and state laws restrict our business practices regarding items of value provided to healthcare providers including, without
limitation, the U.S. Anti-Kickback Statute, the U.S. False Claims Act, and the U.S. Physician Payments Sunshine Act.
The U.S. Anti-Kickback Statute prohibits, among other things, knowingly and willfully offering, paying, soliciting or receiving any remuneration
(including any kickback, bribe or rebate), directly or indirectly, overtly or covertly, in cash or in kind to induce or in return for purchasing, leasing, ordering
or arranging for or recommending the purchase, lease or order of any good, facility, item or service reimbursable, in whole or in part, under Medicare,
Medicaid or other federal healthcare programs. The term “remuneration” has been broadly interpreted to include anything of value, including cash, in-kind
items, meals, travel, lodging, consulting or research agreements, grants, donations, charitable contributions, free equipment or services, royalty
arrangements, stock, stock options, and the compensation derived through ownership interests.
Recognizing that the U.S. Anti-Kickback Statute is broad and may prohibit many innocuous or beneficial arrangements within the healthcare
industry, the U.S. Department of Health and Human Services has established various “safe harbors,” that if met in form and substance, will assure medical
device manufacturers, healthcare providers and other parties that they will not be prosecuted under the federal Anti-Kickback Statute. Although there are a
number of statutory exceptions and regulatory safe harbors protecting some common activities from prosecution, the exceptions and safe harbors are drawn
and interpreted narrowly. Government authorities may claim that our arrangements with physicians, hospitals and other persons or entities do not fully meet
the stringent criteria specified in these safe harbors.
Violations of the U.S. Anti-Kickback Statute may result in civil monetary penalties and can also result in criminal penalties, including criminal
fines and imprisonment. In addition, violations can result in exclusion from participation in government healthcare programs, including Medicare and
Medicaid. Government authorities may contend that we are liable under the U.S. Anti-Kickback Statute because of the intentions or actions of the parties
with whom we do business, if we acted with deliberate ignorance or reckless disregard. The majority of states also have anti-kickback laws that establish
similar prohibitions, and in some cases, may apply more broadly.
The U.S. False Claims Act prohibits, among other things, any person or entity from knowingly presenting, or causing to be presented, a false or
fraudulent claim for payment or approval to the federal government or knowingly making, using or causing to be made or used a false record or statement
material to a false or fraudulent claim to the federal government. A claim includes “any request or demand” for money or property presented to the U.S.
government. The federal civil False Claims Act also applies to false submissions that cause the government to be paid less than the amount to which it is
entitled. Intent to deceive is not required to establish liability under the civil federal civil False Claims Act, if a person acts with deliberate ignorance or
reckless disregard.
In addition, private parties may initiate “qui tam” whistleblower lawsuits against any person or entity under the U.S. False Claims Act in the name
of the government and share in the proceeds of any recovery. A violation may result in penalties and provide the basis for exclusion from federal healthcare
programs.
Additionally, the U.S. Physician Payments Sunshine Act requires annual reporting of transfers of value to certain healthcare providers by
companies whose products are reimbursable under Medicare, Medicaid or other federal healthcare programs. A manufacturer’s failure to submit timely,
accurate and complete information under the Sunshine Act may result in civil monetary penalties. Certain U.S. states similarly require tracking and
reporting of certain transfers of value to healthcare providers and some mandate implementation of commercial compliance programs or, impose
restrictions on device manufacturer marketing practices.
Anti-Bribery and Corruption Laws
Our operations outside the United States are subject to the U.S. Foreign Corrupt Practices Act (FCPA). The FCPA generally prohibits companies
and their intermediaries from engaging in bribery or making prohibited payments to foreign officials for the purpose of obtaining or retaining business or
an official government action. In addition, the FCPA imposes accounting standards and requirements on publicly traded U.S. corporations and their
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foreign affiliates, which are intended to prevent the diversion of corporate funds to the payment of bribes and other improper payments, and to prevent the
establishment of “off books” slush funds from which such improper payments can be made. We also are subject to similar anti-corruption or anti-bribery
laws in Europe, Australia, and Canada, and would be subject to such laws in many other countries in which we might choose to do business.
FCC Regulation
Because our SNM systems include a wireless radio frequency transmitter and receiver, the devices are subject to equipment authorization
requirements in the United States. The FCC requires advance clearance of all radio frequency devices before they can be imported into, sold or marketed in
the United States. These clearances ensure that the proposed products comply with FCC radio frequency emission and power level standards and will not
cause interference.
Data Privacy and Security Laws
We are also subject to various U.S. federal, state and foreign laws that protect the confidentiality and restrict the use and disclosure of personal
information, such as patient health information.
For example, the U.S. Health Insurance Portability and Accountability Act (HIPAA), as amended by the Health Information Technology for
Economic and Clinical Health Act (HITECH), establishes uniform standards governing the use and disclosure of protected health information (PHI) and
requires healthcare providers, called “covered entities”, to maintain certain safeguards to protect the privacy and security of PHI. HIPAA also requires
business associates (independent contractors or agents of covered entities that create, receive, maintain, or transmit PHI on behalf of a covered entity) to
enter into business associate agreements with the covered entity. These agreements require the business associate to safeguard the covered entity’s PHI
against improper use and disclosure.
Failure to comply with the HIPAA privacy and security standards can result in civil monetary penalties, and, in certain circumstances, criminal
penalties with fines and/or imprisonment.
HIPAA authorizes state attorneys general to file suit on behalf of their residents for violations. Courts can award damages, costs and attorneys’
fees related to violations of HIPAA in such cases. While HIPAA does not create a private right of action allowing individuals to file suit against us in civil
court for violations of HIPAA, its standards have been used as the basis for duty of care cases in state civil suits alleging negligence or recklessness in the
misuse or breach of PHI. In addition, HIPAA mandates that the Secretary of HHS conduct periodic compliance audits of HIPAA covered entities and their
business associates for compliance with the HIPAA privacy and security standards.
In the EU, we may be subject to various laws relating to our collection, control, processing and other use of personal data (i.e. data relating to an
identifiable individual). We may process personal data of our employees, our customers, and our vendors. These laws include the General Data Protection
Regulation ((EU) 2016/679) (GDPR), the E-Privacy Directive 2002/58/EC and national laws supporting aspects of the GDPR and implementing the E-
Privacy Directive. Each EU Member State has transposed the requirements laid down by the E-Privacy Directive into its own national data privacy regime,
while the GDPR permits EU Member States to implement local legislation to supplement the GDPR, and therefore the laws may differ by jurisdiction,
sometimes significantly. We need to ensure compliance with the rules in each jurisdiction where we are established or are otherwise subject to local privacy
laws.
The GDPR is directly applicable in each EU Member State, resulting in a more uniform application of data privacy laws across the EU. Like the
previous Directive, the GDPR requires that personal data may only be collected for specified, explicit and legitimate purposes based on legal bases for
processing set out in the GDPR and local laws, and may only be processed in a manner consistent with those purposes. Personal data must be secure, not be
transferred outside of the EEA unless certain steps are taken to ensure an adequate level of protection and must not be kept for longer than necessary for the
purposes of collection. In addition, the GDPR also limits the circumstances and the manner in which we are legally permitted to process that data and
transfer that data outside of the EEA. In particular, in order to process such data, explicit consent to the processing (including any transfer) is usually
required from the data subject (being the person to whom the personal data relates).
The GDPR also imposes onerous accountability obligations requiring data controllers and processors to maintain a record of their data processing.
It requires data controllers to be transparent and disclose to data subjects
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(in a concise, intelligible and easily accessible form) how their personal information is to be used, imposes limitations on retention of information,
increases requirements pertaining to pseudonymized (i.e., key-coded) data, introduces mandatory data breach notification requirements and sets higher
standards for data controllers to demonstrate that they have obtained valid consent for certain data processing activities. Fines for non-compliance with the
GDPR are significant—€20,000,000 or up to 4% of the total worldwide annual turnover of the preceding financial year, whichever is higher.
We are subject to the supervision of local data protection authorities in those jurisdictions where we are established or otherwise subject to
applicable law.
Impact of COVID-19
The COVID-19 pandemic negatively impacted our sales, starting in the second quarter of 2020 by significantly decreasing and delaying the
number of procedures performed using our rechargeable SNM system, and we expect that the pandemic or any resurgence of cases could negatively impact
our business, financial condition and results of operations. Similar to the general trend in elective and other surgical procedures, the number of procedures
performed using our rechargeable SNM system decreased significantly as healthcare organizations in the United States and globally, including in Europe
and Canada, have prioritized the treatment of patients with COVID-19 or have altered their operations to prepare for and respond to the pandemic.
Specifically, substantially all of the procedures using our rechargeable SNM system were postponed or cancelled from middle of March 2020 through May
2020, but order flow began a gradual recovery in May 2020 and continued to improve in the second half of 2020 through the second quarter of 2021.
During the second half of 2021 and through the second half of 2022, certain outpatient elective procedures were again postponed or cancelled related to the
COVID-19 pandemic and specifically the Delta and Omicron variants, which adversely affected our business during the second half of 2021 and through
the second half of 2022. While COVID-19 case volumes appear to be decreasing in the U.S. and certain other countries as a result of higher vaccination
rates, the global COVID-19 outlook remains uncertain as new variants emerge.
To protect the health of our employees, their families, and our communities, we have adapted to new and improved methods of conducting
business, including restricted access to our offices to personnel who must perform critical activities that must be completed on-site, limited the number of
such personnel that can be present at our facilities at any one time, requested that many of our employees work remotely, and implemented strict travel
restrictions. These restrictions and precautionary measures have not adversely affected our operations. Even as efforts to contain the pandemic have made
progress and some restrictions have relaxed, new variants of the virus may continue to cause additional outbreaks. The full extent of COVID-19’s effect on
our operational and financial performance will depend on future developments, including the duration, spread and intensity of the pandemic, and additional
protective measures implemented by the governmental authorities, all of which are uncertain and difficult to predict considering the rapidly evolving
landscape. However, if the pandemic continues to evolve into a long-term severe worldwide health crisis, there could be a material adverse effect on our
business, results of operations, financial condition, and cash flows.
Human Capital Resources
Workforce Overview
We take pride in our employees and the products and services we provide. We are committed to maintaining an environment that promotes job
satisfaction, respect for fellow employees, personal responsibility, and integrity in all matters. We provide a welcoming, collaborative environment that
nurtures talent and offers attractive health care and other employee benefits.
As of December 31, 2022, we had 610 employees. Of this total, 22 were employees based outside of the U.S. None of our employees is subject to
a collective bargaining agreement or represented by a trade or labor union. We consider our relationship with our employees to be good.
Our manufacturing, product development, warehouse and administrative employees are generally located in the same or adjacent facilities, which
we believe contributes to our culture of strong manufacturing, engineering and customer service capabilities.
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Inclusion, Diversity & Equity
We believe that a diverse workplace encourages creativity and a collaborative environment. We are committed to fostering an inclusive
environment, treating all employees fairly, and providing equal opportunity. As of December 31, 2022, 33 percent of our U.S. workforce is ethnically
diverse; women comprise 58 percent of our U.S. workforce; 45 percent of our manager and above employees are ethnically diverse; and 44 percent of our
manager and above employees are women.
Pay Equity
Axonics provides competitive compensation by benchmarking with other leading medical device companies, using data to adjust salary ranges
used to guide compensation decisions. We define pay as equal compensation for women, men, and all races/ethnicities who undertake the same work at the
same level, experience, and performance.
Workforce Compensation
Our compensation framework is designed to celebrate the value and contributions of our employees. We are committed to transparent
communications on compensation. Our competitive approach to compensation reflects industry benchmarks and local market standards. Our programs
include annual and long-term incentives that provide the means to share in the Company’s success. To attract the best leaders, we offer competitive benefits
and cash and equity incentives. We reward high-performing employees with an ownership stake in the company through restricted stock.
Company Information
We were incorporated in the State of Delaware in March 2012 under the name “American Restorative Medicine, Inc.” In August 2013, we
changed our name to Axonics Modulation Technologies, Inc. and in March 2021, we changed our name to Axonics, Inc. Our principal executive offices are
located at 26 Technology Drive, Irvine, California 92618 and our telephone number is 1-877-929-6642. Our website is www.axonics.com. The information
contained on or that can be accessed through our website is not incorporated by reference into this Annual Report on Form 10-K.
Available Information
Our Annual Reports on Form 10-K, Quarterly Reports on Form 10-Q, Current Reports on Form 8-K and amendments to those reports are
accessible free of charge on our website at www.axonics.com as soon as reasonably practicable after we electronically file such material with, or furnish it
to, the SEC. The SEC also maintains an internet site that contains reports, proxy and information statements and other information regarding our filings at
www.sec.gov.
Item 1A. Risk Factors.
Investing in our securities involves a high degree of risk. You should carefully consider the following information about these risks, together with the
other information appearing elsewhere in this Annual Report on Form 10-K, including our consolidated financial statements, the notes thereto and the
section entitled “Management’s Discussion and Analysis of Financial Condition and Results of Operations.” The occurrence of any of these risks could
have a material and adverse effect on our business, reputation, financial condition, results of operations and future growth prospects, as well as our ability
to accomplish our strategic objectives. Certain statements contained in this section constitute forward-looking statements. See the information included in
“Special Note Regarding Forward-Looking Statements” in this Annual Report on Form 10-K. Additional risks and uncertainties not presently known to us
or that we currently deem immaterial may also impair our business operations.
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Risks Related to Our Business and Strategy
We have incurred significant operating losses since inception, and we expect to incur operating losses in the future, and we may not be able to
achieve or sustain profitability.
We are a medical technology company with a limited commercial operating history. To date, we have invested substantially all of our efforts in the
research and development of, seeking regulatory approval for, and commercialization of our SNM systems. We are not profitable and have incurred losses
each year since we began our operations in 2013. We have a limited commercial operating history upon which to evaluate our business and prospects. We
expect that our operating expenses will continue to increase as we continue to build our commercial infrastructure, invest in research and development, and
develop, enhance, and commercialize new products. As a result, we expect to continue to incur operating losses for the foreseeable future and may never
achieve profitability. Furthermore, even if we do achieve profitability, we may not be able to sustain or increase profitability on an ongoing basis. If we do
not achieve or sustain profitability, it will be more difficult for us to finance our business and accomplish our strategic objectives, either of which would
have a material adverse effect on our business, financial condition, results of operations, and cause the market price of our common stock to decline. In
addition, failure of our systems to significantly penetrate existing or new markets would negatively affect our business, financial condition, and results of
operations.
We have not yet derived sufficient revenues to support our operations, as our activities prior to 2022 have consisted primarily of investing in our
commercial operations, developing our technology, conducting clinical studies, and developing our sales force. As a result, we have recorded net losses of
$59.7 million, $80.1 million, and $54.9 million for the years ended December 31, 2022, 2021, and 2020, respectively. As of December 31, 2022, we had an
accumulated deficit of $374.3 million. To date, we have financed our operations primarily through equity financings.
We expect that our operating expenses will continue to increase as we (i) continue to expand our commercial infrastructure, (ii) develop, enhance,
and expand the commercialization of our SNM systems in the United States, (iii) potentially seek additional FDA regulatory approvals for other future
product candidates in the United States, and (iv) increase our commercialization efforts internationally. As a result, we expect to continue to incur operating
losses for the foreseeable future. Our expected future operating losses, combined with our prior operating losses, may adversely affect the market price of
our common stock and our ability to raise capital and continue operations.
If we do not generate sufficient revenue, we may not be able to achieve profitability. Even if we do achieve profitability, we may not be able to
sustain or increase profitability in subsequent periods or on an ongoing basis. If we do not achieve or sustain profitability, it will be more difficult for us to
finance our business and accomplish our strategic objectives, either of which would have a material and adverse effect on our business, financial condition
and results of operations and cause the market price of our common stock to decline.
Our SNM systems currently represent the majority of our sales, and we are substantially dependent on the success of our SNM systems.
Until we acquired the Bulkamid product on February 25, 2021, our rechargeable SNM system was our sole product. We expect our SNM systems
to drive the majority of our sales for the foreseeable future. As a result, we are substantially dependent on its success. We expect that it will take time for us
to increase adoption of our Bulkamid products. Successfully commercializing medical devices such as ours is a complex and uncertain process. Our
commercialization efforts depend on the efforts of our management and sales team, our third-party manufacturers and suppliers, physicians and hospitals,
and general economic conditions, among other factors, including the following:
•
•
•
the effectiveness of our marketing and sales efforts in the United States and internationally;
our success in educating physicians and patients about the benefits, administration and use of our products;
the acceptance by physicians and patients of the safety and effectiveness of our products;
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•
•
•
•
•
•
our third-party manufacturers’ and suppliers’ ability to manufacture and supply the components of our SNM systems in a timely manner, in
accordance with our specifications, and in compliance with applicable regulatory requirements, and to remain in good standing with
regulatory agencies;
the availability, perceived advantages, relative cost, relative safety, and relative efficacy of alternative and competing therapies;
our ability to obtain, maintain, and enforce our intellectual property rights in and to our SNM systems;
the emergence of competing technologies and other adverse market developments, and our need to enhance our products and/or develop new
products to maintain market share in response to such competing technologies or market developments;
our ability to raise additional capital on acceptable terms, or at all, if needed to support the commercialization of our products; and
our ability to achieve and maintain compliance with all regulatory requirements applicable to our products.
We hired and trained sales representatives and clinical specialists with strong backgrounds and experience in SNM therapy and other
neurostimulation applications, and who have existing relationships with urologists and urogynecologists. However, we expect that our sales force will
require lead time in the field to grow their network of accounts and achieve the productivity levels we expect them to reach in any individual territory.
Furthermore, the use of our products will often require or benefit from direct support from us. If our sales representatives do not achieve the productivity
levels we expect them to reach, our revenue will not grow at the rate we expect and our financial performance will suffer. Also, to the extent any of our
sales force is comprised of personnel hired from our competitor, we may have to wait until applicable non-competition provisions have expired before
deploying such personnel in restricted territories or incur costs to relocate personnel outside of such territories. This may subject us to allegations that these
new hires have been improperly solicited, or that they have divulged to us proprietary or other confidential information of their former employers.
Addressing such allegations would be costly both in terms of time and resources. Any of these risks may adversely affect our business.
We rely on third parties for the manufacture of our products. This reliance on third parties increases the risk that we will not have sufficient
quantities of our products or such quantities at an acceptable cost, and reduces our control over the manufacturing process, which could delay, prevent
or impair our development or commercialization efforts.
We currently rely, and expect to continue to rely, on third-party manufacturers for the manufacture of certain components of our products. For our off-
the-shelf components, we do not have long-term supply agreements with many of our third-party manufacturers, and we purchase certain components for
our products on a purchase order basis. We may be unable to establish any agreements with third-party manufacturers or to do so on acceptable terms. Even
if we are able to establish agreements with third-party manufacturers, reliance on third-party manufacturers entails additional risks, including:
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the possible failure of the third party to manufacture any such component of our products according to our schedule, or at all, including if our
third-party contractors give greater priority to the supply of other products over ours or otherwise do not satisfactorily perform according to
the terms of the agreements and/or purchase orders between us and them;
the possible termination or nonrenewal of agreements by our third-party contractors at a time that is costly or inconvenient for us;
supplier demands for significant cost increases;
interruption of supply resulting from modifications to, or discontinuation of, a supplier’s operations;
the possible breach by the third-party manufacturers of our agreements with them;
the failure of third-party manufacturers to comply with applicable regulatory requirements;
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price fluctuations due to a lack of long-term supply arrangements with our suppliers for key components;
difficulty identifying and qualifying alternative suppliers for components in a timely manner;
the possible failure of the third-party to manufacture any such components of our products according to our specifications; and
the possible misappropriation of our proprietary information, including our trade secrets and know-how.
We do not have complete control over all aspects of the manufacturing process of, and are dependent on, our contract manufacturing partners for
compliance with current Good Manufacturing Practice (cGMP) regulations applicable to our products. Third-party manufacturers may not be able, or fail,
to comply with cGMP regulations or similar regulatory requirements outside of the United States. If our third-party manufacturers cannot successfully
manufacture material that conforms to our specifications and the strict regulatory requirements of the FDA or others, they will not be able to secure and/or
maintain marketing approval for their manufacturing facilities.
In addition, we do not have complete control over the ability of our third-party manufacturers to maintain adequate quality control, quality
assurance and qualified personnel. Although we require our third-party suppliers to supply us with components that meet our specifications and comply
with applicable provisions of the FDA’s QSR and other applicable legal and regulatory requirements in our agreements and contracts, and we perform
incoming inspection, testing or other acceptance activities to ensure the components meet our requirements, there is a risk that our suppliers will not always
act consistent with our best interests, and may not always supply components that meet our requirements or supply components in a timely manner. If the
FDA or a comparable foreign regulatory authority withdraws any such approval they have already procured, we may need to find alternative manufacturing
facilities, which would significantly impact our ability to market our products. Our failure, or the failure of our third-party manufacturers, to comply with
applicable regulations could result in sanctions being imposed on us, including fines, injunctions, civil penalties, delays, suspension or withdrawal of
approvals, license revocation, seizures or recalls, operating restrictions and criminal prosecutions, any of which could significantly and adversely harm our
business and results of operations.
Our current and anticipated future dependence upon others for the manufacture of our products may adversely affect our future profit margins and
our ability to commercialize our products on a timely and competitive basis.
We depend on single source suppliers to manufacture certain of our components, sub-assemblies and materials for our SNM systems, which
makes us vulnerable to supply shortages and price fluctuations that could have a material adverse effect on our business, financial condition and
results of operations.
We rely on single source suppliers in many instances for certain of the components, sub-assemblies and materials for our SNM systems. These
components, sub-assemblies and materials are critical and there are relatively few alternative sources of supply. We have not qualified or obtained
necessary regulatory approvals for additional suppliers for most of these components, sub-assemblies and materials, and in some instances we do not carry
a significant inventory of these items. While we believe that alternative sources of supply may be available, they may not be available if and when we need
them, or alternative suppliers may not be able to provide the quantity and quality of components and materials that we would need to manufacture our
products if our existing suppliers were unable to satisfy our supply requirements. To utilize other supply sources, we would need to identify and qualify
new suppliers to our quality standards and obtain any additional regulatory approvals required to change suppliers, which could result in manufacturing
delays and increase our expenses.
Our results of operations could be materially harmed if we are unable to accurately forecast customer demand for our products and manage
our inventory.
To ensure adequate inventory supply, we must forecast inventory needs and place orders with suppliers based on our estimates of future demand
for our products. Our ability to accurately forecast demand for our products could be negatively affected by many factors, including our failure to
adequately manage our expansion efforts, product introductions by competitors, an increase or decrease in customer demand for our products or for
products of our competitors, our failure to accurately forecast customer acceptance of new product enhancements,
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unanticipated changes in general market conditions or regulatory matters, and weakening of economic conditions or consumer confidence in future
economic conditions.
Inventory levels in excess of customer demand may result in inventory write-downs or write-offs, which would cause our gross margin to be
adversely affected and could impair the strength of our brand. Similarly, a portion of our inventory could become obsolete or expire, which could have a
material and adverse effect on our earnings and cash flows due to the resulting costs associated with inventory impairment charges and costs required to
replace obsolete inventory. Any of these occurrences could negatively impact our financial performance.
Conversely, if we underestimate customer demand for our products, we may not be able to deliver sufficient products to meet our customers’
requirements, which could result in damage to our reputation and customer relationships. In addition, if we experience a significant increase in demand,
additional supplies of raw materials or additional manufacturing capacity may not be available when required on terms that are acceptable to us, or at all, or
suppliers or our third-party manufacturers may not be able to allocate sufficient resources to meet our increased requirements, which could have an adverse
effect on our ability to meet customer demand for our products and our results of operations.
We have a limited history of manufacturing and assembling our products in commercial quantities and may encounter related problems or
delays that could result in lost revenue.
The manufacturing process of our products includes sourcing components from various third-party suppliers, assembly and testing. We must
manufacture and assemble these systems in compliance with regulatory requirements and at an acceptable cost in order to achieve and maintain
profitability. We have only a limited history of manufacturing and assembling our products and, as a result, we may have difficulty manufacturing and
assembling our products in sufficient quantities in a timely manner. Our limited manufacturing history may not provide us with enough data to accurately
predict future component demand, fluctuations in availability and pricing of commodity materials of supply, and, to anticipate our costs and supply needs
effectively. We may, in the future, experience delays in obtaining components from suppliers, which could impede our ability to manufacture and assemble
our products on our expected timeline. As a result of this or any other delays, we may encounter difficulties in production of our products, including
problems with quality control and assurance, component supply shortages or surpluses (including with respect to the ceramic and titanium we use in our
products), increased costs, shortages of qualified personnel and difficulties associated with compliance with local, state, federal and foreign regulatory
requirements.
We will need to increase the size of our organization and we may be unable to manage our growth effectively.
We have been growing rapidly in recent periods and have a relatively short history of operating as a commercial company. Any failure by us to
manage our growth effectively could have an adverse effect on our ability to achieve our development and commercialization goals.
Future growth will also impose significant added responsibilities on management, including the need to identify, recruit, train and integrate
additional employees. In addition, rapid and significant growth will place a strain on our administrative and operational infrastructure. In order to manage
our operations and growth we will need to continue to improve our operational, compliance and management controls, reporting and information
technology systems and financial internal control procedures. If we are unable to manage our growth effectively, it may be difficult for us to execute our
business strategy and our operating results and business could suffer.
We may require additional capital to finance our planned operations, which may not be available to us on acceptable terms or at all.
Our operations have consumed substantial amounts of cash since inception, primarily due to our research and development activities, conducting
clinical studies for our products, and building our dedicated direct sales organization. Our expenses have also increased substantially in connection with the
commercialization of our products in the United States, including hiring qualified personnel and retaining our sales team. We expect that certain of these
activities and the associated expenses will continue. Additional expenditures also include costs associated with manufacturing and supply, sales and
marketing costs, costs and expenses incidental to being a public company, and general operations. In addition, other unanticipated costs may arise.
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Our present and future funding requirements will depend on many factors, including:
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the costs associated with manufacturing, selling, and marketing our products, including the cost and timing of implementing our sales and
marketing plan and expanding our manufacturing capabilities;
our ability to retain and compensate the highly qualified personnel necessary to execute our plans;
our ability to effectively market and sell, and achieve sufficient market acceptance and market share for, our products;
the costs to maintain, expand, and defend the scope of our intellectual property portfolio, as well as any other action required in connection
with licensing, preparing, filing, prosecuting, defending, and enforcing any patents or other intellectual property rights, including the
Medtronic Litigation discussed under “Risks Related to Intellectual Property”;
the emergence of competing technologies and other adverse market developments, and our need to enhance our products and/or develop new
products to maintain market share in response to such competing technologies or market developments;
our ability to establish and maintain strategic licensing or other arrangements and the financial terms of such agreements;
the timing, receipt, and amount of license fees and sales of, or royalties on, or future improvements on our products, if any; and
our need to implement additional internal systems and infrastructure, including financial and reporting systems, incidental to being a public
company.
We may need to raise additional capital, and if we raise additional capital through public or private equity offerings, the ownership interest of our
existing stockholders will be diluted, and the terms of these securities may include liquidation or other preferences that adversely affect our stockholders’
rights. If we raise additional capital through debt financing, we may be subject to covenants limiting or restricting our ability to take specific actions, such
as incurring additional debt or liens, making capital expenditures or declaring dividends. If we raise additional capital through marketing and distribution
arrangements or other collaborations, strategic alliances or licensing arrangements with third parties, we may have to relinquish certain valuable rights to
our SNM systems, technologies, future revenue streams or research programs, or grant licenses on terms that may not be favorable to us. If we are unable to
obtain adequate financing when needed and on terms that are acceptable to us, we may have to delay, reduce the scope of or suspend the implementation of
our sales and marketing plan and our ongoing research and development efforts, which would have a material adverse effect on our business, financial
condition, and results of operations.
We compete against other companies offering first-, second- and third-line therapies for the treatment of OAB and SUI, including Medtronic
and Boston Scientific, respectively, some of which have longer operating histories, more established products or greater resources than we do, which
may prevent us from achieving increased market penetration and improved operating results.
We believe our SNM systems and our Bulkamid product are designed to offer several needed improvements in the SNM and bulking agent
markets for patients, physicians, and payors. However, the medical technology industry is highly competitive, subject to rapid change and significantly
affected by new product introductions and other activities of industry participants.
We consider our primary competition to be other implantable SNM devices. On SNM, we face competition from major medical device companies
worldwide, including Medtronic, the maker of InterStim X and InterStim Micro. InterStim X and InterStim Micro are currently the only other implantable
SNM devices approved for commercial sale in the United States by the FDA. Competition from Medtronic could significantly impact our ability to capture
and penetrate market share in the third-line therapy treatment market, and therefore could potentially have a material adverse effect on our business,
financial condition and results of operation.
We also compete with other less invasive third-line treatments for OAB and FI, such as BOTOX injections, a product sold by Allergan plc, PTNS,
as well as more invasive surgical treatment options, and drugs for the
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treatment of OAB and FI. In addition, emerging businesses may be in the early stages of developing additional SNM devices or therapies designed to treat
OAB or FI. Many of these companies have longer, more established operating histories and significantly greater financial, technical, marketing, sales,
distribution and other resources than we do. We face significant competition in establishing our market share in the United States and may encounter
unforeseen obstacles and competitive challenges in the United States. If one or more device manufacturers successfully develops a device that is more
effective, better tolerated or otherwise results in a better patient experience, or if improvements in other third-line therapies make them more effective,
easier to use or otherwise more attractive than our therapy, our ability to penetrate the third-line segment of the treatment market or maintain market share
could be significantly and adversely affected, which would have a material adverse effect on our business, financial condition and results of operations.
Bulkamid competes with bulking agents offered by Boston Scientific, Coloplast, and Laborie.
Our overall competitive position is dependent upon a number of factors, including:
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company, product, and brand recognition;
history of product use and physician familiarity with products and treatments;
regulatory approvals;
product safety, reliability and durability;
INS size, rechargeability and battery life;
quality and volume of clinical data;
effective marketing to and education of patients, physicians and hospitals;
product ease of use and patient comfort;
physician implantation and programming process;
sales force experience and market access;
product support and service;
technological innovation, product enhancements and speed of innovation;
pricing and revenue strategies;
procedure costs to patients and the overall healthcare system; and
dedicated practice development.
In addition to existing competitors, other larger and more established companies may acquire or in-license competitive products and could directly
compete with us. These competitors may also try to compete with our products on price both directly, through rebates and promotional programs to high
volume physicians and coupons to patients, and indirectly, through attractive product bundling with complementary products that offer convenience and an
effectively lower price compared to the total price of purchasing each product separately. Larger competitors may also be able to offer greater customer
loyalty benefits to encourage repeat use of their products and finance a sustained global advertising campaign to compete with commercialization efforts of
our SNM systems. Our competitors may seek to discredit our SNM systems by challenging our short operating history or relatively limited number of
scientific studies and publications. Additionally, certain of our competitors may challenge our intellectual property, may develop additional competing or
superior technologies and processes and compete more aggressively and sustain that competition over a longer period of time than we could. See “Risks
Related to Intellectual Property—Litigation or other proceedings or third-party claims of intellectual property infringement against us, including the
Medtronic Litigation, or any of our current or future licensors, including AMF, could require us to spend significant time and money and could prevent us
from selling our SNM systems, or affect our stock price.” Our technologies and products may be rendered obsolete or uneconomical by technological
advances or entirely different approaches developed by one or more of our competitors. As more companies develop new intellectual property in our
market, there is the possibility of a competitor acquiring patents or other rights that may limit our ability to update our technologies and products which
may impact demand for our SNM systems.
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We rely solely on Contura International A/S as a single source supplier to manufacture Bulkamid, and as such, any production or other
problems with Contura International A/S could adversely affect us.
We depend solely upon Contura International for the manufacturing of Bulkamid, pursuant to the Manufacturing and Supply Agreement. Although
alternative suppliers may exist, we are required to purchase Bulkamid exclusively from Contura International under the Manufacturing and Supply
Agreement. Additionally, finding a replacement supplier with the capabilities required to manufacture Bulkamid could take a significant amount of our
management’s time and resources, and no such additional supplier may exist. Further, obtaining the necessary FDA approvals or other qualifications under
applicable regulatory requirements and ensuring non-infringement of third-party intellectual property rights could result in a significant interruption of
supply and could require the new manufacturer to bear significant additional costs which may be passed on to us.
In addition, our reliance on Contura International entails additional risks, including reliance on Contura International for regulatory compliance
and quality assurance, the possible breach of the Manufacturing and Supply Agreement by Contura International, and the possible termination of the
Manufacturing and Supply Agreement at a time that is costly or inconvenient for us. Our failure, or the failure of Contura International, to comply with
applicable regulations could result in sanctions being imposed on us, including fines, injunctions, civil penalties, delays, suspension or withdrawal of
approvals, license revocation, seizures or recalls of products, operating restrictions and criminal prosecutions, any of which could significantly and
adversely affect supplies of Bulkamid. Our dependence on Contura International also subjects us to all of the risks related to Contura International’s
business, which are all generally beyond our control. Contura International’s ability to perform its obligations under the Manufacturing and Supply
Agreement is dependent on Contura International’s operational and financial health, which could be negatively impacted by several factors, including
changes in the economic and political and legislative conditions.
Any termination or loss of significant rights under the License Agreement would materially and adversely affect our development and
commercialization of our rechargeable SNM system.
If AMF terminates the License Agreement under certain circumstances, we may be required to pay damages to AMF and AMF may have the right to
terminate the license. In addition, if we do not have sufficient funds available to meet our payment obligations, AMF could terminate the License
Agreement. Any termination or loss of rights (including exclusivity) under the License Agreement could materially and adversely affect our ability to
develop and commercialize our rechargeable SNM system, which in turn would have a material adverse effect on our business, operating results and
prospects.
If we are not successful in converting physicians and patients to our products, our business will not succeed.
For over 20 years, physicians and patients relied on the only other approved SNM therapy offered by Medtronic, InterStim II and its predecessor,
InterStim I. As our SNM systems are relatively new products in the SNM market, our primary strategy to penetrate the market and grow our revenue is to
drive physician and patient awareness of the material benefits of our SNM systems. Physicians and patients may choose not to adopt our SNM systems for
a number of reasons, including:
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familiarity or preference for current InterStim devices or new devices that Medtronic could develop and commercialize in the future;
lack of experience with our SNM systems and with SNM as a treatment alternative;
our inability to convince key opinion leaders to provide recommendations regarding our SNM systems, or to convince physicians and patients
that it is an attractive alternative to InterStim devices and other third-line therapies such as BOTOX injections and PTNS;
perceived or actual benefits of InterStim devices;
perceived inadequacy of evidence supporting the clinical benefits or cost-effectiveness of our SNM systems over existing alternatives;
• marketing and other efforts by Medtronic targeting physicians, including those with whom they have long-term relationships; and
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ineffectiveness of our sales and marketing efforts for our SNM systems.
In addition, patients may choose not to adopt SNM therapy as a potential therapy if, among other potential reasons, their anatomy would not allow
for effective treatment with our SNM systems, they are reluctant to receive an implantable device as opposed to an alternative, non-implantable treatment,
or they are worried about potential adverse effects of SNM therapy, such as infection, discomfort from the stimulation, or soreness or weakness.
We believe that educating healthcare providers and patients about the clinical merits and patient benefits of our SNM systems as a treatment for
OAB will be key elements driving adoption of our SNM therapies. However, some physicians may have prior history with or a preference for other
treatment options. Moreover, our efforts to educate the medical community and patients on the benefits of our SNM systems will require significant
resources and we may never be successful. If healthcare providers and patients do not adopt our SNM systems, and our SNM systems do not achieve broad
market acceptance, our ability to execute our growth strategy will be impaired, and our business and future prospects may be adversely affected.
Our long-term growth substantially depends, in part, on our ability to enhance our products, and if we fail to do so we may be unable to
compete effectively.
It is important to our business and our long-term growth that we continue to enhance our SNM systems. We intend to continue to invest in
research and development activities focused on improvements and enhancements to our SNM systems.
Developing enhancements to our SNM systems can be expensive and time-consuming and could divert management’s attention away from the
commercialization of our SNM systems and divert financial resources from other operations. The success of any new product enhancements will depend on
several factors, including our ability to:
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properly identify and anticipate physician and patient needs, and develop new product enhancements to meet those needs;
demonstrate, if required, the safety and effectiveness of new enhancements to our SNM systems with data from preclinical studies and clinical
studies;
obtain, in a timely manner, the necessary regulatory clearances or approvals for new enhancements to our SNM systems, or product
modifications for our SNM systems;
avoid infringing upon the intellectual property rights of third-parties;
be fully FDA-compliant with marketing of new devices or modified products;
address competitive counter moves advanced by Medtronic to secure and maintain customers;
develop an effective and dedicated sales and marketing team to provide adequate education and training to potential users of our SNM
systems; and
receive adequate coverage and reimbursement for procedures performed with our SNM systems.
If we are not successful in commercializing our SNM systems and developing and commercializing new product enhancements, our ability to
achieve and maintain market share and increase our revenue may be impaired, which could have a material adverse effect on our business, financial
condition and results of operations.
If the quality of our products does not meet the expectations of physicians or patients, then our brand and reputation or our business could be
adversely affected.
In the course of conducting our business, we must adequately address quality issues that may arise with our products, including defects in third-
party components included in our products. Although we have established internal procedures designed to minimize risks that may arise from quality
issues, we may not be able to eliminate or mitigate occurrences of these issues and associated liabilities. In addition, even in the absence of quality issues,
we may be subject to claims and liability if the performance of our products do not meet the expectations of physicians or patients. If the quality of our
products does not meet the expectations of physicians or patients, then our brand and reputation with those physicians or patients, and our business,
financial condition and results of operations, could be adversely affected.
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The size and future growth in the market for SNM therapy and urethral bulking agents have not been established with precision and may be
smaller than we estimate. If our estimates and projections overestimate the size of this market, our sales growth may be adversely affected.
Our estimates of the size and future growth in the market for SNM therapy and urethral bulking agents, including the number of people in the
United States and Europe with symptoms of either bladder or bowel dysfunction and who are readily treatable with and eligible candidates for our therapy,
are based on a number of internal and third-party studies, reports and estimates. In addition, our internal estimates are based in large part on current
treatment patterns by healthcare providers using our therapy and our belief that the incidence of bladder and bowel dysfunction in the United States, Europe
and worldwide is increasing. While we believe these factors have historically provided and may continue to provide us with effective tools in estimating the
total market for our therapy and our SNM systems, these estimates may not be correct and the conditions supporting our estimates may change at any time,
thereby reducing the predictive accuracy of these underlying factors. The actual numbers of people with bladder or bowel dysfunction who are readily
treatable with and eligible candidates for our therapy, and the actual demand for our products or competitive products, could differ materially from our
projections if our assumptions are incorrect. As a result, our estimates of the size and future growth in the market for our products may prove to be
incorrect. If the actual number of people with bladder or bowel dysfunction who would benefit from our products and the size and future growth in the
market for our products is smaller than we have estimated, it may impair our projected sales growth and have an adverse impact on our business.
We may enter into collaborations, in-licensing arrangements, joint ventures, strategic alliances or partnerships with third-parties that may not
result in the development of commercially viable products or product improvements or the generation of significant future revenues.
In the ordinary course of our business, we may enter into collaborations, in-licensing arrangements, joint ventures, strategic alliances, partnerships
or other arrangements to develop new products or product improvements and to pursue new markets. Proposing, negotiating and implementing
collaborations, in-licensing arrangements, joint ventures, strategic alliances or partnerships may be a lengthy and complex process. Other companies,
including those with substantially greater financial, marketing, sales, technology or other business resources, may compete with us for these opportunities
or arrangements. We may not identify, secure, or complete any such transactions or arrangements in a timely manner, on a cost-effective basis, on
acceptable terms or at all. We have limited institutional knowledge and experience with respect to these business development activities, and we may also
not realize the anticipated benefits of any such transaction or arrangement. In particular, these collaborations may not result in the development of products
that achieve commercial success or viable product improvements or result in significant revenues and could be terminated prior to developing any products.
Additionally, we may not be in a position to exercise sole decision-making authority regarding the transaction or arrangement, which could create
the potential risk of creating impasses on decisions, and our future collaborators may have economic or business interests or goals that are, or that may
become, inconsistent with our business interests or goals. It is possible that conflicts may arise with our collaborators, such as conflicts concerning the
achievement of performance milestones, or the interpretation of significant terms under any agreement, such as those related to financial obligations or the
ownership or control of intellectual property developed during the collaboration. If any conflicts arise with any future collaborators, they may act in their
self-interest, which may be adverse to our best interest, and they may breach their obligations to us. In addition, we may have limited control over the
amount and timing of resources that any future collaborators devote to our or their future products. Disputes between us and our collaborators may result in
litigation or arbitration which would increase our expenses and divert the attention of our management. Further, these transactions and arrangements will be
contractual in nature and will generally be terminable under the terms of the applicable agreements and, in such event, we may not continue to have rights
to the products relating to such transaction or arrangement or may need to purchase such rights at a premium.
If we enter into in-bound intellectual property license agreements, we may not be able to fully protect the licensed intellectual property rights or
maintain those licenses. Future licensors could retain the right to prosecute and defend the intellectual property rights licensed to us, in which case we
would depend on the ability of our licensors to obtain, maintain and enforce intellectual property protection for the licensed intellectual property. These
licensors may determine not to pursue litigation against other companies or may pursue such litigation less
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aggressively than we would. Further, entering into such license agreements could impose various diligence, commercialization, royalty or other obligations
on us. Future licensors may allege that we have breached our license agreement with them, and accordingly seek to terminate our license, which could
adversely affect our competitive business position and harm our business prospects.
We may seek to grow our business through acquisitions of complementary products or technologies, and the failure to manage acquisitions, or
the failure to integrate them with our existing business, could harm our business, financial condition and operating results.
From time to time, we may consider opportunities to acquire other companies, products or technologies that may enhance our product platform or
technology, expand the breadth of our markets or customer base, or advance our business strategies. Potential acquisitions involve numerous risks,
including:
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problems assimilating the acquired products or technologies;
issues maintaining uniform standards, procedures, controls and policies;
unanticipated costs associated with acquisitions;
diversion of management’s attention from our existing business;
risks associated with entering new markets in which we have limited or no experience;
increased legal and accounting costs relating to the acquisitions or compliance with regulatory matters; and
unanticipated or undisclosed liabilities of any target.
We do not know if we will be able to identify acquisitions we deem suitable, whether we will be able to successfully complete any such
acquisitions on favorable terms or at all, or whether we will be able to successfully integrate any acquired products or technologies. Our potential inability
to integrate any acquired products or technologies effectively may adversely affect our business, operating results and financial condition.
Potential complications from our products or future enhancements to our products may not be revealed by our clinical experience.
Based on our experience, complications from use of our SNM systems may include infection, pain at site, lead migration or fracture, and the
body’s rejection of the implant. Complications of the use of Bulkamid include temporary pain, delayed urination, painful urination, and/or urinary tract
infections. If unanticipated side-effects result from the use of our products, we could be subject to liability and our device would not be widely adopted.
Long-term use may result in unanticipated complications, even after the device is removed. Additionally, while the INS batteries for our SNM systems are
designed to last approximately 15 to 20 years, we have not tested the battery in an actual implant in the body for that period and the battery may not last
that long under normal or atypical use conditions. If implants in people reveal that our battery fails before its designed life, physicians and patients may
lose confidence in our SNM systems, which may materially harm our reputation and our business.
If we fail to receive access to hospital facilities, our sales may decrease.
In the United States, in order for physicians to use our products, we expect that the hospital facilities where these physicians treat patients will
typically require us to enter into purchasing contracts. This process can be lengthy and time-consuming and requires extensive negotiations and
management time. In the EU, certain institutions may require us to engage in a contract bidding process in the event that such institutions are considering
making purchase commitments that exceed specified cost thresholds, which vary by jurisdiction. These processes are only open at certain periods of time,
and we may not be successful in the bidding process. If we do not receive access to hospital facilities via these contracting processes or otherwise, or if we
are unable to secure contracts or tender successful bids, our sales may decrease and our operating results may be harmed. Furthermore, we may expend
significant effort in these time-consuming processes and still may not obtain a purchase contract from such hospitals.
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Performance issues, service interruptions or price increases by shipping carriers could adversely affect our business and harm our reputation
and ability to provide our products on a timely basis.
Expedited, reliable shipping will be essential to our operations. We intend to rely heavily on providers of transport services for reliable and secure
point-to-point transport of our products to our customers and for tracking of these shipments. Should a carrier encounter delivery performance issues such
as loss, damage or destruction of our products, it would be costly to replace our products in a timely manner and such occurrences may damage our
reputation and lead to decreased demand for our products and increased cost and expense to our business. In addition, any significant increase in shipping
rates could adversely affect our operating margins and results of operations. Similarly, strikes, severe weather, natural disasters or other service
interruptions affecting delivery services we use would adversely affect our ability to process orders for our products on a timely basis.
Our employees, consultants, and other commercial partners may engage in misconduct or other improper activities, including non-compliance
with regulatory standards and requirements.
We are exposed to the risk that our employees, consultants, and other commercial partners and business associates may engage in fraudulent or
illegal activity. Misconduct by these parties could include intentional, reckless or negligent conduct or other unauthorized activities that violate the
regulations of the FDA and non-U.S. regulators, including those laws requiring the reporting of true, complete and accurate information to such regulators,
manufacturing standards, healthcare fraud and abuse laws and regulations in the United States and internationally or laws that require the true, complete
and accurate reporting of financial information or data. In particular, sales, marketing and business arrangements in the healthcare industry, including the
sale of medical devices, are subject to extensive laws and regulations intended to prevent fraud, misconduct, kickbacks, self-dealing and other abusive
practices. These laws and regulations may restrict or prohibit a wide range of pricing, discounting, marketing and promotion, sales commission, customer
incentive programs and other business arrangements. The precautions we take to detect and prevent this activity may not be effective in controlling
unknown or unmanaged risks or losses or in protecting us from governmental investigations or other actions or lawsuits stemming from a failure to comply
with these laws or regulations. If any such actions are instituted against us and we are not successful in defending ourselves or asserting our rights, those
actions could result in the imposition of significant fines or other sanctions, including the imposition of civil, criminal and administrative penalties,
damages, monetary fines, possible exclusion from participation in Medicare, Medicaid and other federal healthcare programs, contractual damages,
reputational harm, diminished profits and future earnings, and curtailment of operations, any of which could adversely affect our ability to operate our
business and our results of operations. Whether or not we are successful in defending against such actions or investigations, we could incur substantial
costs, including legal fees and reputational harm, and divert the attention of management in defending ourselves against any of these claims or
investigations.
Consolidation in the healthcare industry or group purchasing organizations could lead to demands for price concessions, which may affect
our ability to sell our products at prices necessary to support our current business strategies.
Healthcare costs have risen significantly over the past decade, which has resulted in or led to numerous cost reform initiatives by legislators,
regulators and third-party payors. Cost reform has triggered a consolidation trend in the healthcare industry to aggregate purchasing power, which may
create more requests for price concessions in the future. Additionally, group purchasing organizations, independent delivery networks and large single
accounts may continue to use their market power to consolidate purchasing decisions for hospitals and ambulatory surgery centers (ASCs). We expect that
market demand, government regulation, third-party coverage and reimbursement policies and societal pressures will continue to change the healthcare
industry worldwide, resulting in further business consolidations and alliances among our future customers, which may exert further downward pressure on
the prices of our products.
To successfully market and sell our products in markets outside of the United States, we must address many international business risks with
which we have limited experience, and failure to manage these risks may adversely affect our operating results and financial condition.
We have sales and operations both inside and outside the United States, including a limited sales and marketing organization outside the United
States. Our international sales strategy is to increase our presence in
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Europe, Canada, and Australia, which have established and favorable reimbursement. With the purchase of Contura, we have greatly expanded our
international operations through its direct sales force and distribution agreements. International sales and operations are subject to a number of risks,
including:
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difficulties in staffing and managing our international sales, marketing, and other operations;
increased competition as a result of more products and procedures receiving regulatory approval or otherwise being free to market in
internationally;
longer accounts receivable payment cycles and difficulties in collecting accounts receivable;
reduced or varied protection for intellectual property rights in some countries;
export restrictions, trade regulations, and foreign tax laws;
fluctuations in foreign currency exchange rates;
foreign certification and regulatory clearance or approval requirements;
difficulties in developing effective marketing campaigns in unfamiliar foreign countries;
customs clearance and shipping delays;
political, social, and economic instability internationally, terrorist attacks, and security concerns in general;
preference for locally manufactured products;
potentially adverse tax consequences, including the complexities of foreign value-added tax, tax inefficiencies related to our corporate
structure, and restrictions on the repatriation of earnings;
the burdens of complying with a wide variety of foreign laws and different legal standards;
increased financial accounting and reporting burdens and complexities; and
FCPA, Office of Foreign Assets Control (OFAC), the Bribery Act, each of which is defined below, and other export control, anti-corruption,
anti-money laundering and anti-terrorism laws and regulations.
If one or more of these risks are realized, our ability to expand our operations into international markets could be limited, which could adversely
affect our business, financial condition and results of operations.
Our ability to maintain our competitive position will depend on our ability to retain senior management and other highly qualified personnel.
Our success will depend in part on our continued ability to retain and motivate our highly qualified management, clinical, and other personnel. We
are highly dependent upon our management team, particularly our Chief Executive Officer and member of our board of directors, Raymond W. Cohen, and
the other members of our senior management, and other key personnel. Although we have entered into employment agreements with our executive officers,
each of them may terminate their employment with us at any time. The replacement of any of our key personnel would likely involve significant time and
costs and may significantly delay or prevent the achievement of our business objectives, which could have an adverse effect on our business. In addition,
we do not carry any “key person” insurance policies that could offset potential loss of service under applicable circumstances.
Many of our employees have become or will soon become vested in a meaningful amount of our common stock or common stock options. Our
employees may be more likely to leave us if the shares they own or have the option to purchase have significantly appreciated in value relative to the
original purchase price for the shares, or if the exercise prices of the options that they hold are significantly below the market price of our common stock.
Replacement of any employees who leave our company could involve significant time and costs and may significantly delay or prevent the achievement of
our business objectives, which could have an adverse effect on our business.
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If we are unable to achieve and maintain adequate levels of coverage or reimbursement for our products, our commercial success may be
severely hindered, and in the event insurers require a prior authorization process, such process may not result in positive coverage determination for
these patients.
In the United States, we derive most of our revenue from the sale of our products to hospitals and ASCs, which typically bill various third-party
payors, including Medicare, Medicaid, private insurance companies, health maintenance organizations and other healthcare-related organizations. In
addition, we expect that any portion of the costs and fees associated with our products that are not covered by these third-party payors, such as deductibles
or co-payments, will be billed directly to the patient by the provider. Further, certain third-party payors may not cover our products and the related
procedures because they may determine that our products and the related procedures are experimental or investigational. Customers that perform the
procedure may be subject to reimbursement claim denials upon submission of the claim. Customers may also be subject to recovery of overpayments if a
third-party payor makes payment for the claim and subsequently determines that the third-party payor’s coding, billing or coverage policies were not
followed. Further, any decline in the amount payors are willing to reimburse our customers could make it difficult for our customers to adopt or continue
using our products and could create additional pricing pressure for us. If we are forced to lower the price we charge for our products, our gross margins will
decrease, which could have a material adverse effect on our business, financial condition and results of operations and impair our ability to grow our
business.
Outside the United States, reimbursement levels vary significantly by country and by region, particularly based on whether the country or region
at issue maintains a single-payor system. SNM therapy is eligible for reimbursement in Canada, Australia, and certain countries in the EU, such as
Germany, France, and the United Kingdom. Annual healthcare budgets generally determine the number of SNM systems that will be paid for by the payor
in these single-payor system countries and regions. Reimbursement is obtained from a variety of sources, including government-sponsored and private
health insurance plans, and combinations of both. We intend to work with payors to obtain coverage and reimbursement approval in countries and regions
where it makes economic sense to do so, however, we may not obtain such coverage, which could have a material adverse effect on our business, financial
condition and results of operations and impair our ability to grow our business internationally.
We face the risk of product liability claims that could be expensive, divert management’s attention and harm our reputation and business. We
may not be able to maintain adequate product liability insurance.
Our business exposes us to the risk of product liability claims that are inherent in the testing, manufacturing and marketing of medical devices.
This risk exists even if a device is approved for commercial sale by the FDA and manufactured in facilities licensed and regulated by the FDA or an
applicable foreign regulatory authority. Our products are designed to affect, and any future enhancements to our products will be designed to affect,
important bodily functions and processes. Any side effects, manufacturing defects, misuse or abuse associated with our products could result in patient
injury or death. The medical technology industry has historically been subject to extensive litigation over product liability claims, and we may face product
liability suits. We may be subject to product liability claims if our products cause, or merely appear to have caused, patient injury or death. In addition, an
injury that is caused by the activities of our suppliers, such as those who provide us with components and raw materials, may be the basis for a claim
against us. Product liability claims may be brought against us by patients, healthcare providers or others selling or otherwise coming into contact with our
products, among others. If we cannot successfully defend ourselves against product liability claims, we will incur substantial liabilities and reputational
harm. In addition, regardless of merit or eventual outcome, product liability claims may result in:
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costs of litigation;
distraction of management’s attention from our primary business;
the inability to commercialize our products and develop enhancements to our products;
decreased demand for our products;
damage to our business reputation;
product recalls or withdrawals from the market;
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substantial monetary awards to patients or other claimants; or
loss of sales.
While we may attempt to manage our product liability exposure by proactively recalling or withdrawing from the market any defective products,
any recall or market withdrawal of our products may delay the supply to our customers and may impact our reputation. We may not be successful in
initiating appropriate market recall or market withdrawal efforts that may be required in the future and these efforts may not have the intended effect of
preventing product malfunctions and the accompanying product liability that may result. Such recalls and withdrawals may also be used by our competitors
to harm our reputation for safety or be perceived by patients as a safety risk when considering the use of our products, either of which could have a material
adverse effect on our business, financial condition and results of operations.
Although we have product liability and clinical study liability insurance that we believe is appropriate, this insurance is subject to deductibles and
coverage limitations. Our current product liability insurance may not continue to be available to us on acceptable terms, if at all, and, if available, coverage
may not be adequate to protect us against any future product liability claims. If we are unable to obtain insurance at an acceptable cost or on acceptable
terms or otherwise protect against potential product liability claims, we could be exposed to significant liabilities. A product liability claim, recall or other
claim with respect to uninsured liabilities or for amounts in excess of insured liabilities could have a material adverse effect on our business, financial
condition and results of operations.
We bear the risk of warranty claims on our products.
We bear the risk of warranty claims on our products. We may not be successful in claiming recovery under any warranty or indemnity provided to
us by our suppliers or third-party manufacturers in the event of a successful warranty claim against us by a customer or and any recovery from any such
supplier or third-party manufacturer could be inadequate. In addition, warranty claims brought by our customers related to third-party components may
arise after our ability to bring corresponding warranty claims against such suppliers or third-party manufacturers expires, which could result in costs to us.
Failure of a key information technology system, process, or site could have an adverse effect on our business.
We rely extensively on information technology systems to conduct our business. These systems affect, among other things, ordering and managing
materials from suppliers, shipping products to customers, processing transactions, summarizing and reporting results of operations, complying with
regulatory, legal or tax requirements, data security, and other processes necessary to manage our business. If our systems are damaged or cease to function
properly due to any number of causes, ranging from catastrophic events to power outages to security breaches, and our business continuity plans do not
effectively compensate on a timely basis, we may experience interruptions in our operations, which could have an adverse effect on our business.
Furthermore, any breach in our information technology systems could lead to the unauthorized access, disclosure and use of non-public information,
including information from our patient registry or other patient information, which is protected by HIPAA and other laws. Any such access, disclosure, or
other loss of information could result in legal claims or proceedings, liability under laws that protect the privacy of personal information, and damage to
our reputation.
If our facilities are damaged or become inoperable, we will be unable to continue to research and develop our products and, as a result, there
will be an adverse effect on our business until we are able to secure a new facility and rebuild our inventory.
We perform substantially all of our research and development and back-office activity and maintain a substantial portion of our finished goods
inventory for our SNM systems in Irvine, California. We warehouse a substantially lesser quantity of finished goods in a contract warehousing facility in
the Netherlands. Our facilities, equipment and inventory would be costly to replace and could require substantial lead time to repair or replace. Our
facilities, and those of our contractors, may be harmed or rendered inoperable by natural or man-made disasters, including, but not limited to, earthquakes,
flooding, fire and power outages, which may render it difficult or impossible for us to perform our research, development and commercialization activities
for some period of time. The inability to perform those activities, combined with the time it may take to rebuild our inventory of finished product, may
result in the loss of customers or harm to our reputation. Although we possess insurance for damage to
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our property and the disruption of our business, this insurance may not be sufficient to cover all of our potential losses and this insurance may not continue
to be available to us on acceptable terms, or at all.
Our results may be impacted by changes in foreign currency exchange rates.
As our international sales increase, we may enter into a greater number of transactions denominated in non-U.S. dollars, which could expose us to
foreign currency risks, including changes in currency exchange rates. We do not currently engage in any hedging transactions. If we are unable to address
these risks and challenges effectively, our international operations may not be successful and our business could be harmed.
We are subject to anti-bribery, anti-corruption, and anti-money laundering laws, including the U.S. FCPA, as well as export control laws,
customs laws, sanctions laws and other laws governing our operations. If we fail to comply with these laws, we could be subject to civil or criminal
penalties, other remedial measures and legal expenses, which could adversely affect our business, results of operations and financial condition.
As we grow our international presence and global operations, we will be increasingly exposed to trade and economic sanctions and other
restrictions imposed by the United States, EU, and other governments and organizations. The U.S. Departments of Justice, Commerce, State and Treasury
and other federal agencies and authorities have a broad range of civil and criminal penalties they may seek to impose against corporations and individuals
for violations of economic sanctions laws, export control laws, the FCPA and other federal statutes and regulations, including those established by the
OFAC. In addition, the U.K. Bribery Act of 2010 (the Bribery Act) prohibits both domestic and international bribery, as well as bribery across both private
and public sectors. An organization that “fails to prevent bribery” by anyone associated with the organization can be charged under the Bribery Act unless
the organization can establish the defense of having implemented “adequate procedures” to prevent bribery. Under these laws and regulations, as well as
other anti-corruption laws, anti-money laundering laws, export control laws, customs laws, sanctions laws and other laws governing our operations, various
government agencies may require export licenses, may seek to impose modifications to business practices, including cessation of business activities in
sanctioned countries or with sanctioned persons or entities and modifications to compliance programs, which may increase compliance costs, and may
subject us to fines, penalties and other sanctions. A violation of these laws or regulations would negatively affect our business, financial condition and
results of operations.
We have implemented policies and procedures designed to ensure compliance by us and our directors, officers, employees, representatives,
consultants and agents with the FCPA, OFAC restrictions, the Bribery Act and other export control, anti-corruption, anti-money-laundering and anti-
terrorism laws and regulations. Our policies and procedures may not be sufficient to ensure that our directors, officers, employees, representatives,
consultants and agents have not engaged and will not engage in conduct for which we may be held responsible, or that our business partners have not
engaged and will not engage in conduct that could materially affect their ability to perform their contractual obligations to us or even result in our being
held liable for such conduct. Violations of the FCPA, OFAC restrictions, the Bribery Act or other export control, anti-corruption, anti-money laundering
and anti-terrorism laws or regulations may result in severe criminal or civil sanctions, and we may be subject to other liabilities, which could have a
material adverse effect on our business, financial condition and results of operations.
Our ability to use our net operating losses and research and development credit carryforwards to offset future taxable income may be subject
to certain limitations.
In general, under Sections 382 and 383 of the Internal Revenue Code of 1986, as amended (the Code), a corporation that undergoes an “ownership
change,” generally defined as a greater than 50% change by value in its equity ownership over a three-year period, is subject to limitations on its ability to
utilize its pre-change net operating losses (NOLs) and its research and development credit carryforwards to offset future taxable income. Our existing
NOLs and research and development credit carryforwards may be subject to limitations arising from previous ownership changes, and if we undergo an
ownership change, our ability to utilize NOLs and research and development credit carryforwards could be further limited by Sections 382 and 383 of the
Code. In addition, our ability to deduct net interest expense may be limited if we have insufficient taxable income for the year during which the interest is
incurred, and any carryovers of such disallowed interest would be subject to the limitation rules similar to those applicable to NOLs and other attributes.
Future changes in our stock ownership, some of which might be beyond our control, could result in an ownership change under Section 382 of the Code.
For these reasons,
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in the event we experience a change of control, we may not be able to utilize a material portion of the NOLs, research and development credit
carryforwards or disallowed interest expense carryovers, even if we attain profitability.
A pandemic, epidemic or outbreak of an infectious disease in the United States or worldwide, including the outbreak of the COVID-19 virus,
could adversely affect our business.
If a pandemic, epidemic or outbreak of an infectious disease occurs in the United States or worldwide, our business may be adversely affected. In
December 2019, a novel strain of coronavirus, SARS-CoV-2, was identified in Wuhan, China. Since then, SARS-CoV-2, and the resulting disease, COVID-
19, has spread to most countries and all 50 states within the United States. The COVID-19 pandemic has negatively impacted our business, financial
condition and results of operations by significantly decreasing and delaying the number of procedures performed using our SNM systems, and we expect
the pandemic to continue to negatively impact our business, financial condition and results of operations. Similar to the general trend in elective and other
surgical procedures, the number of procedures performed using our SNM systems has decreased significantly as healthcare organizations in the United
States and globally, including in Europe and Canada, have prioritized the treatment of patients with COVID-19 or have altered their operations to prepare
for and respond to the pandemic. For example, in the United States, governmental authorities have recommended, and in certain cases required, or
healthcare providers have decided that elective, specialty and other procedures and appointments be suspended or canceled to avoid non-essential patient
exposure to medical environments and potential infection with COVID-19 and to focus limited resources and personnel capacity toward the treatment of
COVID-19 patients. We believe the COVID-19 pandemic has also negatively impacted the number of OAB, FI and UR diagnoses and patients screened for
eligibility for our SNM systems as hospitals and ASCs focus on COVID-19 and as patients postpone healthcare visits and treatments. As 2021 and 2022
progressed, we observed a diminishing degree of COVID-related impacts to our reported revenue, although we believe there continues to be some adverse
impact on our revenues. However, the extent to which the COVID-19 pandemic continues to impact our results of operations and financial condition will
depend on future developments that are highly uncertain and cannot be predicted, including new information that may emerge concerning the severity and
longevity of COVID-19 and its variants, the resurgence of COVID-19 in regions that have begun to recover from the initial impact of the pandemic, the
impact of COVID-19 on economic activity, and the actions to contain its impact on public health and the global economy. We believe this limited provider,
hospital and ASC capacity could have a significant adverse effect on our business, financial condition and results of operations following the end of the
pandemic. Additionally, even after it is deemed advisable to resume conducting elective procedures, some patients may elect not to undergo procedures or
delay scheduling procedures to avoid traveling to healthcare facilities due to safety concerns.
While the potential economic impact brought by and the duration of any pandemic, epidemic or outbreak of an infectious disease, including
COVID-19, may be difficult to assess or predict, the widespread COVID-19 pandemic has resulted in, and may continue to result in, significant disruption
of global financial markets, reducing our ability to access capital, which could in the future negatively affect our liquidity. In addition, a recession or market
correction resulting from the spread of an infectious disease, including COVID-19, could materially affect our business. Such economic recession could
have a material adverse effect on our long-term business as hospitals curtail and reduce capital and overall spending. In addition, the current economic
downturn is resulting in significant job losses and reductions in disposable income and if patients are unable to obtain or maintain health insurance policies,
this may significantly impact their ability to pay for the procedures utilizing our SNM systems, further negatively impacting our business, financial
condition and results of operations. To the extent the COVID-19 pandemic adversely affects our business and financial results, it may also have the effect
of heightening many of the other risks described herein, including those relating to incurring future operating losses, dependence on our SNM systems,
successful commercialization, supply chain and distribution channels.
The increasing focus on environmental sustainability and social initiatives could increase our costs, harm our reputation and adversely impact
our financial results.
There has been increasing public focus by investors, customers, environmental activists, the media, and governmental and nongovernmental
organizations on a variety of environmental, social and other sustainability matters. If we are not effective in addressing environmental, social and other
sustainability matters affecting our business, or setting and meeting relevant sustainability goals, our reputation and financial results may suffer. We
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may experience increased costs in order to execute upon our sustainability goals and measure achievement of those goals, which could have an adverse
impact on our business and financial condition.
In addition, this emphasis on environmental, social and other sustainability matters has resulted and may result in the adoption of new laws and
regulations, including new reporting requirements. If we fail to comply with new laws, regulations or reporting requirements, our reputation and business
could be adversely impacted.
Risks Related to Legal Matters and Government Regulation
Our operations are subject to extensive government regulation and oversight both in the United States and internationally, and our failure to
comply with applicable requirements could harm our business.
We are subject to extensive, complex, costly and evolving regulation in the United States, the United Kingdom, the EU, Canada and other
countries, including by the FDA and its foreign counterparts. With respect to medical devices, the FDA and foreign regulatory agencies regulate, among
other things, design, development and manufacturing, testing, labeling, content and language of instructions for use and storage, clinical studies, product
safety, establishment registration and device listing, marketing, sales and distribution, premarket clearance and approval, record keeping procedures,
advertising and promotion, recalls and field safety corrective actions, post-market surveillance, including reporting of deaths or serious injuries and
malfunctions that, if they were to recur, could lead to death or serious injury, post-market approval studies, and product import and export.
The regulations to which we are subject are complex and have become more stringent over time. Regulatory changes could result in restrictions on
our ability to carry on or expand our operations, higher than anticipated costs or lower than anticipated sales. Our failure to comply with all applicable
regulations could jeopardize our ability to sell our products and result in enforcement actions such as warning letters, fines, injunctions, civil penalties,
termination of distribution, recalls or seizures of products, delays in the introduction of products into the market, total or partial suspension of production,
refusal to grant clearances or approvals, withdrawals or suspensions of approvals, prohibitions on sales of our products, and in the most serious cases,
criminal penalties.
We are also subject to the periodic scheduled or unscheduled inspection of our facilities, review of production processes, and testing of our
products to confirm that we are in compliance with all applicable regulations. Adverse findings during regulatory inspections may result in costly
remediation efforts, requirements that we complete government mandated clinical studies or government enforcement actions. The manufacturers that we
work with are similarly subject to periodic scheduled or unscheduled inspections of their facilities. Adverse findings during such inspections may impact
our inventory and cause disruptions in product sales.
We may not receive the necessary clearances or approvals for modifications to our products or for future product candidates, and failure to
timely obtain necessary clearances or approvals for modifications to our products or for future product candidates would adversely affect our ability to
grow our business.
As class III medical devices, our products, and our future product candidates, are and will be subject to the most stringent degree of medical
device regulation. The research, testing, manufacturing, labeling, approval, selling, import, export, marketing and distribution of medical device products
are subject to extensive regulation by the FDA and other regulatory authorities in the United States and other countries, with regulations differing from
country to country. In the process of obtaining PMA approval, the FDA must determine that a proposed device is safe and effective for its intended use
based in part on extensive data, including, but not limited to, technical, pre-clinical, clinical trial, manufacturing and labeling data. The PMA process is
typically required for devices that are deemed to pose the greatest risk, such as life-sustaining, life-supporting or implantable devices.
In addition, a PMA generally requires the performance of one or more clinical studies. Despite the time, effort and cost, a device or modification
may not be approved or cleared by the FDA. Any modifications to our products that were not previously approved may require us to submit an additional
PMA or PMA supplement and obtain FDA approval prior to implementing the change. If the FDA requires us to go through a lengthier, more rigorous
examination, make modifications to the device, or generate additional data to submit to the FDA, future product introductions or modifications could be
delayed or canceled, which could adversely affect our ability to grow our business.
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The FDA can delay, limit or deny clearance or approval of a device for many reasons, including:
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inability to demonstrate to the satisfaction of the FDA or the applicable regulatory entity or notified body that the device is safe or effective
for its intended uses;
the disagreement of the FDA or the applicable foreign regulatory body with the design or implementation of clinical studies or the
interpretation of data from pre-clinical studies or clinical studies;
serious and unexpected adverse device effects experienced by participants in clinical studies;
the data from pre-clinical studies and clinical studies may be insufficient to support clearance or approval, where required;
inability to demonstrate that the clinical and other benefits of the device outweigh the risks;
the manufacturing process or facilities may not meet applicable requirements; and
the potential for approval policies or regulations of the FDA or applicable foreign regulatory bodies to change significantly in a manner
rendering clinical data or regulatory filings insufficient for clearance or approval.
The FDA may change its clearance and approval policies, adopt additional regulations or revise existing regulations, or take other actions, which
may impact our ability to modify our products or introduce future products on a timely basis. Such policy or regulatory changes could impose additional
requirements upon us that could delay our ability to obtain approvals, increase the costs of compliance or restrict our ability to maintain approvals once
obtained.
In order to sell our products in member countries of the EEA (which is composed of the 27 Member States of the EU plus Norway, Iceland and
Liechtenstein), it must comply with the essential requirements of the EU Active Implantable Medical Devices Directive (Council Directive 90/385/EEC)
(the AIMD Directive). If any future product candidates are also considered to qualify as an active implantable medical device, or AIMD, under the AIMD
Directive, it too will need to comply with the essential requirements it sets out. Alternatively, if a future product candidate is not considered an AIMD
under the AIMD Directive, it will still be required to comply with the essential requirements of the EU Medical Devices Directive (Council Directive
93/42/EEC). The Medical Devices Regulations (Regulation 2017/745) are also now in force, as further discussed below.
Compliance with the requirements under either of these Directives and confirmation of compliance by a Notified Body are prerequisites to
affixing the CE mark to our rechargeable SNM system and any future product candidates. Without a CE mark, medical devices cannot be sold or marketed
in the EEA. To demonstrate that our rechargeable SNM system is compliant with the essential requirements set out under the AIMD Directive, we must
undergo a conformity assessment procedure. This requires an assessment of available clinical evidence, literature data for the product and post-market
experience in respect of similar products already marketed to ensure and declare that the products in question comply with the standards set out in Annex I
of the AIMD Directive. In addition, a conformity assessment procedure requires the intervention of a Notified Body. Notified Bodies are separate entities
that are authorized or licensed to perform such assessments by the governmental authorities of each EU Member State. Manufacturers of AIMDs must
make an application to a Notified Body for an assessment of its technical dossiers and quality system. Alternatively, manufacturers can seek approval from
the Notified Body that a representative sample of the products it has manufactured satisfies the requirements set out in the AIMD Directive and
subsequently ensure and declare that all of its products conform to the standard of the approved sample. This is also known as “type approval.”
Future product candidates that are not considered AIMDs under the AIMD Directive will still require a conformity assessment procedure. The
types of procedures required are set out in the Medical Devices Directive and will vary according to the type of medical device and its classification. For
low-risk medical devices (Class I non-sterile, non-measuring devices) the manufacturer can issue a Declaration of Conformity based on a self-assessment
of the conformity of its products with the essential requirements of the EU Medical Devices Directive. However, for all other types of medical devices a
similar conformity assessment procedure to that outlined above and in the AIMD Directive will be required, also involving the intervention of a Notified
Body.
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For our products, future AIMD product candidates and all other future product candidates, the Notified Body issues a certificate of conformity
following successful completion of a conformity assessment procedure conducted in relation to the device and its manufacturer and their conformity with
the essential requirements. This certificate entitles the manufacturer to affix the CE mark to its medical devices after having prepared and signed a related
EC Declaration of Conformity.
As a general rule, demonstration of conformity of medical devices and their manufacturers with the essential requirements must be based, among
other things, on the evaluation of clinical data supporting the safety and performance of the products during normal conditions of use. Specifically, a
manufacturer must demonstrate that the device achieves its intended performance during normal conditions of use, that the known and foreseeable risks,
and any adverse events, are minimized and acceptable when weighed against the benefits of its intended performance, and that any claims made about the
performance and safety of the device are supported by suitable evidence. If we fail to remain in compliance with the applicable Directives outlined above,
we would be unable to continue to affix the CE mark to our rechargeable SNM system or our external trial system, which would prevent us from selling it
within the EEA.
Modifications to our products may require us to obtain new PMA approvals or approvals of a PMA supplement, and if we market modified
products without obtaining necessary approvals, we may be required to cease marketing or recall the modified products until required approvals are
obtained.
Certain modifications to a PMA-approved device may require approval of a new PMA or a PMA supplement, or alternatively a notification or
other submission to FDA. We will be responsible for deciding whether a modification requires approval by the FDA. However, the FDA may not agree
with our decisions regarding whether a new PMA or PMA supplement is necessary. We may make modifications to our products that we believe do not
require approval of a new PMA or PMA supplement. If the FDA disagrees with our determination and requires us to submit a new PMA or PMA
supplement for modifications to previously approved products, we may be required to cease marketing or to recall the modified product until we obtain
approval, and we may be subject to significant regulatory fines or penalties. Any delay or failure in obtaining required approvals would adversely affect our
ability to introduce enhanced products in a timely manner, which in turn would harm our future growth.
The misuse or off-label use of our products may harm our reputation in the marketplace, result in injuries that lead to product liability suits or
result in costly investigations, fines or sanctions by regulatory bodies if we are deemed to have engaged in the promotion of these uses, any of which
could be costly to our business.
The FDA and other regulatory agencies strictly regulate the marketing and promotional claims that are made about approved medical devices,
such as our products. In particular, a product may not be promoted for uses or indications that are not approved by the FDA or other similar regulatory
authorities as reflected in the product’s approved labeling. Physicians could use our products on their patients in a manner that is inconsistent with the
approved label. We cannot prevent a physician from using our products off-label when in the physician’s independent professional medical judgment he or
she deems it appropriate. There may be increased risk of injury to patients if physicians attempt to use our products off-label. Furthermore, the use of our
products for indications other than those that may be approved by the FDA or approved by any foreign regulatory body may not effectively treat such
conditions, which could harm our reputation in the marketplace among physicians and patients.
If the FDA or any foreign regulatory body determines that our promotional materials or training constitute promotion of an off-label use, it could
request that we modify our training or promotional materials or subject us to regulatory or enforcement actions, including the issuance or imposition of a
warning letter, an untitled letter, which is used for violators that do not necessitate a warning letter, injunction, seizure, civil fine or criminal penalties. It is
also possible that other federal, state or foreign enforcement authorities might take action under other regulatory authority, such as false claims laws, if they
consider our business activities to constitute promotion of an off-label use, which could result in significant penalties, including, but not limited to,
criminal, civil and administrative penalties, damages (including treble damages), fines, disgorgement, exclusion from participation in government
healthcare programs and the curtailment of our operations.
In addition, physicians may misuse our products or use improper techniques, potentially leading to adverse results, side effects or injury, which
may lead to an increased risk of product liability claims. If our products are
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misused or used with improper techniques or are determined to cause or contribute to patient harm, we may become subject to costly litigation by our
customers or patients.
The clinical study process required to obtain regulatory approvals is lengthy and expensive with uncertain outcomes. If clinical studies of our
products do not produce results necessary to support regulatory clearance or approval in the United States or elsewhere, we will be unable to expand
the indications for our products and may incur additional costs or experience delays in completing, or ultimately be unable to complete, the
commercialization of our products.
In order to obtain approval for a PMA or PMA supplement for expanded indications, the sponsor must meet the regulatory submission
requirements of the FDA, which in many cases may require a PMA applicant to conduct well-controlled clinical studies designed to assess the safety and
effectiveness of the product. Conducting clinical studies is a complex and expensive process, can take many years, and outcomes are inherently uncertain.
We incur substantial expense for, and devote significant time to, clinical studies but cannot be certain that the trials will ever result in commercial revenue.
We may experience significant setbacks in clinical studies, even after earlier clinical studies showed promising results, and failure can occur at any time
during the clinical study process. A device could malfunction or produce undesirable adverse effects that could cause us or regulatory authorities to
interrupt, delay or halt clinical studies. We, the FDA, an Institutional Review Board (IRB) or another regulatory authority may suspend or terminate clinical
studies at any time to avoid exposing trial participants to unacceptable health risks.
Successful results of pre-clinical studies are not necessarily indicative of future clinical study results, and predecessor clinical study results may
not be replicated in subsequent clinical studies. Additionally, the FDA may disagree with our interpretation of the data from our pre-clinical studies and
clinical studies, or may find the clinical study design, conduct or results inadequate to prove safety or efficacy, and may require us to pursue additional pre-
clinical studies or clinical studies.
In addition, we may estimate and publicly announce the anticipated timing of the accomplishment of various clinical, regulatory and other product
development goals, which are often referred to as milestones. These milestones could include obtaining the right to affix the CE mark to certain products in
the EU, submitting an IDE to the FDA, applying to commence a pivotal clinical study for a new product, enrolling patients in clinical studies, releasing
data from clinical studies, and other clinical and regulatory events. The actual timing of these milestones could vary dramatically compared to our estimates
and public announcements, in some cases for reasons beyond our control.
Clinical studies are necessary to support PMA applications and may be necessary to support PMA supplements for modified versions of our
products. This would require the enrollment of large numbers of suitable subjects, which may be difficult to identify, recruit and maintain as participants in
the clinical trial. Adverse outcomes in the post-approval studies could also result in restrictions or withdrawal of a PMA approval. We may need to conduct
additional clinical studies in the future for the approval of the use of our products in some foreign countries. Clinical testing is difficult to design and
implement, can take many years, can be expensive, and, testing carries uncertain outcomes. The initiation and completion of any of these studies may be
prevented, delayed, or halted for numerous reasons. We may experience a number of events that could adversely affect the costs, timing or successful
completion of our clinical studies, including:
• we may be required to submit an IDE application to FDA, which must become effective prior to commencing human clinical studies, and the
FDA may reject our IDE application and notify us that we may not begin investigational trials;
•
•
regulators and other comparable foreign regulatory authorities may disagree as to the design or implementation of our clinical studies;
regulators and/or IRBs, or other reviewing bodies may not authorize us or our investigators to commence a clinical trial, or to conduct or
continue a clinical study at a prospective or specific trial site for various reasons, including safety signals or noncompliance with regulatory
requirements;
• we may not reach agreements with prospective contract research organizations (CROs) and clinical study sites, the terms of which can be
subject to extensive negotiation and may vary significantly among different CROs and trial sites;
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•
•
•
clinical studies may produce negative or inconclusive results, and we may decide, or regulators may require us, to conduct additional clinical
studies or abandon product development programs;
the number of subjects or patients required for clinical studies may be larger than we anticipate, enrollment in these clinical studies may be
insufficient or slower than we anticipate, and the number of clinical studies being conducted at any given time may be high and result in fewer
available patients for any given clinical trial, or patients may drop out of these clinical studies at a higher rate than we anticipate;
our third-party manufacturers, including those conducting clinical studies on our behalf, may fail to comply with regulatory requirements or
meet their contractual obligations to us in a timely manner, or at all;
• we might have to suspend or terminate clinical studies for various reasons, including a finding that the subjects are being exposed to
unacceptable health risks;
• we may have to amend clinical study protocols or conduct additional studies to reflect changes in regulatory requirements or guidance, which
we may be required to submit to an IRB and/or regulatory authorities for re-examination;
•
•
the cost of clinical studies may be greater than we anticipate;
clinical sites may not adhere to the clinical protocol or may drop out of a clinical trial;
• we may be unable to recruit a sufficient number of clinical study sites;
•
•
•
regulators, IRBs, or other reviewing bodies may fail to approve or subsequently find fault with the manufacturing processes or facilities of
third-party manufacturers or suppliers of materials for our clinical studies, the materials necessary to conduct clinical studies may be
insufficient, inadequate or not available at an acceptable cost, or we may experience interruptions in supply;
approval policies or regulations of FDA or applicable foreign regulatory agencies may change in a manner rendering our clinical data
insufficient for approval; and
our products or other product candidates may have undesirable side effects or other unexpected characteristics.
Patient enrollment in clinical studies and completion of patient follow-up depend on many factors, including the size of the patient population, the
nature of the trial protocol, the proximity of patients to clinical sites, the eligibility criteria for the clinical trial, patient compliance, competing clinical
studies and clinicians’ and patients’ perceptions as to the potential advantages of the product being studied in relation to other available therapies, including
any new treatments that may be approved for the indications we are investigating. In addition, patients participating in our clinical studies may drop out
before completion of the trial or experience adverse medical events unrelated to the device. Delays in patient enrollment or failure of patients to continue to
participate in a clinical study may delay commencement or completion of the clinical trial, cause an increase in the costs of the clinical trial, or result in the
failure of the clinical trial.
Clinical studies must be conducted in accordance with the laws and regulations of the FDA and other applicable regulatory authorities’ legal
requirements, regulations or guidelines, and are subject to oversight by these governmental agencies and IRBs at the medical institutions where the clinical
studies are conducted. In addition, clinical studies must be conducted with supplies of our product produced under cGMP requirements and other
regulations. Furthermore, we rely on clinical study sites to ensure the proper and timely conduct of our clinical studies and we have limited influence over
their performance. We depend on our collaborators and on medical institutions and employees to conduct our clinical studies in compliance with good
clinical practice (GCP) requirements. If our collaborators fail to enroll participants for our clinical studies, fail to conduct the study to GCP standards or are
delayed for a significant time in the execution of trials, including achieving full enrollment, we may be affected by increased costs, program delays or both.
In addition, clinical studies that are conducted in countries outside the United States may result in additional delays and expenses due to increased shipment
costs, additional regulatory requirements and the engagement of non-U.S. resources, and may expose us to risks associated with
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clinical investigators who are unknown to the FDA, and different standards of diagnosis, screening and medical care.
Failure can occur at any stage of clinical testing. Our clinical studies may produce negative or inconclusive results, and we may decide, or
regulators may require us, to conduct additional clinical and non-clinical testing in addition to those we have planned. Our failure to adequately
demonstrate the safety and effectiveness of any product we may develop in the future would prevent receipt of regulatory clearance or approval and,
ultimately, limit our ability to commercialize the product.
Failure to comply with post-market regulatory requirements could subject us to enforcement actions, including substantial penalties, and
might require us to recall or withdraw our products from the market.
We are subject to ongoing and pervasive regulatory requirements governing, among other things, the manufacture, marketing, advertising, medical
device reporting, sale, promotion, registration, and listing of our products. For example, we are required to submit periodic reports to the FDA as a
condition of PMA approval. These reports include safety and effectiveness information about the device after its approval. Failure to submit such reports,
or failure to submit the reports in a timely manner, could result in enforcement action by the FDA. Following its review of the periodic reports, the FDA
might ask for additional information or initiate further investigation.
Regulatory changes could result in restrictions on our ability to continue or expand our operations, higher than anticipated costs, or lower than
anticipated sales. We have ongoing responsibilities under FDA regulations and applicable foreign laws and regulations. The FDA, state and foreign
regulatory authorities have broad enforcement powers. Our failure to comply with applicable regulatory requirements could result in enforcement action by
the FDA, state or foreign regulatory authorities, which may include any of the following sanctions:
•
•
•
•
•
•
untitled letters or warning letters;
fines, injunctions, consent decrees and civil penalties;
recalls, termination of distribution, administrative detention, or seizure of our products;
customer notifications or repair, replacement or refunds;
operating restrictions or partial suspension or total shutdown of production;
delays in or refusal to grant future PMA approvals or foreign regulatory approvals of future product candidates, new intended uses, or
modifications to our existing product;
• withdrawals or suspensions of PMAs or foreign regulatory approvals, resulting in prohibitions on sales of our products;
•
•
FDA refusal to issue certificates to foreign governments needed to export products for sale in other countries; and
criminal prosecution.
Any of these sanctions could result in higher than anticipated costs or lower than anticipated sales and have a material adverse effect on our
reputation, business, financial condition and results of operations.
Our products must be manufactured in accordance with federal and state regulations, and we or any of our suppliers or third-party
manufacturers could be forced to recall our products or terminate production if we fail to comply with these regulations.
The methods used in, and the facilities used for, the manufacture of our products must comply with the QSR, which is a complex regulatory
scheme that covers the procedures and documentation of the design, testing, production, process controls, quality assurance, labeling, packaging, handling,
storage, distribution, installation, servicing and shipping of medical devices. Furthermore, we are required to verify that our suppliers maintain facilities,
procedures and operations that comply with our quality standards and applicable regulatory requirements. The FDA enforces the QSR through periodic
announced or unannounced inspections of medical device manufacturing facilities, which may include the facilities of subcontractors. Our products are also
subject to similar state regulations and various laws and regulations of foreign countries governing manufacturing.
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Our third-party manufacturers may not take the necessary steps to comply with applicable regulations, which could cause delays in the delivery of
our products or result in it being adulterated or misbranded under the Federal Food, Drug, and Cosmetic Act. In addition, failure to comply with applicable
FDA requirements or later discovery of previously unknown problems with the manufacturing processes for our products could result in, among other
things: warning letters or untitled letters, fines, injunctions or civil penalties, suspension or withdrawal of approvals, seizures or recalls of our products,
total or partial suspension of production or distribution, administrative or judicially imposed sanctions, the FDA’s refusal to grant pending or future
clearances or approvals, clinical holds, refusal to permit the import or export of our products, and criminal prosecution of us or our employees. Any of
these actions could significantly and negatively affect supply of our products. If any of these events occurs, our reputation could be harmed, we could be
exposed to product liability claims and we could lose customers and experience reduced sales and increased costs.
If treatment guidelines for OAB, SUI, FI or UR change or the standard of care evolves, we may need to redesign and seek a new marketing
authorization from the FDA for our products.
If treatment guidelines for OAB, SUI, FI or UR change or the standard of care evolves, we may need to redesign our products, or any future
product, and seek new approvals from the FDA. PMA approvals from the FDA are based on current treatment guidelines at the time of the approvals. If
treatment guidelines change so that different treatments become desirable, the clinical utility of our products could be diminished and our business could be
adversely affected.
Our products may cause or contribute to adverse medical events or be subject to failures or malfunctions that we are required to report to the
FDA, and if we fail to do so, we would be subject to sanctions that could harm our reputation, business, financial condition and results of operations.
We are subject to the FDA’s medical device reporting regulations and similar foreign regulations, which require us to report to the FDA when we
receive or become aware of information that reasonably suggests that our products may have caused or contributed to a death or serious injury or
malfunctioned in a way that, if the malfunction were to recur, it could cause or contribute to a death or serious injury. The timing of our obligation to report
is triggered by the date we become aware of the adverse event as well as the nature of the event. We may fail to report adverse events of which we become
aware within the prescribed timeframe. We may also fail to recognize that we have become aware of a reportable adverse event, especially if it is not
reported to us as an adverse event or if it is an adverse event that is unexpected or removed in time from the use of the product. If we fail to comply with
our reporting obligations, the FDA could take action, including warning letters, untitled letters, administrative actions, criminal prosecution, imposition of
civil monetary penalties, revocation of device approvals, seizure of our products or delay in clearance or approval of modifications to our products.
The FDA and foreign regulatory bodies have the authority to require the recall of commercialized products in the event of material deficiencies or
defects in design or manufacture of a product or in the event that a product poses an unacceptable risk to health. The FDA’s authority to require a recall
must be based on a finding that there is reasonable probability that our products could cause serious injury or death. We may also choose to voluntarily
recall our products if any material deficiency is found. A government-mandated or voluntary recall by us could occur as a result of an unacceptable risk to
health, component failures, malfunctions, manufacturing defects, labeling or design deficiencies, packaging defects or other deficiencies or failures to
comply with applicable regulations. Defects or other errors in our products may occur in the future. Depending on the corrective action we take to redress
deficiencies or defects, the FDA may require, or we may decide, that we will need to obtain new approvals for our products before we may market or
distribute the corrected device. Seeking such approvals may delay our ability to replace the recalled devices in a timely manner. Moreover, if we do not
adequately address problems associated with our products, we may face additional regulatory enforcement action, including FDA warning letters, product
seizure, injunctions, administrative penalties or civil or criminal fines.
Companies are required to maintain certain records of recalls and corrections, even if they are not reportable to the FDA. We may initiate
voluntary withdrawals or corrections for our products in the future that we may determine do not require notification of the FDA. If the FDA disagrees with
our determinations, it could require us to report those actions as recalls and we may be subject to enforcement action. A future recall announcement could
harm our reputation with customers, potentially lead to product liability claims against us and negatively affect our sales. Any corrective action, whether
voluntary or involuntary, as well as defending ourselves in a lawsuit,
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will require the dedication of our time and capital, distract management from operating our business and may harm our reputation and financial results.
Additionally, if we or others identify undesirable side effects, or other previously unknown problems, caused by our products, a number of
potentially negative consequences could result, including:
•
•
•
•
regulatory authorities may withdraw their approval of the product;
regulatory authorities may require a recall of the product or we may voluntarily recall a product;
regulatory authorities may require the addition of warnings or contraindications in the product labeling, narrowing of the indication in the
product label or issuance of field alerts to physicians and pharmacies;
regulatory authorities may require us to create a guide outlining the risks of such side effects for distribution to patients;
• we may be subject to limitations as to how we promote the product;
• we may be required to change the way the product is administered or modify the product in some other way;
•
•
regulatory authorities may require additional clinical studies or costly post-marketing testing and surveillance to monitor the safety or efficacy
of the product;
sales of the product may decrease significantly;
• we could be sued and held liable for harm caused to patients; and
•
our brand and reputation may suffer.
Any of the above events could prevent us from achieving or maintaining market acceptance of our products and could substantially increase the
costs of commercializing our products. The demand for our products could also be negatively impacted by any adverse effects of a competitor’s product or
treatment.
Legislative or regulatory reforms in the United States or Europe may make it more difficult and costly for us to obtain regulatory clearances or
approvals for modifications to our products, or to manufacture, market or distribute our products.
From time to time, legislation is drafted and introduced in U.S. Congress that could significantly change the statutory provisions governing the
regulation of medical devices. In addition, FDA regulations and guidance are often revised or reinterpreted by the FDA in ways that may significantly
affect our business and products. Any new statutes, regulations or revisions or reinterpretations of existing regulations may impose additional costs or
lengthen review times, or make it more difficult to obtain approval for additional indications for, manufacture, market or distribute our products. We cannot
determine what effect changes in regulations, statutes, legal interpretation or policies, when and if promulgated, enacted or adopted may have on our
business in the future. Such changes could, among other things, require: additional testing prior to obtaining clearance or approval for future product
candidates, changes to manufacturing methods, recall, replacement or discontinuance of future product candidates, or additional record keeping.
We are subject to certain federal, state and foreign fraud and abuse laws, health information privacy and security laws and transparency laws,
which, if violated, could subject us to substantial penalties. Additionally, any challenge to or investigation into our practices under these laws could
cause adverse publicity and be costly to respond to, and thus could harm our business.
There are numerous U.S. federal and state, as well as foreign, laws pertaining to healthcare fraud and abuse, including anti-kickback, false claims
and physician transparency laws. Our business practices and relationships with providers are subject to scrutiny under these laws. We may also be subject
to privacy and security regulation related to patient, customer, employee and other third-party information by both the federal government and the states
and
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foreign jurisdictions in which we conduct our business. The healthcare laws and regulations that may affect our ability to operate include, but are not
limited to:
•
•
•
the federal Anti-Kickback Statute, which prohibits, among other things, persons and entities from knowingly and willfully soliciting, offering,
receiving or providing remuneration, directly or indirectly, in cash or in kind, to induce either the referral of an individual or furnishing or
arranging for a good or service, for which payment may be made, in whole or in part, under federal healthcare programs, such as Medicare
and Medicaid;
the federal civil and criminal false claims laws and civil monetary penalties laws, including the federal civil False Claims Act, which prohibit,
among other things, individuals or entities from knowingly presenting, or causing to be presented, claims for payment from Medicare,
Medicaid or other federal healthcare programs that are false or fraudulent;
the federal Civil Monetary Penalties Law, which prohibits, among other things, offering or transferring remuneration to a federal healthcare
beneficiary that a person knows or should know is likely to influence the beneficiary’s decision to order or receive items or services
reimbursable by the government from a particular provider or supplier;
• HIPAA which created additional federal criminal statutes that prohibit, among other things, executing a scheme to defraud any healthcare
benefit program and making false statements relating to healthcare matters;
•
the federal Physician Sunshine Act under the Patient Protection and Affordable Care Act, as amended by the Health Care and Education
Reconciliation Act, collectively referred to as the Affordable Care Act, which requires reports annually to the CMS information related to
payments and other transfers of value to physicians;
• HIPAA, as amended by the Health Information Technology for Economic and Clinical Health Act of 2009 (HITECH Act) and their respective
implementing regulations, which impose requirements on certain covered healthcare providers, health plans and healthcare clearinghouses as
well as their business associates that perform services for them that involve individually identifiable health information, relating to the
privacy, security and transmission of individually identifiable health information without appropriate authorization, including mandatory
contractual terms as well as directly applicable privacy and security standards and requirements;
•
analogous state and foreign law equivalents of each of the above federal laws, such as anti-kickback and false claims laws which may apply to
items or services reimbursed by any third-party payor, including commercial insurers or patients; state laws that require device companies to
comply with the industry’s voluntary compliance guidelines and the applicable compliance guidance promulgated by the federal government
or otherwise restrict payments that may be made to healthcare providers and other potential referral sources; state laws that require device
manufacturers to report information related to payments and other transfers of value to physicians and other healthcare providers or marketing
expenditures; consumer protection and unfair competition laws, which broadly regulate marketplace activities and activities that potentially
harm customers; and
•
state laws related to insurance fraud in the case of claims involving private insurers.
These laws and regulations, among other things, constrain our business, marketing and other promotional activities by limiting the kinds of
financial arrangements, including sales programs, we may have with hospitals, physicians or other potential purchasers of our products. Due to the breadth
of these laws, the narrowness of statutory exceptions and regulatory safe harbors available, and the range of interpretations to which they are subject, it is
possible that some of our current or future practices might be challenged under one or more of these laws.
To enforce compliance with the healthcare regulatory laws, certain enforcement bodies have recently increased their scrutiny of interactions
between healthcare companies and healthcare providers, which has led to a number of investigations, prosecutions, convictions and settlements in the
healthcare industry. Responding to investigations can be time- and resource-consuming and can divert management’s attention from the business.
Additionally, as a result of these investigations, healthcare providers and entities may have to agree to additional
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compliance and reporting requirements as part of a consent decree or corporate integrity agreement. Any such investigation or settlement could increase our
costs or otherwise have an adverse effect on our business. Even an unsuccessful challenge or investigation into our practices could cause adverse publicity,
and responding to any such challenge or investigation would be costly and divert the attention of our management. If our operations are found to be in
violation of any of the healthcare laws or regulations described above or any other healthcare regulations that apply to us, we may be subject to penalties,
including administrative, civil and criminal penalties, damages, fines, exclusion from participation in government healthcare programs, such as Medicare
and Medicaid, imprisonment, contractual damages, reputational harm, disgorgement and the curtailment or restructuring of our operations.
We may be subject to, or may in the future become subject to, U.S. federal and state, and foreign laws and regulations imposing obligations on
how we collect, store and process personal information. Our actual or perceived failure to comply with such obligations could harm our business.
Ensuring compliance with such laws could also impair our efforts to maintain and expand our customer base, and thereby decrease our revenue.
As described above, in the conduct of our business, we may at times process personal data, including health-related personal data. The U.S. federal
government and various states have adopted or proposed laws, regulations, guidelines and rules for the collection, distribution, use and storage of personal
information of individuals. We may also be subject to U.S. federal rules, regulations and guidance concerning data security for medical devices, including
guidance from the FDA. State privacy and security laws vary from state to state and, in some cases, can impose more restrictive requirements than U.S.
federal law. Where state laws are more protective, we must comply with the stricter provisions. In addition to fines and penalties that may be imposed for
failure to comply with state law, some states also provide for private rights of action to individuals for misuse of personal information.
The EU also has laws and regulations dealing with the collection, use and processing of personal data obtained from individuals in the EU, which
are often more restrictive than those in the United States and which restrict transfers of personal data to the United States unless certain requirements are
met. These obligations may be interpreted and applied in a manner that is inconsistent from one jurisdiction to another and may conflict with other
requirements or our practices.
Any actual or perceived failure by us or the third parties with whom we work to comply with privacy or security laws, policies, legal obligations
or industry standards, or any security incident that results in the unauthorized release or transfer of personally identifiable information, may result in
governmental enforcement actions and investigations including by European Data Protection Authorities and U.S. federal and state regulatory authorities,
fines and penalties, litigation and/or adverse publicity, including by consumer advocacy groups, and could cause our customers, their patients and other
healthcare professionals to lose trust in us, which could harm our reputation and have a material adverse effect on our business, financial condition and
results of operations.
Our business involves the use of hazardous materials and our third-party manufacturers must comply with environmental laws and
regulations, which may be expensive and restrict how we do business.
Our third-party manufacturers’ activities may involve the controlled storage, use and disposal of hazardous materials. Our manufacturers are
subject to federal, state, local and foreign laws and regulations governing the use, generation, manufacture, storage, handling and disposal of these
hazardous materials. We currently carry no insurance specifically covering environmental claims relating to the use of hazardous materials. Although we
believe the safety procedures of our manufacturers for handling and disposing of these materials and waste products comply with the standards prescribed
by these laws and regulations, we cannot eliminate the risk of accidental injury or contamination from the use, storage, handling or disposal of hazardous
materials. In the event of an accident, state or federal or other applicable authorities may curtail our manufacturers’ use of these materials and interrupt their
business operations which could adversely affect our business.
Compliance with securities rules relating to “conflict minerals” may require us and our suppliers to incur substantial expense and may result
in disclosure by us that certain minerals used in products we manufacture or contract to manufacture are not “DRC conflict free.”
Because we manufacture or contract to manufacture a product that contains titanium, we may be required under rules promulgated by the SEC
governing disclosure of the use of “conflict minerals” (tin, tungsten, tantalum and gold) to determine whether those minerals are necessary to the
functionality or production of our SNM systems
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and, if so, conduct a country of origin inquiry with respect to all such minerals. If any such minerals may have originated in the Democratic Republic of the
Congo (DRC) or any of its adjoining countries, or covered countries, then we must conduct diligence on the source and chain of custody of those conflict
minerals to determine if they originated in one of the covered countries and, if so, whether they financed or benefited armed groups in the covered
countries. Disclosures relating to the products that may contain conflict minerals, the country of origin of those minerals and whether they are “DRC
conflict free” must be provided in a Form SD (and accompanying conflict minerals report, if required, to disclose the diligence undertaken by us in
sourcing the minerals and our conclusions relating to such diligence). If we are required to submit a conflict minerals report, that report must be audited by
an independent auditor pursuant to existing government auditing standards. Compliance with this disclosure rule may be very time-consuming for our
management and personnel (as well as time-consuming for our suppliers) and could involve the expenditure of significant amounts of money by us and
them. Disclosures mandated by this rule, which can be perceived by the market to be “negative,” may cause customers to refuse to purchase our SNM
systems. The cost of compliance with the rule could adversely affect our results of operations.
We depend upon third-party suppliers, including single source component suppliers, making us vulnerable to supply problems, which could
lead to requiring new regulatory approvals in order to make component or supplier changes.
We rely on third-party suppliers, including some single source suppliers for certain components of our products, to provide us with a portion of our
demand for one of our products as well as components used in the manufacturing of our products. In some cases, we purchase supplies through purchase
orders and do not have long-term supply agreements with, or guaranteed commitments from, our component suppliers, including single source suppliers.
Many of our suppliers and contract manufacturers are not obligated to perform services or supply products for any specific period, in any specific quantity
or at any specific price, except as may be provided in a particular purchase order. We depend on our suppliers to provide us and our customers with
materials or products in a timely manner that meet our and their quality, quantity and cost requirements. These suppliers may encounter problems during
manufacturing for a variety of reasons, including as a result of the ongoing COVID-19 pandemic, any of which could delay or impede their ability to meet
our demand. These suppliers may cease producing the products or components we purchase from them or otherwise decide to cease doing business with us.
Further, we maintain limited volumes of inventory from most of our suppliers and contract manufacturers. If we inaccurately forecast demand for finished
goods, we may be unable to meet customer demand which could harm our competitive position and reputation. In addition, if we fail to effectively manage
our relationships with our suppliers and contract manufacturers, we may be required to change suppliers or contract manufacturers. While we believe
alternate suppliers exist for all materials, components and services necessary to manufacture our products, establishing additional or replacement suppliers
for any of these materials, components or services, if required, could be time-consuming, expensive and may result in interruptions in our operations and
product delivery. Even if we are able to find replacement suppliers, we will be required to verify that the new supplier maintains facilities, procedures and
operations that comply with our quality expectations and applicable regulatory requirements. Any of these events could require that we obtain a new
regulatory authority approval before we implement the change, which could result in further delay or which may not be obtained at all. If our third-party
suppliers fail to deliver the required commercial quantities of materials on a timely basis and at commercially reasonable prices, and we are unable to find
one or more replacement suppliers capable of production at a substantially equivalent cost, volumes and quality on a timely basis, the continued
commercialization of our products, the supply of our products to customers and the development of any future products will be delayed, limited or
prevented, which could have material adverse effect on our business, financial condition and results of operations.
Risks Related to Intellectual Property
Litigation or other proceedings or third-party claims of intellectual property infringement against us, including the Medtronic Litigation, or
any of our current or future licensors, including AMF, could require us to spend significant time and money and could prevent us from selling our
products, or affect our stock price.
Our commercial success will depend in part on our ability to avoid infringement of the proprietary rights of third parties. To the extent that our
commercial partners, collaborators, employees and consultants use intellectual property owned by others in their work for us, disputes may arise as to the
rights in related or resulting know-how and inventions. Our competitors in both the United States and internationally, many of which have substantially
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greater resources, and, may have made substantial investments in patent portfolios and competing technologies, may have applied for or obtained or may in
the future apply for and obtain, patents that will prevent, limit or otherwise interfere with our ability to make, use and sell our products. We do not always
conduct independent reviews of patents issued to third parties. Because we have not conducted a formal freedom to operate analysis for patents related to
our products, we may not be aware of issued patents that a third party might assert are infringed by one of our current or future product candidates, which
could materially impair our ability to commercialize our products. Even in the event that we conduct a formal freedom to operate analysis, patent searches
to determine whether our products infringe patents held by third parties are inherently uncertain and such searches cannot assure that all relevant patents are
identified. In addition, patent applications in the United States and elsewhere can be pending for many years before issuance, or unintentionally abandoned
patents or applications can be revived, so there may be applications for other patents now pending or recently revived patents of which we are unaware that
our products may infringe. There may also be patent applications that have been filed but not published that, when issued as patents, could be asserted
against us. There is a substantial amount of litigation, both within and outside the United States, involving patent and other intellectual property rights in
the technology and medical device industries, including patent infringement lawsuits, interferences, oppositions and inter partes reexamination or review
proceedings before the U.S. Patent and Trademark Office. Numerous U.S. and foreign issued patents and pending patent applications, which are owned by
third parties, exist in the fields in which we are developing our products or will develop future product candidates. As the technology and medical device
industries expand and more patents are issued, the risk continues, or possibly increases, that our products may be subject to claims of infringement of the
patent rights of third parties.
Third parties may assert that we, or any of our current or future licensors, including AMF, are employing their proprietary technology without
authorization. For example, on November 4, 2019, Medtronic, Inc., Medtronic Puerto Rico Operations Co., Medtronic Logistics LLC and Medtronic USA,
Inc. (collectively, the Medtronic Affiliates) filed a complaint against us in the U.S. District Court for the Central District of California, Case No. 8:19-cv-
2115, and amended the complaint on November 26, 2019. We refer to this matter as the Medtronic Litigation. The complaint asserts that our rechargeable
SNM system infringes U.S. Patent Nos. 8,036,756, 8,626,314, 9,463,324 and 9,821,112 held by the Medtronic Affiliates, and the amended complaint
further includes the additional patents 8,738,148; 8,457,758; and 7,774,069 (collectively, the Medtronic Patents). The Medtronic Litigation requests
customary remedies for patent infringement, including (i) a judgment that we have infringed and are infringing the Medtronic Patents, (ii) damages,
including treble damages for willful infringement, (iii) a permanent injunction preventing us from infringing the Medtronic Patents, (iv) attorneys’ fees, and
(v) costs and expenses. We believe the allegations are without merit and are vigorously defending ourselves against them. We are unable to predict the
likelihood of success of the claims of the Medtronic Affiliates against us or to quantify any risk of loss. The Medtronic Litigation could last for an extended
period of time and require us to dedicate significant financial resources and management resources to our defense. An adverse ruling against us could
materially and adversely affect our business, financial position, results of operations or cash flows and could also result in reputational harm. Even if we are
successful in defending against these claims, the Medtronic Litigation could result in significant costs, delays in future product developments, reputational
harm or other collateral consequences. The Company is currently engaged in discovery in the Medtronic Litigation. A jury trial is scheduled in the
Medtronic Litigation for April 2023.
Defense of any of the above claims, including the Medtronic Litigation, would require us to dedicate substantial time and resources, which time
and resources could otherwise be used by us toward the maintenance of our own intellectual property and the commercialization of our products, or by any
of our current or future licensors for operational upkeep and manufacturing of our products.
The legal threshold for initiating litigation or contested proceedings may be low, so that even lawsuits or proceedings with a low probability of
success might be initiated. Litigation and contested proceedings can also be expensive and time-consuming, and our adversaries in these proceedings may
have the ability to dedicate substantially greater resources to prosecuting these legal actions than we can. We may also occasionally use these proceedings
to challenge the patent rights of others.
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Any lawsuits resulting from such allegations could subject us to significant liability for damages and invalidate our proprietary rights. Any
potential intellectual property litigation also could force us to do one or more of the following:
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stop making, selling or using products or technologies that allegedly infringe the asserted intellectual property;
lose the opportunity to license our technology to others or to collect royalty payments based upon successful protection and assertion of our
intellectual property rights against others;
incur significant legal expenses;
pay substantial damages or royalties to the party whose intellectual property rights we may be found to be infringing;
pay the attorney’s fees and costs of litigation to the party whose intellectual property rights we may be found to be infringing;
redesign those products that contain the allegedly infringing intellectual property, which could be costly, disruptive, or infeasible; and
attempt to obtain a license to the relevant intellectual property from third parties, which may not be available on reasonable terms, or at all, or,
from third parties whom may attempt to license rights that they have or do not have.
Any litigation or claim against us or AMF, even those without merit, may cause us to incur substantial costs, and could place a significant strain on
our financial resources, divert the attention of management from commercialization of our SNM systems, or harm our reputation. If we or AMF are found
to infringe the intellectual property rights of third parties, we could be required to pay substantial damages (which may be increased up to three times of
awarded damages) and/or substantial royalties and could be prevented from selling our infringing products unless we obtain a license or are able to
redesign our SNM systems to avoid infringement. Any such license may not be available on reasonable terms, if at all, and we may not be able to redesign
the infringing product in a way that would not infringe the intellectual property rights of others. We could encounter delays in product introductions while
we attempt to develop alternative methods or products. If we fail to obtain any required licenses or make any necessary changes to our SNM systems,
including future technologies, we may have to withdraw our SNM systems from the market or may be unable to commercialize our SNM systems.
In addition, third parties may assert infringement claims against our customers. These claims may require us to initiate or defend protracted and
costly litigation on behalf of our customers or indemnify our customers for any costs associated with their own initiation or defense of infringement claims,
regardless of the merits of these claims. If any of these claims succeed or settle, we may be forced to pay damages or settlement payments on behalf of our
customers or may be required to obtain licenses for the products they use. If we cannot obtain all necessary licenses on commercially reasonable terms, our
customers may be forced to stop using our products.
If we or any of our current or future licensors, including AMF, are unable to maintain, obtain or adequately protect our intellectual property
rights, we may not be able to compete effectively in our market or we could be required to incur significant expenses to enforce or defend our rights or
attempt to do the same.
Our commercial success depends in part on ours and any of our current or future licensors’, including AMF’s, success in obtaining, maintaining
and protecting patents, trademarks, trade secrets and other intellectual property rights and proprietary technology in the United States and elsewhere. If we
or any of our current or future licensors, including AMF, do not adequately protect our respective intellectual property and proprietary technology,
competitors may be able to use our technologies and erode or negate any competitive advantage we may have, which could harm our business and ability to
achieve profitability.
Our intellectual property coverage includes protection provided by patents and other intellectual property licensed through the License Agreement
with AMF. We rely on AMF to maintain the patents and otherwise protect the intellectual property we license from them. If in the future we no longer have
rights to one or more of these licensed patents or other licensed intellectual property, our intellectual property coverage may be compromised, which in turn
could affect our ability to protect our rechargeable SNM system and defend it against competitors.
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Our patents may not have, and any of our pending patent applications that mature into issued patents may not include, claims with a scope
sufficient to adequately protect our products, or any additional features we develop for our products or any new products. Other parties may have
developed technologies that may be related to or competitive with our products, and, may have filed, or may file, patent applications, and, may have
received, or may receive patents, that overlap or conflict with our patent applications, either by claiming the same methods or devices or by claiming
subject matter that could dominate our patent position. The patent positions of medical device companies, including our patent position, may involve
complex legal and factual questions, and therefore, the scope, validity and enforceability of any patent claims that we may obtain cannot be predicted with
certainty. Patents, if issued, may be challenged, deemed unenforceable, invalidated or circumvented. Proceedings challenging our patents could result in
either loss of the patent, or denial of the patent application or loss or reduction in the scope of one or more of the claims of the patent or patent application.
In addition, such proceedings may be costly. Thus, any patents that we may own may not provide any protection against competitors. Furthermore, an
adverse decision may result in a third party receiving a patent right sought by us, which in turn could affect our ability to commercialize our products.
Though an issued patent is presumed valid and enforceable, its issuance is not conclusive as to its validity or its enforceability and it may not
provide us with adequate proprietary protection or competitive advantages against competitors with similar products. Competitors could purchase our
products and attempt to replicate some or all of the competitive advantages we derive from our development efforts, circumvent or design around our
patents, or develop and obtain patent protection for more effective technologies, designs or methods. We may be unable to prevent the unauthorized
disclosure or use of our technical knowledge or trade secrets by consultants, suppliers, vendors, former employees and current employees. In addition, third
parties may create new products or methods that achieve similar results without infringing upon patents we own. If these developments were to occur, it
could have an adverse effect on our sales or market position. The laws of some foreign countries do not protect our proprietary rights to the same extent as
the laws of the United States, and we may encounter significant problems in protecting our proprietary rights in these countries.
Our ability to enforce our patent rights depends on our ability to detect infringement. It may be difficult to detect infringers who do not advertise
the components that are used in their products. In addition, it may be difficult or impossible to obtain evidence of infringement in a competitor’s or
potential competitor’s product. We may not prevail in some, or any lawsuits that we initiate and the damages or other remedies awarded if we were to
prevail may not be commercially meaningful. Any litigation to enforce or defend our patent rights, even if we were to prevail, could be costly and time-
consuming and could divert the attention of our management and key personnel from our business operations.
In addition, proceedings to enforce or defend our patents could put our patents at risk of being invalidated, held unenforceable, or interpreted
narrowly. Such proceedings could also provoke third parties to assert claims against us, including that some, or all, of the claims in one or more of our
patents are invalid or otherwise unenforceable. If any of our patents covering our products are invalidated or found unenforceable, or, if a court found that
valid, enforceable patents held by third parties covered our products, our competitive position could be harmed, or, we could be required to incur significant
expenses to enforce or defend our rights.
In addition, we rely in part upon unpatented trade secrets, unpatented know-how, and continuing technological innovation which may not yet, or
may never be, patented, to develop and maintain our competitive position, which we seek to protect, in part, by confidentiality agreements with our
employees and consultants. We also have agreements with our employees and consultants that obligate them to assign their inventions to us. It is possible
that technology relevant to our business will be independently developed by a person that is not a party to such an agreement. In addition, if the employees
and consultants who are parties to these agreements breach or violate the terms of these agreements, we may not have adequate remedies for any such
breach or violation, and we could lose our trade secrets through such breaches or violations. To the extent that our commercial partners, collaborators,
employees and consultants use intellectual property owned by others in their work for us, disputes may arise as to the rights in related or resulting know-
how and inventions. Further, our trade secrets could otherwise become known or be independently discovered by our competitors, which would harm our
business.
We are reliant on the ability of AMF, as licensor of certain intellectual property contained in our products, and may be reliant on, future licensors
to maintain their intellectual property and protect their intellectual property
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against misappropriation, infringement or other violation. In some instances, we may not have primary control over AMF’s, or our other future licensors’,
patent prosecution activities. With respect to licensed patents that were issued to our licensors, or patents that may issue on patent applications, third parties
may challenge their validity, enforceability or scope, which may result in such patents being narrowed or invalidated. As a licensee, we are reliant on AMF
to defend any third-party claims or consent to our defending them on their behalf. Our licensors may not defend or prosecute such actions as vigorously or
in the manner that we would have if entitled to do so, and we will be subject to any judgment or settlement resulting from such actions and our business
could be adversely affected.
If we are unable to protect the confidentiality of our trade secrets, our business or competitive position could be harmed.
In addition to patent protection, we also rely upon other non-patent protection, such as: trademark, or, trade secret protection, as well as
confidentiality agreements with our employees, consultants, vendors, and third parties, to protect our confidential and proprietary information. Despite the
existence of such confidentiality agreements, or other contractual restrictions, we may not be able to prevent the unauthorized disclosure or use of our
confidential proprietary information or trade secrets by employees, consultants, vendors, and third parties. In addition to contractual measures, we try to
protect the confidential nature of our proprietary information using commonly accepted physical and technological security measures. Such measures may
not, for example, in the case of misappropriation of a trade secret by an employee or third party with authorized access, provide adequate protection for our
proprietary information. Our security measures may not prevent an employee or consultant from misappropriating our trade secrets and providing them to a
competitor, and, recourse we take against such misconduct may not provide an adequate remedy to fully protect our interests. Unauthorized parties may
also attempt to copy or reverse engineer certain aspects of our products that we consider proprietary. Enforcing a claim that a party illegally disclosed, or
misappropriated a trade secret, can be difficult, expensive and time-consuming, and, the outcome is unpredictable. Even though we use commonly accepted
security measures, trade secret violations are often a matter of state law, and the criteria for protection of trade secrets can vary among different
jurisdictions. Furthermore, the laws of foreign countries may not protect our trade secrets effectively or to the same extent as the laws of the United States.
In addition, trade secrets may be independently developed by others in a manner that could prevent legal recourse by us. If any of our confidential or
proprietary information, such as our trade secrets, were to be disclosed or misappropriated, or if any such information was independently developed by a
competitor, our business and competitive position could be harmed.
We may be unable to enforce our intellectual property rights throughout the world.
The laws of some foreign countries do not protect intellectual property rights to the same extent as the laws of the United States. Many companies
have encountered significant problems in protecting and defending intellectual property rights in certain foreign jurisdictions. If we face similar challenges
with respect to material intellectual property matters, this could make it difficult for us to stop infringement of our foreign patents or our other intellectual
property rights. For example, some foreign countries have compulsory licensing laws under which a patent owner must grant licenses to third parties. In
addition, some countries limit the enforceability of patents against third parties, including government agencies or government contractors. In these
countries, patents may provide limited or no benefit. Patent protection must ultimately be sought on a country-by-country basis, which is an expensive and
time-consuming process with uncertain outcomes. Accordingly, we may choose not to seek patent protection in certain countries, and we will not have the
benefit of patent protection in such countries.
Litigation may be necessary in the future to enforce our intellectual property rights or protect our trade secrets or other proprietary information,
which is an expensive and time-consuming process with uncertain outcomes. Proceedings to enforce our patent rights in foreign jurisdictions could result in
substantial costs and divert our efforts and attention from the commercialization of our products. Accordingly, our efforts to protect our intellectual
property rights in such countries may be inadequate. In addition, changes in the law and legal decisions by courts in the United States and foreign countries
may affect our ability to obtain adequate protection for our technology and the enforcement of our intellectual property.
Third parties may assert ownership or commercial rights to inventions we develop.
Third parties may, in the future, make claims challenging the inventorship or ownership of our intellectual property. In addition, we may face
claims by third parties that our agreements with employees, contractors or
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consultants obligating them to assign intellectual property to us are ineffective or in conflict with prior or competing contractual obligations of assignment,
which could result in ownership disputes regarding intellectual property we have developed or will develop and interfere with our ability to capture the
commercial value of such intellectual property. Litigation may be necessary to resolve an ownership dispute, and if we are not successful, we may be
precluded from using certain intellectual property or we may lose our rights in that intellectual property. Either outcome could harm our business and
competitive position.
We may be subject to claims that our employees, consultants or independent contractors have wrongfully used or disclosed confidential
information of third parties.
We employ individuals who previously worked with other companies, including our competitors or potential competitors. We may be subject to
claims that we or our employees, consultants or independent contractors have inadvertently or otherwise used or disclosed confidential information,
including trade secrets or other proprietary information, of former employers or other third parties. We may also be subject to claims that former employers
or other third parties have an ownership interest in our patents. Litigation may be necessary to defend against these claims. We may not be successful in
defending these claims, and even if we are successful, litigation could result in substantial cost and be a distraction to our management and other
employees. Any litigation or the threat thereof may adversely affect our ability to hire employees and we may lose valuable intellectual property rights if
we fail in defending any such claims. A loss of key personnel or their work product could diminish or prevent our ability to commercialize our products,
which could have an adverse effect on our business, results of operations and financial condition.
If we fail to comply with our obligations under our patent licenses with third parties, we could lose license rights that are important to our
business.
We are a party to the License Agreement with AMF and we may be a party to future license agreements. One or more of our licensors may allege
that we have breached our license agreement with them, and accordingly seek to terminate our license. If successful, this could result in our loss of the right
to use the licensed intellectual property, which could adversely affect our ability to commercialize our products, as well as harm our competitive business
position and our business prospects. In particular, the License Agreement imposes various development, royalty, insurance and other obligations on us. If
we fail to comply with these obligations or otherwise materially breach the License Agreement, AMF may have the right to terminate the License
Agreement, in which event we would not be able to market our products. In addition, any claims asserted against us by AMF may be costly and time-
consuming, divert the attention of key personnel from business operations or otherwise have a material adverse effect on our business.
Risks Related to Our Common Stock
The trading price of our common stock may be volatile, and purchasers of our common stock could incur substantial losses.
Our stock price may be volatile. The stock market in general and the market for medical technology companies in particular have experienced
extreme volatility that has often been unrelated to the operating performance of particular companies. The market price for our common stock may be
influenced by many factors, some of which are beyond our control, including:
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the impact of worldwide pandemics on voluntary surgical procedures;
unanticipated safety concerns related to the use of our products;
FDA or other U.S. or foreign regulatory or legal actions or changes affecting us or our industry;
intellectual property, product liability or other litigation against us, our third-party manufacturers or other parties on which we rely or
litigation against our general industry;
any termination or loss of rights under the License Agreement;
any voluntary or regulatory mandated product recalls;
adverse developments concerning our manufacturers or suppliers or any future strategic partnerships;
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introductions and announcements of new technologies by us, any commercialization partners or our competitors, and the timing of these
introductions and announcements;
announcements of regulatory approval or disapproval of our products or for any future enhancements to our products;
adverse results from or delays in clinical studies of our products;
our ability to successfully integrate acquired operations into our ongoing business;
variations in our financial results or those of companies that are perceived to be similar to us;
success or failure of competitive products or therapies in the SNM market;
changes in the structure of healthcare payment of our products;
announcements by us or our competitors of significant acquisitions, licenses, strategic partnerships, joint ventures or capital commitments;
• market conditions in the medical technology industry and issuance of securities analysts’ reports or recommendations;
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quarterly variations in our results of operations or those of our competitors;
changes in financial estimates or guidance, including our ability to meet our future revenue and operating profit or loss estimates or guidance;
the public’s reaction to our earnings releases, other public announcements and filings with the SEC;
rumors and market speculation involving us or other companies in our industry;
sales of substantial amounts of our stock by directors, officers or significant stockholders, or the expectation that such sales might occur;
general economic, industry and market conditions, including the size and growth, if any, of the market;
news reports relating to trends, concerns and other issues in the market or industry;
operating and stock performance of other companies that investors deem comparable to us and overall performance of the equity markets;
additions or departures of key personnel;
changes in our capital structure, such as future issuances of securities and the incurrence of additional debt;
changes in accounting standards, policies, guidelines, interpretations or principles;
the results of any future legal proceedings; and
other factors described in this “Risk Factors” section.
In addition, in the past, stockholders have initiated class action lawsuits against companies following periods of volatility in the market prices of
these companies’ common stock. Such litigation, if instituted against us, regardless of the merit or ultimate results of such litigation, could cause us to incur
substantial costs and divert management’s attention and resources.
We are obligated to develop and maintain proper and effective internal controls over financial reporting and any failure to maintain the
adequacy of these internal controls may adversely affect investor confidence in us, and, as a result, the value of our common stock.
To comply with the requirements of being a public company, we are required to maintain internal control over financial reporting and to report any
material weaknesses in such internal control. Section 404 of the Sarbanes-Oxley Act requires that we evaluate and determine the effectiveness of our
internal control over financial reporting and provide a management report on internal control over financial reporting. Further, the Sarbanes-Oxley Act also
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requires that our internal control over financial reporting be attested to by our independent registered public accounting firm.
If we have a material weakness in our internal control over financial reporting, we may not detect errors on a timely basis and our financial
statements may be materially misstated. The process of designing and implementing the internal control over financial reporting required to comply with
this obligation is time consuming, costly and complicated. If we identify material weaknesses in our internal control over financial reporting, if we are
unable to comply with the requirements of Section 404 in a timely manner, if we are unable to assert that our internal control over financial reporting are
effective, or if our independent registered public accounting firm is unable to express an opinion as to the effectiveness of our internal control over financial
reporting, investors may lose confidence in the accuracy and completeness of our financial reports and the market price of our common stock could be
adversely affected, and we could become subject to investigations by the stock exchange on which our securities are listed, the SEC, or other regulatory
authorities, which could require additional financial and management resources. In addition, if we are unable to continue to meet these requirements, we
may be unable to remain listed on Nasdaq.
Our disclosure controls and procedures may not prevent or detect all errors or acts of fraud.
We are continuing to refine our disclosure controls and procedures to provide reasonable assurance that information we must disclose in reports
we file or submit under the Exchange Act is accumulated and communicated to management, and recorded, processed, summarized and reported within the
time periods specified in the rules and forms of the SEC. We believe that any disclosure controls and procedures, no matter how well-conceived and
operated, can provide only reasonable, not absolute, assurance that the objectives of the control system are met.
These inherent limitations include the realities that judgments in decision-making can be faulty, and that breakdowns can occur because of simple
error or mistake. Additionally, controls can be circumvented by the individual acts of some persons, by collusion of two or more people or by an
unauthorized override of the controls. Accordingly, because of the inherent limitations in our control system, misstatements due to error or fraud may occur
and not be detected.
Our business could be negatively affected as a result of actions of activist stockholders, and such activism could impact the trading value of
our securities.
Stockholders may, from time to time, engage in proxy solicitations or advance stockholder proposals, or otherwise attempt to effect changes and
assert influence on our board of directors and management. Activist campaigns that contest or conflict with our strategic direction or seek changes in the
composition of our board of directors could have an adverse effect on our operating results and financial condition. A proxy contest would require us to
incur significant legal and advisory fees, proxy solicitation expenses and administrative and associated costs and require significant time and attention by
our board of directors and management, diverting their attention from the pursuit of our business strategy. Any perceived uncertainties as to our future
direction and control, our ability to execute on our strategy, or changes to the composition of our board of directors or senior management team arising
from a proxy contest could lead to the perception of a change in the direction of our business or instability which may result in the loss of potential business
opportunities, make it more difficult to pursue our strategic initiatives, or limit our ability to attract and retain qualified personnel and business partners, any
of which could adversely affect our business and operating results. If individuals are ultimately elected to our board of directors with a specific agenda, it
may adversely affect our ability to effectively implement our business strategy and create additional value for our stockholders. We may choose to initiate,
or may become subject to, litigation as a result of the proxy contest or matters arising from the proxy contest, which would serve as a further distraction to
our board of directors and management and would require us to incur significant additional costs. In addition, actions such as those described above could
cause significant fluctuations in our stock price based upon temporary or speculative market perceptions or other factors that do not necessarily reflect the
underlying fundamentals and prospects of our business.
Anti-takeover provisions in our certificate of incorporation and bylaws, as well as under Delaware law, could discourage a takeover.
Provisions in our certificate of incorporation and our bylaws may discourage, delay or prevent a merger, acquisition or other change in control of
us that stockholders may consider favorable, including transactions in
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which stockholders might otherwise receive a premium for their shares. These provisions could also limit the price that investors might be willing to pay in
the future for shares of our common stock, thereby depressing the market price of our common stock. In addition, these provisions may frustrate or prevent
any attempts by our stockholders to replace or remove our current management by making it more difficult for stockholders to replace or remove members
of our board of directors. Because our board of directors is responsible for appointing the members of our management team, these provisions could in turn
affect any attempt by our stockholders to replace or remove current members of our management team. These include the following provisions that:
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permit our board of directors to issue shares of preferred stock, with any rights, preferences and privileges as they may designate, without
stockholder approval, which could be used to dilute the ownership of a hostile bidder significantly;
provide that all vacancies, including newly created directorships, may, except as otherwise required by law, be filled by the affirmative vote of
a majority of directors then in office, even if less than a quorum;
require that any action to be taken by our stockholders must be effected at a duly called annual or special meeting of stockholders and not be
taken by written consent;
provide that stockholders seeking to present proposals before a meeting of stockholders or to nominate candidates for election as directors at a
meeting of stockholders must provide notice in writing in a timely manner and also specify requirements as to the form and content of a
stockholder’s notice, which may discourage or deter a potential acquiror from conducting a solicitation of proxies to elect the acquiror’s own
slate of directors or otherwise attempting to obtain control of our company;
prohibit cumulative voting in the election of directors, which limits the ability of minority stockholders to elect director candidates; and
provide that special meetings of our stockholders may be called only by the Chair of the board, our Chief Executive Officer or by our board of
directors pursuant to a resolution adopted by a majority of the total number of authorized directors, which may delay the ability of our
stockholders to force consideration by our company of a take-over proposal or to take certain corporate actions, including the removal of
directors.
In addition, Section 203 of the Delaware General Corporation Law (DGCL) which generally prohibits a Delaware corporation from engaging in
any of a broad range of business combinations with an interested stockholder who owns in excess of 15% of our outstanding voting stock from merging or
combining with us for a period of three years after the date of the transaction in which the person acquired in excess of 15% of our outstanding voting
stock, unless the merger or combination is approved in a prescribed manner. This provision could have the effect of delaying or preventing a change in
control of our company, whether or not it is desired by or beneficial to our stockholders. Further, other provisions of Delaware law may also discourage,
delay or prevent someone from acquiring us or merging with us.
Our certificate of incorporation designates the Court of Chancery of the State of Delaware as the sole and exclusive forum for certain types of
actions and proceedings that may be initiated by our stockholders, which could limit our stockholders’ ability to obtain a favorable judicial forum for
disputes with us or our directors, officers, employees or agents.
Our certificate of incorporation provides that, unless we consent in writing to an alternative forum, the Court of Chancery of the State of Delaware
will be the sole and exclusive forum for any derivative action or proceeding brought on our behalf, any action asserting a claim of breach of a fiduciary
duty owed by any of our directors, officers, employees or agents to us or our stockholders, any action asserting a claim arising pursuant to any provision of
the DGCL, our certificate of incorporation or our bylaws, any action asserting a claim that is governed by the internal affairs doctrine and the resolution of
any complaint asserting a cause of action arising under the Securities Act, in each case subject to the Court of Chancery having personal jurisdiction over
the indispensable parties named as defendants therein and the claim not being one which is vested in the exclusive jurisdiction of a court or forum other
than the Court of Chancery or for which the Court of Chancery does not have subject matter jurisdiction.
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Any person purchasing or otherwise acquiring any interest in any shares of our capital stock shall be deemed to have notice of and to have
consented to these provisions of our certificate of incorporation. These choice of forum provisions may limit our stockholders’ ability to bring a claim in a
judicial forum that they find favorable for disputes with us or our directors, officers, employees or agents, which may discourage such lawsuits against us
and our directors, officers, employees and agents even though an action, if successful, might benefit our stockholders. Stockholders who do bring a claim in
the Court of Chancery could face additional litigation costs in pursuing any such claim, particularly if they do not reside in or near Delaware. The Court of
Chancery may also reach different judgments or results than would other courts, including courts where a stockholder considering an action may be located
or would otherwise choose to bring the action, and such judgments or results may be more favorable to us than to our stockholders. Alternatively, if a court
were to find these provisions of our certificate of incorporation inapplicable to, or unenforceable in respect of, one or more of the specified types of actions
or proceedings, we may incur additional costs associated with resolving such matters in other jurisdictions, which could have a material adverse effect on
our business, financial condition or results of operations.
If securities or industry analysts do not publish research or publish inaccurate or unfavorable research about our business, our stock price
and trading volume could decline.
The trading market for our common stock will rely in part on the research and reports that securities or industry analysts publish about us and our
business. If one or more of the analysts who cover us downgrades our common stock or issues other unfavorable commentary or research the price of our
common stock may decline. If one or more analysts ceases coverage of our company or fails to publish reports on us regularly, demand for our stock could
decrease, which in turn could cause the trading price or trading volume of our common stock to decline and could result in the loss of all or part of your
investment in us.
We do not anticipate paying any cash dividends on our capital stock in the foreseeable future, so capital appreciation, if any, will be your sole
source of gain.
We have never declared or paid cash dividends on our capital stock. We currently intend to retain all of our future earnings, if any, to finance the
growth and development of our business. As a result, capital appreciation, if any, of our common stock will be your sole source of gain for the foreseeable
future.
Item 1B. Unresolved Staff Comments.
None.
Item 2. Properties.
In August 2014, we entered into a five-year operating lease for approximately 12,215 square feet of office space beginning on November 1, 2014,
and expiring on October 31, 2019. In June 2019, the lease was amended to extend the expiration date to October 31, 2020. In September 2020, the lease
was amended to extend the expiration date to July 31, 2022, and in December 2021, the lease was amended to extend the expiration date to January 31,
2028.
In November 2017, we entered into a seven-year operating lease for approximately 25,548 square feet of office space beginning on August 1,
2018, and expiring on August 31, 2025. In June 2019, the lease was amended to extend the expiration date to October 31, 2027. We have a renewal option
to extend the term of the lease for a period of five years beyond the initial term.
In June 2019, we entered into an eight-year operating lease for approximately 32,621 square feet of office space beginning on January 15, 2020 and
expiring on January 31, 2028. We use these premises as our new principal executive offices and for general office space. We are utilizing our other
currently-leased spaces to conduct the training of our sales team and for manufacturing purposes.
In August 2020, we entered into a 38-month operating lease for approximately 5,693 square feet of warehouse space beginning on October 15,
2020 and expiring on December 31, 2023. We use these premises for general warehouse space.
In March 2022, we entered into an 18-month operating lease for approximately 3,276 square feet of warehouse space beginning on July 1, 2022
and expiring on December 31, 2023. We use these premises for general warehouse space.
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For additional information, see Note 4 to the Consolidated Financial Statements in Part II, Item 8 of this Report.
Item 3. Legal Proceedings.
On November 4, 2019, Medtronic, Inc., Medtronic Puerto Rico Operations Co., Medtronic Logistics LLC and Medtronic USA, Inc. (collectively,
the Medtronic Affiliates) filed a complaint against us in the U.S. District Court for the Central District of California, Case No. 8:19-cv-2115, and amended
the complaint on November 26, 2019. We refer to this matter as the Medtronic Litigation. The complaint asserts that our rechargeable SNM system
infringes U.S. Patent Nos. 8,036,756, 8,626,314, 9,463,324 and 9,821,112 held by the Medtronic Affiliates, and the amended complaint further includes the
additional patents 8,738,148; 8,457,758; and 7,774,069 (collectively, the Medtronic Patents). The Medtronic Litigation requests customary remedies for
patent infringement, including (i) a judgment that we have infringed and are infringing the Medtronic Patents, (ii) damages, including treble damages for
willful infringement, (iii) a permanent injunction preventing us from infringing the Medtronic Patents, (iv) attorneys’ fees, and (v) costs and expenses. We
believe the allegations are without merit and are vigorously defending ourselves against them. We are unable to predict the likelihood of success of the
claims of the Medtronic Affiliates against us or to quantify any risk of loss. The Medtronic Litigation could last for an extended period of time and require
us to dedicate significant financial resources and management resources to our defense. An adverse ruling against us could materially and adversely affect
our business, financial position, results of operations or cash flows and could also result in reputational harm. Even if we are successful in defending
against these claims, the Medtronic Litigation could result in significant costs, delays in future product developments, reputational harm or other collateral
consequences. We are currently engaged in discovery in the Medtronic Litigation. A jury trial is scheduled in the Medtronic Litigation for April 2023.
In addition to the Medtronic Litigation, we are and may continue to be involved in claims, legal proceedings, and investigations arising out of our
operations in the normal course of business.
Item 4. Mine Safety Disclosures.
Not applicable.
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PART II
Item 5. Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity Securities.
Market for Common Stock
Our common stock has been publicly traded on the Nasdaq Global Select Market under the symbol “AXNX” since October 31, 2018. Prior to that date,
there was no public market for our common stock.
Holders of Record
At February 27, 2023, there were approximately 659 stockholders of record of our common stock. The actual number of stockholders is greater than this
number of record holders, and includes stockholders who are beneficial owners, but whose shares are held in street name by brokers and other nominees.
This number of holders of record also does not include stockholders whose shares may be held in trust by other entities.
Dividends
We have never declared or paid cash dividends on our common stock. Because we currently intend to retain all future earnings to finance future growth,
we do not anticipate paying any cash dividends in the near future.
Unregistered Sales of Equity Securities
Except as previously disclosed in our Quarterly Reports on Form 10-Q and Current Reports on Form 8-K, we had no sales of unregistered equity
securities during the year ended December 31, 2022.
Purchases of Equity Securities by the Issuer and Affiliated Purchasers
None.
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Performance Graph
The following graph illustrates a comparison of the total cumulative stockholder return on our common stock since October 31, 2018, which is the date
our common stock first began trading on the Nasdaq Global Select Market, to two indices: the Standard & Poor’s (S&P) 500 Stock Index and the S&P
Healthcare Equipment Index. The stockholder return shown in the graph below is not necessarily indicative of future performance, and we do not make or
endorse any predictions as to future stockholder returns. This graph shall not be deemed “soliciting material” or be deemed “filed” for purposes of
Section 18 of the Exchange Act, or otherwise subject to the liabilities under that Section, and shall not be deemed to be incorporated by reference into any
of our filings under the Securities Act, whether made before or after the date hereof and irrespective of any general incorporation language in any such
filing.
$100 investment in stock or index
Axonics, Inc. (AXNX)
S&P 500 Index (GSPC)
S&P 500 Health Care Equipment
Index (SPSIHE)
$
$
$
October 31,
2018
December 31,
2018
December 31,
2019
December 31,
2020
December 31,
2021
December 31,
2022
100.00 $
100.00 $
100.87 $
92.44 $
184.98 $
119.14 $
326.37 $
137.63 $
373.83 $
176.22 $
417.42
141.59
100.00 $
90.96 $
111.33 $
147.89 $
152.79 $
116.82
Item 6. [Reserved]
Not applicable.
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Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations.
Components of Our Results of Operations
Net Revenue
Revenue during the years ended December 31, 2022, 2021, and 2020 are as follows (in thousands):
SNM net revenue
United States
International markets
Bulkamid net revenue
United States
International markets
(1)
Total net revenue
_____________________________________________
Years Ended December 31,
2022
2021
2020
$
$
$
$
$
216,861 $
5,130
221,991 $
40,178 $
11,533
51,711 $
273,702 $
153,837 $
3,753
157,590 $
12,660 $
10,040
22,700 $
180,290 $
107,542
3,993
111,535
—
—
—
111,535
(1) The acquisition of Bulkamid was completed on February 25, 2021. Reported revenue includes sales from February 26, 2021 onwards.
Cost of Goods Sold and Gross Margin
Cost of goods sold consists primarily of costs of the components of our SNM systems, third-party contract labor costs, overhead costs, Bulkamid
product costs, as well as distribution-related expenses such as logistics and shipping costs. The overhead costs include the cost of material procurement and
operations supervision and management personnel. We expect overhead costs as a percentage of revenue to decrease as our sales volume increases. Cost of
goods sold also include other expenses such as scrap and inventory obsolescence. We expect cost of goods sold to increase in absolute dollars primarily as,
and to the extent, our revenue grows. We expect gross margin to vary based on manufacturing costs, regional differences in pricing, and discounts
negotiated by customers.
We calculate gross margin as gross profit divided by revenue. We expect future gross margin will be affected by a variety of factors, including
manufacturing costs, the average selling price of our products, the implementation of cost-reduction strategies, inventory obsolescence costs, which may
occur when new generations of our SNM systems are introduced, and to a lesser extent, the sales mix between the United States and international markets
as our average selling price in the United States is expected to be higher than in international markets and foreign currency exchange rates. Our gross
margin may increase over the long term to the extent our production volumes increase and we receive discounts on the costs charged by our contract
manufacturers, thereby reducing our per unit costs. Additionally, our gross margin may fluctuate from quarter to quarter as we continue to introduce new
products and adopt new manufacturing processes and technologies.
Research and Development Expenses
Research and development expenses consist primarily of employee compensation, including stock-based compensation, product development,
including testing and engineering, royalty expense, and clinical studies to develop and support our SNM systems, including clinical study and registry
management and monitoring, payments to clinical investigators, and data management. Other research and development expenses include consulting and
advisory fees, royalty expense, travel expenses, and equipment-related expenses and other miscellaneous office and facilities expenses related to research
and development programs. Research and development costs are expensed as incurred. We expect to continue incurring research and development expenses
in the future as we develop new products and expand to new markets. We expect research and development expenses as a percentage of revenue to vary
over time depending on the level and timing of initiating new product development efforts and new clinical development activities.
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The following table summarizes our research and development expenses by functional area for the years ended December 31, 2022, 2021, and
2020 (in thousands):
Personnel related
Clinical development
Contract R&D and manufacturing
Royalty expense
Other R&D expenses
Total R&D expenses
General and Administrative Expenses
Years Ended December 31,
2022
2021
2020
$
$
$
17,946
1,038
11,009
3,337
1,080
$
19,192
862
9,960
6,282
1,001
34,410 $
37,297 $
12,176
501
10,548
4,421
1,409
29,055
General and administrative expenses consist primarily of employee compensation, including stock-based compensation, and spending related to
finance, information technology, human resource functions, consulting, legal, and professional service fees. Other general and administrative expenses
include director and officer insurance premiums, investor relations costs, office-related expenses, facilities and equipment rentals, bad debt expense, travel
expenses, and impairment expenses. We expect our general and administrative expenses will significantly increase in absolute dollars as we increase our
headcount and expand administrative personnel to support our growth and operations as a public company including finance personnel and information
technology services. Additionally, we anticipate increased legal expenses associated with our patent infringement litigation with Medtronic. We expect
general and administrative expenses to decrease as a percentage of revenue primarily as, and to the extent, our revenue grows.
Sales and Marketing Expenses
Sales and marketing expenses consist primarily of employee compensation, including sales personnel commissions and stock-based compensation,
direct-to-consumer advertising programs, trade shows, booth exhibition costs, and the related travel for these events. Other sales and marketing expenses
include consulting, and advisory fees. We expect sales and marketing expenses to continue to increase in absolute dollars as we continue to expand our
commercial infrastructure to both drive and support our expected growth in revenue. However, we expect sales and marketing expenses to decrease as a
percentage of revenue in the long term primarily as, and to the extent, our revenue grows.
Amortization of Intangible Assets
Amortization of intangible assets consist primarily of amortization expense on patent license asset, manufacturing license asset, technology, and
customer relationships intangible assets. We amortize finite lived intangible assets over the period of estimated benefit using the straight-line method.
Acquisition-Related Costs
Acquisition-related costs consist of expenses incurred and changes in contingent consideration related to the Contura acquisition.
Other Income (Expense), Net
Other income (expense), net consists primarily of interest and accretion income earned on cash equivalents and short-term investments, gains and
losses on foreign currency transactions, net of interest expense payable under the Loan and Security Agreement with Silicon Valley Bank and other debt
arrangements.
Income Tax Expense (Benefit)
Income tax expense (benefit) primarily consists of losses benefited in certain foreign jurisdictions. We maintain a full valuation allowance for
deferred tax assets in our domestic operations, including net operating loss carryforwards and research and development credits.
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Results of Operations
Comparison of the Years Ended December 31, 2022 and 2021
The following table shows our results of operations for the years ended December 31, 2022 and 2021 (in thousands, except percentages):
Net revenue
Cost of goods sold
Gross profit
Gross Margin
Operating expenses
Research and development
General and administrative
Sales and marketing
Amortization of intangible assets
Acquisition-related costs
Total operating expenses
Loss from operations
Other income (expense)
Interest and other income
Loss on disposal of property and equipment
Interest and other expense
Other income (expense), net
Loss before income tax (benefit) expense
Income tax (benefit) expense
Net loss
Foreign currency translation adjustment
Comprehensive loss
Net Revenue
Years Ended December 31,
2022
2021
Period to Period
Change
$
273,702
76,037
197,665
72.2 %
$
180,290
64,572
115,718
64.2 %
34,410
40,238
156,019
9,383
22,561
262,611
(64,946)
5,133
(69)
(2,434)
2,630
(62,316)
(2,618)
(59,698)
(18,587)
(78,285)
$
37,297
30,041
105,789
7,241
7,158
187,526
(71,808)
40
(91)
(7,426)
(7,477)
(79,285)
782
(80,067)
(6,129)
(86,196)
$
93,412
11,465
81,947
(2,887)
10,197
50,230
2,142
15,403
75,085
6,862
5,093
22
4,992
10,107
16,969
(3,400)
20,369
(12,458)
7,911
$
$
Net revenue was $273.7 million in fiscal year 2022, an increase of $93.4 million, or 51.8%, compared to $180.3 million in fiscal year 2021. Net
revenues are primarily derived from the sale of our products to customers in the United States and certain international markets. The increase in net revenue
is due to increased sales of our products as we expanded our customer base in the U.S. and increased sales with our existing customer base. Our expanded
product offering of the recharge-free SNM system in March 2022 and the acquisition of the Bulkamid product in February 2021 have also contributed to
our expansion of customers and more patients being treated with our existing customers.
Cost of Goods Sold and Gross Margin
We incurred $76.0 million of cost of goods sold in fiscal year 2022. We incurred $64.6 million in fiscal year 2021. Gross margin was 72.2% in
fiscal year 2022, compared to 64.2% in fiscal year 2021. The increase in gross margin is primarily due to higher sales volumes and product mix, partially
offset by decreased inventory production and overhead absorption rates related to certain supply chain and labor constraints.
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Research and Development Expenses
Research and development expenses decreased $2.9 million, or 7.7%, to $34.4 million in fiscal year 2022, compared to $37.3 million in fiscal year
2021. The decrease in research and development expenses was primarily attributable to a decrease of $2.9 million in royalty expense due to lower net
revenue derived from the AMF Licensed Products and a decrease of $1.2 million in personnel costs including salaries and wages, stock-based
compensation and other employee-related benefits, partially offset by an increase of $1.0 million in contract R&D and manufacturing costs.
General and Administrative Expenses
General and administrative expenses increased $10.2 million, or 33.9%, to $40.2 million in fiscal year 2022, compared to $30.0 million in fiscal
year 2021, primarily as a result of an increase of $5.8 million in legal costs primarily related to the Medtronic Litigation, an increase of $1.5 million in
personnel costs including salaries and wages, stock-based compensation and other employee-related benefits, an increase of $1.1 million in facilities and
equipment costs, and an increase of $1.0 million in consulting and other professional service fees.
Sales and Marketing Expenses
Sales and marketing expenses increased $50.2 million, or 47.5%, to $156.0 million in fiscal year 2022, compared to $105.8 million in fiscal year
2021. The increase in sales and marketing expenses was primarily due to an increase of $32.8 million related to personnel costs including salaries, wages,
sales personnel commissions, stock-based compensation and other employee-related benefits primarily related to increased headcount and commissions
from the increase in net revenue, an increase of $12.8 million related to advertising expenses, and an increase of $4.0 million related to travel expenses.
Amortization of Intangible Assets
Amortization of intangible assets was $9.4 million in fiscal year 2022, compared to $7.2 million in fiscal year 2021. The increase in amortization
of intangible assets was primarily due to an increase of technology and customer relationships intangible assets acquired related to the Contura acquisition.
Acquisition-Related Costs
Acquisition-related costs were $22.6 million in fiscal year 2022 related to the change in fair value of contingent consideration. Acquisition-related
costs were $7.2 million in fiscal year 2021 related to the Contura acquisition and the change in fair value of contingent consideration.
Other Income (Expense), Net
Other income, net was $2.6 million in fiscal year 2022, consisting primarily of interest and other income earned on cash equivalents and short-
term investments, partially offset by losses on foreign currency transactions. Other expense, net was $7.5 million in fiscal year 2021, consisting primarily
of interest expense incurred related to the Loan Agreement with Silicon Valley Bank, partially offset by interest income earned on cash equivalents.
Income Tax (Benefit) Expense
Income tax benefit was $2.6 million in fiscal year 2022 primarily related to losses in certain foreign jurisdictions. Income tax expense was $0.8
million in fiscal year 2021 primarily related to the remeasurement of our U.K. deferred tax liabilities due to an increase in the U.K. income tax rate, net of
losses benefited in certain foreign jurisdictions.
Comparison of the Years Ended December 31, 2021 and 2020
For a comparison of our results of operations and cash flows for the years ended December 31, 2021 and 2020, see “Part II, Item 7. Management’s
Discussion and Analysis of Financial Condition and Results of Operations” of our annual report on Form 10-K for the year ended December 31, 2021 filed
with the SEC on March 1, 2022.
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Liquidity and Capital Resources
We only began full-scale commercialization of our rechargeable SNM system in late 2019. We have expended significant resources on research
and development activities, growing our operations organization and building and training our sales organization.
We incurred net losses of $59.7 million, $80.1 million, and $54.9 million for the years ended December 31, 2022, 2021, and 2020, respectively,
and had an accumulated deficit of $374.3 million as of December 31, 2022 compared to $314.6 million at December 31, 2021. We expect to continue to
spend a significant amount of our existing resources on sales and marketing activities as we continue to commercialize and market our products in the
United States and internationally.
As of December 31, 2022, we had cash, cash equivalents, and short-term investments of $357.2 million compared to $220.9 million at
December 31, 2021. We expect that our cash, cash equivalents, and short-term investments on hand will be sufficient to fund our operations through at least
the next 12 months. We fund our operations through a combination of proceeds from public offerings of our common stock and cash receipts from sales of
our products. As of December 31, 2022, we had no outstanding borrowings.
The following table sets out, as of December 31, 2022, our contractual obligations due by period (in thousands):
Operating Lease Obligations
Purchase Obligations
Other Long-Term Liabilities
(2)
(3)
(1)
Total
Total
Less than 1
year
$
$
10,897 $
63,772
2,200
76,869 $
2,162 $
63,772
200
66,134 $
1-3 years
3-5 years
More than 5
years
4,216 $
—
400
4,616 $
4,404 $
—
400
4,804 $
115
—
1,200
1,315
(1) Our principal office is currently located at 26 Technology Drive, Irvine, California 92618, where we lease approximately 25,548 square feet of office
space under a lease that terminates on October 31, 2027. In addition, we maintain offices at 15326 Alton Parkway, Irvine, California 92618, where
we lease approximately 32,621 square feet of office space under a lease that terminates on January 31, 2028, and at 7575 Irvine Center Drive,
Suite 200, Irvine, California 92618, where we lease approximately 12,215 square feet of space, and where we conduct the training of our sales
team, under a lease that terminates on January 31, 2028.
(2) Purchase obligations represent open purchase orders primarily for component materials and third-party contract labor costs at the end of the fiscal
year. These purchase orders can be impacted by various factors, including the timing of issuing orders, the timing of the shipment of orders, and
currency fluctuations.
(3) Represents the Minimum Royalty due under the License Agreement, and does not include royalty calculated as 4% of all net revenue derived from the
AMF Licensed Products.
From time to time we enter into certain types of contracts that contingently require us to indemnify parties against third-party claims, including the
License Agreement, and certain real estate leases, supply purchase agreements, and agreements with directors and officers. The terms of such obligations
vary by contract and in most instances a maximum dollar amount is not explicitly stated therein. Generally, amounts under these contracts cannot be
reasonably estimated until a specific claim is asserted, thus no liabilities have been recorded for these obligations on our balance sheets for any of the
periods presented.
Beyond the next 12 months, our cash requirements will depend primarily on the amount of continued cash receipts from sales of our products, as
well as our ability to develop or acquire new products, enter new markets, and compete effectively. We cannot accurately predict our long-term cash
requirements at this time. We may need to raise additional financing in the future to facilitate our business operations. If we raise additional funds by
issuing equity securities, our stockholders could experience dilution. Debt financing, if available, may involve covenants further restricting our operations
or our ability to incur additional debt. Any debt financing or additional equity that
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we raise may contain terms that are not favorable to us or our stockholders. Additional financing may not be available at all, or in amounts or on terms
acceptable to us. If we are unable to obtain additional financing when needed to satisfy our liquidity requirements, we may be required to scale back our
operations.
We do not have any off-balance sheet arrangements, as defined by applicable regulations of the SEC, that are reasonably likely to have a current or
future material effect on our financial condition, results of operations, liquidity, capital expenditures or capital resources.
Cash Flows
The following table presents a summary of our cash flow for the periods indicated (in thousands):
Net cash provided by (used in)
Operating activities
Investing activities
Financing activities
Effect of exchange rate changes on cash and cash equivalents
Net increase (decrease) in cash and cash equivalents
Net cash provided by (used in) operating activities
Years Ended December 31,
2022
2021
2020
$
$
3,191 $
(120,354)
133,968
1,163
17,968 $
(47,306) $
(143,002)
170,513
(508)
(20,303) $
(83,742)
9,654
144,190
(3)
70,099
Net cash provided by operating activities was $3.2 million in fiscal year 2022 and consisted primarily of non-cash charges of $65.8 million,
partially offset by a net loss of $59.7 million and a decrease from changes in net operating assets of $2.9 million. Net operating assets consisted primarily
of inventory and accounts receivable due to the commercial growth of our SNM systems in the United States and the addition of Bulkamid sales. Non-cash
charges consisted primarily of stock-based compensation and change in fair value of contingent consideration.
Net cash used in operating activities was $47.3 million in fiscal year 2021 and consisted primarily of a net loss of $80.1 million, a decrease from
changes in net operating assets of $9.8 million, partially offset by non-cash charges of $42.6 million. Net operating assets consisted primarily of inventory
and accounts receivable due to the commercial growth of our rechargeable SNM system in the United States and the addition of Bulkamid sales. Non-cash
charges consisted primarily of stock-based compensation and depreciation and amortization.
Net cash used in operating activities was $83.7 million in fiscal year 2020 and consisted primarily of a net loss of $54.9 million, a decrease from
changes in net operating assets of $47.0 million, partially offset by non-cash charges of $18.2 million. Net operating assets consisted primarily of inventory
to support the commercial launch of our rechargeable SNM system in the United States. Non-cash charges consisted primarily of stock-based
compensation.
Net cash (used in) provided by investing activities
Net cash used in investing activities was $120.4 million in fiscal year 2022 and consisted of purchases of short-term investments, partially offset
by sales and maturities of short-term investments.
Net cash used in investing activities was $143.0 million in fiscal year 2021 and consisted primarily of the $140.7 million paid for the acquisition
of Contura.
Net cash provided by investing activities was $9.7 million in fiscal year 2020 and consisted primarily of sales and maturities of short-term
investments, partially offset by purchases of property and equipment.
Net cash provided by financing activities
Net cash provided by financing activities was $134.0 million in fiscal year 2022 and consisted primarily of $128.3 million in net proceeds received
in the August 2022 follow-on offering and proceeds from exercise of stock options.
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Net cash provided by financing activities was $170.5 million in fiscal year 2021 and consisted primarily of $190.0 million in net proceeds received
in the May 2021 follow-on offering, partially offset by a net debt repayment of $26.1 million.
Net cash provided by financing activities was $144.2 million in fiscal year 2020 and consisted primarily of $140.5 million in net proceeds received
in the May 2020 follow-on offering.
Indebtedness
In June 2021, the principal amount, accrued interest, accrued loan fees, and prepayment fees related to the term loan under the Loan and Security
Agreement with Silicon Valley Bank entered into in February 2021 were paid in full. The unamortized debt issuance costs of $4.4 million were expensed
and recognized as interest expense.
In January 2021, the principal amount, accrued interest, accrued loan fees, and prepayment fees related to the Term Loan were paid in full. The
unamortized debt issuance costs of $0.4 million were expensed and recognized as interest expense.
We have no current indebtedness arrangements.
Critical Accounting Policies and Estimates
The preparation of consolidated financial statements in conformity with accounting principles generally accepted in the United States (GAAP)
requires our management to make estimates and judgments that affect the reported amounts of assets, liabilities, and expenses, and related disclosure of
contingent assets and liabilities. We base our estimates on historical experience and on various other assumptions that we believe to be reasonable under the
circumstances. The results of this evaluation then form the basis for making judgments about the carrying values of assets and liabilities that are not readily
apparent from other sources. Actual results may differ from these estimates, and such differences may be material to our consolidated financial statements.
Significant items subject to such estimates and assumptions include the useful lives of property and equipment and intangible assets, the valuation of
contingent consideration liability, and the valuation of stock-based compensation.
While our significant accounting policies are more fully described in Note 1 to the Consolidated Financial Statements in Part II, Item 8 of this
Annual Report on Form 10-K, we believe the following discussion addresses our most critical accounting policies, which are those that are most important
to the portrayal of our financial condition and results of operations and require our most difficult, subjective and complex judgments.
Revenue Recognition
Revenue recognized during the years ended December 31, 2022, 2021, and 2020 relates entirely to the sale of our products to our customers and
distributors.
We have revenue arrangements that consist of a single performance obligation. We recognize revenue at the point in time when it transfers control
of promised goods to its customers. Revenue is measured as the amount of consideration it expected to be received in exchange for transferring goods. The
amount of revenue that is recognized is based on the transaction price, which represents the invoiced amount and includes estimates of variable
consideration such as discounts, where applicable. We also sell to distributors and apply the same policies as our revenue arrangements with customers,
specifically that revenue is recognized at the point in time when we transfer control of promised goods to our distributors. We do not offer rights of return
or price protection. The amount of variable consideration included in the transaction price may be constrained and is included only to the extent that it is
probable that a significant reversal in the amount of the cumulative revenue recognized under the contract will not occur in a future period. Payment terms,
typically less than three months, do not include a significant financing component. We extend credit to our customers and distributors based upon an
evaluation of their financial condition and credit history and generally require no collateral. We do not have any contract balances related to product sales.
We also do not have significant contract acquisition costs related to product sales.
Shipping and handling costs incurred for the delivery of goods to customers and distributors are included in cost of goods sold. Amounts billed to
customers and distributors for shipping and handling are included in net revenue.
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Fair Value of Financial Instruments
Fair value is defined as the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market
participants at the measurement date. A three-level fair value hierarchy prioritizes the inputs used to measure fair value. The hierarchy requires entities to
maximize the use of observable inputs and minimize the use of unobservable inputs. The three levels of inputs used to measure fair value are as follows:
•
•
•
Level 1: Inputs are unadjusted quoted prices in active markets for identical assets or liabilities.
Level 2: Inputs are quoted prices for similar assets and liabilities in active markets or quoted prices for identical or similar instruments in markets
that are not active and model-derived valuations in which all significant inputs and significant value drivers are observable in active markets.
Level 3: Inputs are unobservable inputs based on our assumptions and valuation techniques used to measure assets and liabilities at fair value. The
inputs require significant management judgment or estimation.
Our assessment of the significance of an input to the fair value measurement requires judgment, which may affect the valuation of fair value assets
and liabilities and their placement within the fair value hierarchy levels. The carrying amounts reported in the consolidated financial statements
approximate the fair value for cash and cash equivalents, accounts receivable, and accounts payables, due to their short-term nature.
The purchase price of business acquisitions is primarily allocated to the tangible and identifiable intangible assets acquired and liabilities assumed
based on their estimated fair values on the acquisition date, with the excess recorded as goodwill.
Certain of our business combinations involve potential payment of future consideration that is contingent upon the achievement of certain product
development milestones and/or contingent on the acquired business reaching certain performance milestones. A liability is recorded for the estimated fair
value of the contingent consideration on the acquisition date. The fair value of the contingent consideration is remeasured at each reporting period, and the
change in fair value is recognized within operating expenses in the consolidated statements of comprehensive loss.
Contingent consideration represents contingent milestone, performance and revenue-sharing payment obligations related to acquisitions and is
measured at fair value, based on significant inputs not observable in the market, which represents a Level 3 measurement within the fair value hierarchy.
The valuation of contingent consideration is estimated using a binary option-based approach with assumptions we believe would be made by a market
participant. Significant inputs include projected revenues, discount rates, volatility factors and risk-free rates. We assess these assumptions on an ongoing
basis as additional data impacting the assumptions is obtained and any change in fair value of the contingent consideration is recorded within acquisition-
related costs in the consolidated statements of comprehensive loss. Significant increases or decreases in any of those inputs in isolation would result in a
significantly lower or higher fair value measurement. Generally, a change in the assumption used for the projected revenues would result in a directionally
similar change to the overall estimate of the contingent consideration.
Foreign Currency Translation
The functional currencies of the Company’s subsidiaries are currencies other than the U.S. dollar. The Company translates assets and liabilities of
the foreign subsidiaries into U.S. dollars at the exchange rate in effect on the balance sheet date. Revenue and expenses of the subsidiaries are translated
into U.S. dollars at the average exchange rate during the period. Gains or losses from these translation adjustments are reported as a separate component of
stockholders’ equity in accumulated other comprehensive gain or loss until there is a sale or complete or substantially complete liquidation of the
Company’s investment in the foreign subsidiary at which time the gains or losses will be realized and included in net income (loss).
Goodwill
Goodwill represents the excess purchase price over the fair values of both tangible and intangible assets acquired less the liabilities assumed.
Goodwill is tested for impairment at the reporting unit level by comparing the
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reporting unit’s carrying amount to the fair value of the reporting unit. The fair values are estimated using an income and discounted cash flow approach.
We evaluate our goodwill on an annual basis in the fourth quarter or more frequently if we believe indicators of impairment exist. We assess qualitative
factors to determine whether it is more likely than not that the fair value of a reporting unit is less than its carrying amount or perform an annual
impairment test. When tested quantitatively, we compare the fair value of the applicable reporting unit with its carrying value. In making this assessment,
management relies on a number of factors, including expected future operating results, business plans, economic projections, anticipated future cash flows,
business trends and declines in our market capitalization. We estimate the fair value of our reporting unit using a combination of the discounted cash flow
and income approaches. If the carrying amount of a reporting unit exceeds the reporting unit’s fair value, the amount by which the carrying value exceeds
the fair value is recognized as an impairment loss.
Impairment of Long-Lived Assets
We review our long-lived assets for impairment whenever events or changes in circumstances indicate that the carrying amount of an asset may
not be recoverable. Recoverability is measured by comparing the carrying amount to the future net cash flows that the assets are expected to generate. If
said assets are considered to be impaired, the impairment that would be recognized is measured by the amount by which the carrying amount of the assets
exceeds the projected discounted future net cash flows arising from the asset.
Indefinite-lived intangible assets are tested for impairment annually in the fourth quarter of the fiscal year and whenever events or changes in
circumstances indicate that the carrying amount may be impaired. Impairment is calculated as the excess of the asset’s carrying value over its fair value.
Fair value is generally determined using a discounted future cash flow analysis.
Research and Development
Research and development costs are charged to operations as incurred. Research and development costs include salary and personnel-related costs,
costs of clinical studies and testing, royalty expense, supplies and materials, and outside consultant costs.
Income Taxes
We account for income taxes using the asset and liability method to compute the difference between the tax basis of assets and liabilities and the
related financial amounts, using currently enacted tax rates. We have net deferred tax assets in certain jurisdictions. The realization of these deferred tax
assets is dependent upon our ability to generate sufficient taxable income in future years. Valuation allowances are established, when necessary, to reduce
deferred tax assets to the amount that more likely than not will be realized. We evaluate the recoverability of the deferred tax assets annually and maintain a
full valuation allowance on our U.S. net deferred tax assets. We recognize the tax benefit from an uncertain tax position only if it is more likely than not
that the tax position will be sustained on examination by taxing authorities, based on the technical merits of the position. We are subject to transfer pricing
and other tax regulations designed to ensure that appropriate levels of income are reported as earned by our U.S. and foreign entities and are taxed
accordingly. In the normal course of business, we are audited by federal, state and foreign tax authorities, and subject to inquiries from those tax authorities
regarding the amount of taxes due. These inquiries may relate to the timing and amount of deductions and the allocation of income among various tax
jurisdictions. Our policy is to recognize interest and penalties related to unrecognized tax benefits, if any, in income tax expense.
Stock-Based Compensation
We measure the cost of employee and non-employee services in exchange for an award of equity instruments based on the grant-date fair value of
the award and recognize compensation cost over the requisite service period (typically the vesting period), generally three or four years. Forfeitures are
estimated at the time of the grant and revised in subsequent periods to reflect differences between the estimates and the number of shares that actually
become exercisable. We use the Black-Scholes option pricing model to determine the fair value of stock options (as of the date of grant) that have service
conditions for vesting. Stock options and restricted shares awards vest based on service conditions, typically over three or four years.
We also grant shares of performance-based restricted stock units that typically vest after one year only if we have also achieved certain
performance objectives as defined and approved by our board of directors. The fair value
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of performance awards is determined based on the Company’s stock price at the date of grant and expensed over the performance period based on the
probability of achieving the performance objectives. If such targets are not met or service is not rendered for the requisite service period, no compensation
cost is recognized, and any recognized compensation cost in prior periods will be reversed. In addition, we also grant market-based restricted stock units
that have combined market conditions and service conditions for vesting, for which we use the Monte Carlo valuation model to value equity awards (as of
the date of grant). Compensation cost is not adjusted if the market condition is not met, as long as the requisite service is provided.
Recent Accounting Pronouncements
For recent accounting pronouncements, see Note 1, Nature of Operations and Summary of Significant Accounting Policies, of Notes to
Consolidated Financial Statements in Part II, Item 8 of this Annual Report.
Item 7A. Quantitative and Qualitative Disclosures About Market Risk.
We are exposed to market risks in the ordinary course of our business. These risks primarily include interest rate risk, foreign currency exchange
rate risk and inflation risk as follows:
Interest Rate Risk
We had cash, cash equivalents, and short-term investments of $357.2 million as of December 31, 2022, which came from public offerings of our
common stock and cash receipts from our product sales. The goals of our investment policy are liquidity and capital preservation and we do not enter into
investments for trading or speculative purposes. We believe that we do not have any material exposure to changes in the fair value of these assets as a result
of changes in interest rates due to the short term nature of our cash, cash equivalents, and short-term investments. A hypothetical 10% relative change in
interest rates during any of the periods presented would not have had a material impact on our consolidated financial statements. We do not currently
engage in hedging transactions to manage our exposure to interest rate risk.
Foreign Currency Exchange Rate Risk
As we expand internationally our results of operations and cash flows may become increasingly subject to fluctuations due to changes in foreign
currency exchange rates. All of our revenue is denominated in U.S. dollars. Our expenses are generally denominated in the currencies in which our
operations are located, which is primarily in the United States. The effect of a 10% adverse change in exchange rates on foreign denominated cash,
receivables and payables would not have been material for the periods presented. As our operations in countries outside of the United States grow, our
results of operations and cash flows may be subject to fluctuations due to changes in foreign currency exchange rates, which could harm our business in the
future. To date, we have not entered into any material foreign currency hedging contracts although we may do so in the future.
Inflation Risk
Inflationary factors, such as increases in our cost of goods sold and operating expenses, may adversely affect our operating results. Although we
do not believe that inflation has had a material impact on our financial position or results of operations to date, a high rate of inflation in the future may
have an adverse effect on our ability to maintain and increase our gross margin and operating expenses as a percentage of our revenue if the selling prices
of our products do not increase as much as or more than these increased costs.
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Item 8. Financial Statements and Supplementary Data.
Report of Independent Registered Public Accounting Firm
Shareholders and Board of Directors
Axonics, Inc.
Irvine, California
Opinion on the Consolidated Financial Statements
We have audited the accompanying consolidated balance sheets of Axonics, Inc. (the “Company”) as of December 31, 2022 and 2021, the related
consolidated statements of comprehensive loss, stockholders’ equity, and cash flows for each of the three years in the period ended December 31, 2022, and
the related notes (collectively referred to as the “consolidated financial statements”). In our opinion, the consolidated financial statements present fairly, in
all material respects, the financial position of the Company at December 31, 2022 and 2021, and the results of its operations and its cash flows for each of
the three years in the period ended December 31, 2022, in conformity with accounting principles generally accepted in the United States of America.
We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States) (“PCAOB”), the Company’s
internal control over financial reporting as of December 31, 2022, based on criteria established in Internal Control – Integrated Framework (2013) issued
by the Committee of Sponsoring Organizations of the Treadway Commission (“COSO”) and our report dated March 1, 2023 expressed an adverse opinion
thereon.
Basis for Opinion
These consolidated financial statements are the responsibility of the Company’s management. Our responsibility is to express an opinion on the Company’s
consolidated financial statements based on our audits. We are a public accounting firm registered with the PCAOB and are required to be independent with
respect to the Company in accordance with the U.S. federal securities laws and the applicable rules and regulations of the Securities and Exchange
Commission and the PCAOB.
We conducted our audits in accordance with the standards of the PCAOB. Those standards require that we plan and perform the audit to obtain reasonable
assurance about whether the consolidated financial statements are free of material misstatement, whether due to error or fraud.
Our audits included performing procedures to assess the risks of material misstatement of the consolidated financial statements, whether due to error or
fraud, and performing procedures that respond to those risks. Such procedures included examining, on a test basis, evidence regarding the amounts and
disclosures in the consolidated financial statements. Our audits also included evaluating the accounting principles used and significant estimates made by
management, as well as evaluating the overall presentation of the consolidated financial statements. We believe that our audits provide a reasonable basis
for our opinion.
Critical Audit Matter
The critical audit matter communicated below is a matter arising from the current period audit of the consolidated financial statements that was
communicated or required to be communicated to the audit committee and that: (i) relates to accounts or disclosures that are material to the consolidated
financial statements and (ii) involved our especially challenging, subjective, or complex judgments. The communication of the critical audit matter does not
alter in any way our opinion on the consolidated financial statements, taken as a whole, and we are not, by communicating the critical audit matter below,
providing a separate opinion on the critical audit matter or on the accounts or disclosures to which it relates.
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Valuation of contingent consideration
As described in Note 9 to the consolidated financial statements, the Company completed the acquisition of Contura Limited for the purchase price of
approximately $204.7 million during the year ended December 31, 2021. A portion of the consideration is contingent on future sales. The fair value of
contingent consideration increased from $10.4 million as of December 31, 2021 to $32.6 million as of December 31, 2022.
We identified the valuation of the contingent consideration related to the Contura Limited acquisition as a critical audit matter. The principal consideration
for our determination is the significant judgment used to develop the revenue growth rate in the forecast used in the valuation of the contingent
consideration. Auditing this consideration involved subjective auditor judgment due to the nature and extent of audit effort required to address these
matters, including the extent of specialized skill or knowledge needed.
The primary procedures we performed to address this critical audit matter included:
• Assessing the reasonableness of the revenue growth rates used in the forecasted revenue by comparing to historical performance, evaluating
operational metrics and considering contradictory evidence.
• Utilizing personnel with specialized knowledge and skill in valuation to assist in: (i) assessing the appropriateness of the valuation methodology;
and (ii) evaluating the potential effect of changes in the revenue growth rates on the fair value calculations.
/s/ BDO USA, LLP
We have served as the Company’s auditor since 2018.
Costa Mesa, California
March 1, 2023
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Axonics, Inc.
Consolidated Balance Sheets
(in thousands, except share and per share data)
December 31,
2022
2021
ASSETS
Current assets
Cash and cash equivalents
Short-term investments
Accounts receivable, net of allowance for credit losses of $321 and $355 at December 31, 2022 and 2021, respectively
Inventory, net
Prepaid expenses and other current assets
Total current assets
Property and equipment, net
Intangible assets, net
Other assets
Goodwill
Total assets
LIABILITIES AND STOCKHOLDERS’ EQUITY
Current liabilities
Accounts payable
Accrued liabilities
Accrued compensation and benefits
Operating lease liability, current portion
Other current liabilities
Total current liabilities
Operating lease liability, net of current portion
Deferred tax liabilities, net
Other long-term liabilities
Total liabilities
Commitments and contingencies (Note 4)
Stockholders’ equity
Preferred stock, par value $0.0001 per share; 10,000,000 shares authorized, no shares issued and outstanding at December 31, 2022
and 2021
Common stock, par value $0.0001 per share, 75,000,000 and 50,000,000 shares authorized at December 31, 2022 and 2021,
respectively; 49,546,727 and 46,330,167 shares issued and outstanding at December 31, 2022 and 2021, respectively
Additional paid-in capital
Accumulated deficit
Accumulated other comprehensive loss
Total stockholders’ equity
Total liabilities and stockholders’ equity
See accompanying notes to consolidated financial statements.
75
$
$
$
$
238,846 $
118,365
44,817
55,765
7,282
465,075
6,798
86,253
6,813
94,414
659,353 $
9,070 $
6,520
15,495
1,562
32,600
65,247
7,555
16,412
—
89,214
—
5
969,545
(374,264)
(25,147)
570,139
659,353 $
220,878
—
29,044
64,946
6,449
321,317
6,915
106,469
7,734
105,510
547,945
7,654
5,435
12,413
1,366
—
26,868
9,052
19,217
10,370
65,507
—
5
803,559
(314,566)
(6,560)
482,438
547,945
Table of Contents
Net revenue
Cost of goods sold
Gross profit
Operating expenses
Research and development
General and administrative
Sales and marketing
Amortization of intangible assets
Acquisition-related costs
Total operating expenses
Loss from operations
Other income (expense)
Interest and other income
Loss on disposal of property and equipment
Interest and other expense
Other income (expense), net
Loss before income tax (benefit) expense
Income tax (benefit) expense
Net loss
Foreign currency translation adjustment
Comprehensive loss
Axonics, Inc.
Consolidated Statements of Comprehensive Loss
(in thousands, except share and per share data)
2022
$
Years Ended December 31,
2021
2020
273,702 $
76,037
197,665
180,290 $
64,572
115,718
34,410
40,238
156,019
9,383
22,561
262,611
(64,946)
5,133
(69)
(2,434)
2,630
(62,316)
(2,618)
(59,698)
(18,587)
(78,285) $
37,297
30,041
105,789
7,241
7,158
187,526
(71,808)
40
(91)
(7,426)
(7,477)
(79,285)
782
(80,067)
(6,129)
(86,196) $
111,535
44,444
67,091
29,055
25,551
66,130
115
—
120,851
(53,760)
761
(41)
(1,874)
(1,154)
(54,914)
1
(54,915)
(3)
(54,918)
$
$
See accompanying notes to consolidated financial statements.
76
Net loss per share, basic and diluted (see Note 1)
Weighted-average shares used to compute basic and diluted net loss per share (see Note 1)
(1.28) $
(1.86) $
46,684,478
43,072,298
(1.48)
36,981,335
Table of Contents
Axonics, Inc.
Consolidated Statements of Stockholders’ Equity
(in thousands, except share and per share data)
Common Stock
Shares
34,110,995 $
Amount
Additional
Paid-in
Capital
Accumulated
Deficit
Accumulated
Other
Comprehensive
Loss
3 $
363,012 $
(179,584) $
(428) $
Balance at December 31, 2019
Issuance of common stock for employee stock option exercises
for cash
Restricted Shares Award (RSA) issuances and forfeitures for
terminations, net and stock-based compensation
Issuance of common stock for vesting of Restricted Stock Units
(RSU) and stock-based compensation
Follow-on offering - issuance of 4,600,000 shares at $32.50 per
share, less offering costs of $9,013
Foreign currency translation adjustment
Net loss
Balance at December 31, 2020
Issuance of common stock for employee stock option exercises
for cash
RSA issuances and forfeitures for terminations, net and stock-
based compensation
Issuance of common stock for vesting of RSU and stock-based
compensation
Follow-on offering - issuance of 4,025,000 shares at $50.00 per
share, less offering costs of $11,272
Issuance of common stock for acquisition of Contura Limited
Issuance of common stock for exclusive license asset
Foreign currency translation adjustment
Net loss
Balance at December 31, 2021
Issuance of common stock for employee stock option exercises
for cash
RSA issuances and forfeitures for terminations, net and stock-
based compensation
Issuance of common stock for vesting of RSU and stock-based
compensation
Follow-on offering - issuance of 2,012,500 shares at $63.85 per
share, less offering costs of $192
Foreign currency translation adjustment
Net loss
767,792
405,907
46,336
4,600,000
—
—
39,931,030
522,495
520,411
169,054
4,025,000
1,096,583
65,594
—
—
46,330,167
364,352
570,778
268,930
2,012,500
—
—
—
—
—
1
—
—
4
—
—
—
1
—
—
—
—
5
—
—
—
—
—
—
Balance at December 31, 2022
49,546,727 $
5 $
3,703
11,792
3,303
140,486
—
—
522,296
6,757
17,793
7,371
189,977
55,728
3,637
—
—
803,559
5,662
26,218
5,800
—
—
—
—
—
(54,915)
(234,499)
—
—
—
—
—
—
—
(80,067)
(314,566)
—
—
—
—
—
—
—
(3)
—
(431)
—
—
—
—
—
—
(6,129)
—
(6,560)
—
—
—
128,306
—
—
969,545 $
—
—
(59,698)
(374,264) $
—
(18,587)
—
(25,147) $
Total
183,003
3,703
11,792
3,303
140,487
(3)
(54,915)
287,370
6,757
17,793
7,371
189,978
55,728
3,637
(6,129)
(80,067)
482,438
5,662
26,218
5,800
128,306
(18,587)
(59,698)
570,139
See accompanying notes to consolidated financial statements.
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Table of Contents
Axonics, Inc.
Consolidated Statements of Cash Flows
(in thousands)
Cash Flows from Operating Activities
Net loss
Adjustments to reconcile net loss to net cash provided by (used in) operating activities
Depreciation and amortization
Loss on disposal of property and equipment
Stock-based compensation
Amortization of debt issuance costs
(Reversal of) provision for allowance of credit losses
Change in fair value of contingent consideration
Deferred income taxes and other items, net
Changes in operating assets and liabilities, net of business acquisition
Accounts receivable
Inventory
Prepaid expenses and other current assets
Other assets
Accounts payable
Accrued liabilities
Accrued compensation and benefits
Lease liability
Net cash provided by (used in) operating activities
Cash Flows from Investing Activities
Purchases of property and equipment
Acquisition of a business, net of cash acquired
Purchases of short-term investments
Proceeds from sales and maturities of short-term investments
Net cash (used in) provided by investing activities
Cash Flows from Financing Activities
Payment of debt issuance costs
Proceeds from debt
Repayment of debt
Proceeds from offering of common stock upon follow-on public offering
Payment of common stock offering costs upon follow-on public offering
Proceeds from exercise of stock options
Net cash provided by financing activities
Effect of exchange rate changes on cash and cash equivalents
Net increase (decrease) in cash and cash equivalents
Cash and cash equivalents, beginning of year
Cash and cash equivalents, end of year
Supplemental Disclosure of Cash Flow Information
Cash paid for interest
Cash paid for taxes
Noncash Investing and Financing Activities
Property and equipment acquired but not yet paid
Common stock issuance for business acquisition
Contingent consideration for business acquisition
Common stock issuance for exclusive license asset
Accrued loan fees as debt issuance costs
2022
Years Ended December 31,
2021
2020
$
(59,698) $
(80,067) $
(54,915)
11,721
69
32,018
—
(34)
22,230
(184)
(15,968)
8,423
(862)
(207)
1,468
1,032
3,112
71
3,191
(2,223)
—
(175,110)
56,979
(120,354)
—
—
—
128,498
(192)
5,662
133,968
1,163
17,968
220,878
238,846 $
1 $
667 $
67 $
— $
— $
— $
— $
9,126
91
25,164
4,991
(122)
2,740
582
(8,998)
(1,108)
(940)
(225)
(2,862)
(1,976)
6,155
143
(47,306)
(2,261)
(140,741)
—
—
(143,002)
(106)
75,000
(101,116)
201,250
(11,272)
6,757
170,513
(508)
(20,303)
241,181
220,878 $
2,178 $
1 $
— $
55,728 $
7,630 $
3,637 $
4,500 $
$
$
$
$
$
$
$
$
1,741
41
15,095
774
390
—
165
(10,781)
(47,353)
(863)
(90)
4,778
4,193
2,573
510
(83,742)
(2,938)
—
—
12,592
9,654
—
—
—
149,500
(9,013)
3,703
144,190
(3)
70,099
171,082
241,181
1,102
1
—
—
—
—
—
See accompanying notes to consolidated financial statements.
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AXONICS, INC.
NOTES TO CONSOLIDATED FINANCIAL STATEMENTS
Note 1. Nature of Operations and Summary of Significant Accounting Policies
Nature of Operations
Axonics, Inc. (the Company) was incorporated in the state of Delaware on March 2, 2012 under the name American Restorative Medicine, Inc.
The Company had no operations until October 1, 2013, when the license agreement between Alfred E. Mann Foundation for Scientific Research (AMF)
and the Company (the License Agreement) was entered into. In August 2013, the Company changed its name to Axonics Modulation Technologies, Inc. In
March 2021, the Company changed its name to Axonics, Inc.
The Company is a medical technology company that develops and commercializes innovative and minimally invasive products to treat bladder
and bowel dysfunction. The Company has designed and developed both rechargeable (R20™) and recharge-free (F15™) implantable sacral
neuromodulation (SNM) systems, which deliver mild electrical pulses to the targeted sacral nerve in order to restore normal communication to and from the
brain to reduce the symptoms of overactive bladder (OAB), urinary retention (UR) and fecal incontinence (FI). The Company’s products are protected by
intellectual property based on Company-generated innovations and patents and other intellectual property licensed from AMF. The Company has marketing
approvals in the United States, Europe, Canada, and Australia for all relevant clinical indications. The premarket approval (PMA) application for the
rechargeable SNM system for the treatment of FI was approved by the U.S. Food and Drug Administration (FDA) on September 6, 2019, and the PMA
application for the rechargeable SNM system for the treatment of OAB and UR was approved by the FDA on November 13, 2019. Accordingly, the
Company began U.S. commercialization of its rechargeable SNM system in the fourth quarter of 2019. Prior to the fourth quarter of 2019, the Company
derived revenue only from its international operations in select markets including England, the Netherlands and Canada, and its activities had consisted
primarily of developing the rechargeable SNM system, conducting its RELAX-OAB post-market clinical follow-up study in Europe, its ARTISAN-SNM
pivotal clinical study in the United States and hiring and training its U.S. commercial team in preparation for the launch of the rechargeable SNM system in
the United States.
Beginning in February 2021 with the acquisition of Contura Limited, the Company also markets Bulkamid®, a urethral bulking agent to treat
female stress urinary incontinence (SUI). Beginning in March 2022 with the FDA approval of the Company’s long-lived, recharge-free F15 SNM
implantable stimulator, the Company now markets and sells the F15 recharge-free system to customers in the United States in addition to the rechargeable
SNM system. The new recharge-free SNM system and Bulkamid are protected by intellectual property based on Company-generated innovations or patents
acquired as part of the Contura acquisition. For more information, see Note 9.
May 2020 Follow-On Offering
On May 12, 2020, the Company completed a follow-on offering by issuing 4,600,000 shares of common stock, at an offering price of $32.50 per
share, inclusive of 600,000 shares of the Company’s common stock issued upon the exercise by the underwriters of their option to purchase additional
shares. The net proceeds to the Company were approximately $140.5 million, after deducting underwriting discounts, commissions and offering expenses
payable by the Company.
May 2021 Follow-On Offering
On May 14, 2021, the Company completed a follow-on offering by issuing 4,025,000 shares of common stock, at an offering price of $50.00 per
share, inclusive of 525,000 shares of the Company’s common stock issued upon the exercise by the underwriters of their option to purchase additional
shares. The net proceeds to the Company were approximately $190.0 million, after deducting underwriting discounts, commissions and offering expenses
payable by the Company.
August 2022 Follow-On Offering
On August 5, 2022, the Company completed a follow-on offering by issuing 2,012,500 shares of common stock, at an offering price of $63.85 per
share, inclusive of 262,500 shares of the Company’s common stock issued
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upon the exercise by the underwriters of their option to purchase additional shares. The net proceeds to the Company were approximately $128.3 million,
after deducting offering expenses payable by the Company.
Principles of Consolidation
The accompanying consolidated financial statements include the accounts of the Company; its wholly-owned subsidiaries: Axonics Europe,
S.A.S., Axonics Modulation Technologies U.K. Limited, Axonics Modulation Technologies Australia Pty Ltd, Axonics Women’s Health Limited,
Bulkamid SARL, Axonics GmbH, and Contura, Inc. Intercompany accounts and transactions have been eliminated in consolidation.
Basis of Presentation
The accompanying consolidated financial statements have been prepared in accordance with accounting principles generally accepted in the
United States (GAAP). Certain prior year reported amounts have been reclassified to conform with the 2022 presentation.
COVID-19
The ongoing COVID-19 outbreak, and the resulting restrictions intended to slow the spread of COVID-19, including stay-at-home orders,
business shutdowns and other restrictions, has adversely affected the Company’s business in several ways. The primary impact on the Company’s business
was the cancellation or delay of elective procedures in certain areas to allow health care facilities to prioritize the treatment of COVID-19 patients during
the initial stages and resurgence periods of the pandemic or because patients are avoiding health care facilities that they feel are unsafe. These
developments materially reduced the number of procedures using the Company’s rechargeable SNM system. If governmental authorities recommend again
in the future that it is deemed advisable for health care facilities to not perform outpatient elective procedures, as was the case at various times throughout
2020 through 2022, the Company expects it would materially harm the Company’s revenues and potentially increase the Company’s operating loss. Even
as efforts to contain the pandemic have made progress and some restrictions have relaxed, new variants of the virus may continue to cause additional
outbreaks. These challenges will likely continue for the duration of the pandemic and could reduce the Company’s revenue and negatively impact the
Company’s business, financial condition and results of operations while the pandemic continues. If these delays in procedures occur in the future, the
Company may have to scale back its business, including reducing headcount, which could have a negative impact on the Company’s long-term operations.
The Company could also experience other negative impacts of the COVID-19 outbreak such as the lack of availability of the Company’s key personnel,
temporary closures of the Company’s office or the facilities of the Company’s business partners, customers, third party service providers or other vendors,
and the interruption of the Company’s supply chain, distribution channels, liquidity and capital or financial markets.
Any disruption and volatility in the global capital markets as a result of the pandemic may increase the Company’s cost of capital and adversely
affect the Company’s ability to access financing when and on terms that the Company desires. In addition, a recession resulting from the spread of COVID-
19 could materially affect the Company’s business, especially if a recession results in higher unemployment causing potential patients to not have access to
health insurance.
The ultimate extent to which the COVID-19 pandemic and its repercussions impact the Company’s business will depend on future developments,
which are highly uncertain. However, the foregoing and other continued disruptions to the Company’s business as a result of COVID-19 could result in a
material adverse effect on the Company’s business, results of operations, financial condition and cash flows.
Use of Estimates
The preparation of consolidated financial statements in conformity with GAAP requires the Company’s management to make estimates and
judgments that affect the reported amounts of assets, liabilities, and expenses, and related disclosure of contingent assets and liabilities. The Company
bases its estimates on historical experience and on various other assumptions that it believes to be reasonable under the circumstances. The results of this
evaluation then form the basis for making judgments about the carrying values of assets and liabilities that are not readily apparent from other sources.
Actual results may differ from these estimates and such differences may be material to the consolidated financial statements. Significant items subject to
such estimates and assumptions include the useful lives of property and equipment and intangible assets, the valuation of deferred income tax assets and
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liabilities, the valuation of contingent consideration liability, the valuation of stock-based compensation, the product returns reserve, the inventory
obsolescence reserve and accounts receivable allowance for credit losses.
Revenue Recognition
Revenue recognized during the years ended December 31, 2022, 2021, and 2020 relates entirely to the sale of the Company’s products to its
customers and distributors.
The Company has revenue arrangements that consist of a single performance obligation. The Company recognizes revenue at the point in time
when it transfers control of promised goods to its customers. Revenue is measured as the amount of consideration it expected to be received in exchange for
transferring goods. The amount of revenue that is recognized is based on the transaction price, which represents the invoiced amount and includes estimates
of variable consideration such as discounts, where applicable. The Company also sells to distributors and applies the same policies as its revenue
arrangements with customers, specifically that revenue is recognized at the point in time when it transfers control of promised goods to its distributors. The
Company does not offer rights of return or price protection. The amount of variable consideration included in the transaction price may be constrained and
is included only to the extent that it is probable that a significant reversal in the amount of the cumulative revenue recognized under the contract will not
occur in a future period. Payment terms, typically less than three months, do not include a significant financing component. The Company extends credit to
its customers and distributors based upon an evaluation of their financial condition and credit history and generally requires no collateral. The Company
does not have any contract balances related to product sales. The Company also does not have significant contract acquisition costs related to product sales.
In accordance with Company policy and based on the Company’s historical experience, the allowance for product returns was $0.2 million and
$0.2 million at December 31, 2022 and 2021, respectively, and is recorded as a reduction of gross revenue in its consolidated statements of comprehensive
loss. Damaged or defective products are replaced at no charge under the Company’s standard warranty. For the years ended December 31, 2022, 2021, and
2020, the replacement costs were $0.2 million, $0.2 million, and $0.1 million, respectively. The replacement costs are recorded within the sales and
marketing expenses in its consolidated statements of comprehensive loss.
The Company offers its standard warranty to all customers. The Company does not sell any warranties on a standalone basis. The Company’s
warranty provides that its products are free of material defects and conform to specifications, and includes an offer to repair, replace or refund the purchase
price of defective products. This assurance does not constitute a service and is not considered a separate performance obligation. The Company estimates
warranty liabilities at the time of revenue recognition and records it as a charge to sales and marketing expense. The warranty liability as of December 31,
2022 and 2021 was $0.1 million and $0.1 million, respectively.
Shipping and handling costs incurred for the delivery of goods to customers and distributors are included in cost of goods sold. Amounts billed to
customers and distributors for shipping and handling are included in net revenue.
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The following table provides additional information pertaining to net revenue disaggregated by product and geographic market for the years ended
December 31, 2022, 2021, and 2020 (in thousands):
SNM net revenue
United States
International markets
Bulkamid net revenue
United States
International markets
(1)
Total net revenue
_____________________________________________
2022
Years Ended December 31,
2021
2020
$
$
$
$
$
216,861 $
5,130
221,991 $
40,178 $
11,533
51,711 $
273,702 $
153,837 $
3,753
157,590 $
12,660 $
10,040
22,700 $
180,290 $
107,542
3,993
111,535
—
—
—
111,535
(1) The acquisition of Bulkamid was completed on February 25, 2021. Reported revenue includes sales from February 26, 2021 onwards.
Allowance for Credit Losses
The Company makes estimates of the collectability of accounts receivable in accordance with ASU 2016-13, “Financial Instruments—Credit
Losses (Topic 326): Measurement of Credit Losses on Financial Instruments.” The Company’s estimate of future credit losses is made by management
based upon historical bad debts, customer receivable balances, age of customer receivable balances, customers’ financial conditions and reasonable
forecasted economic trends. Despite the Company’s efforts to minimize credit risk exposure, customers could be adversely affected if future economic and
industry trends, including those related to COVID-19, change in such a manner as to negatively impact their cash flows. The full effects of COVID-19 on
the Company’s customers are highly uncertain and cannot be predicted. As a result, the Company’s future collection experience can differ significantly
from historical collection trends. If the Company’s customers experience a negative impact on their cash flows, it could have a material adverse effect on
the Company’s results of operations and financial condition.
The following table summarizes the changes in our allowance for credit losses (in thousands):
Balance at beginning of period
Write-offs
Bad debt expense (recoveries)
Balance at end of period
Cash and Cash Equivalents
2022
Years Ended December 31,
2021
2020
$
$
355 $
(75)
41
321 $
465 $
(12)
(98)
355 $
75
—
390
465
Cash equivalents consist of short-term, highly liquid investments purchased with an original maturity of three months or less. Financial
instruments that potentially subject the Company to a concentration of credit risk consist of cash and cash equivalents. At times, the cash and cash
equivalent balances may exceed federally insured limits. The Company does not believe that this results in any significant credit risk as the Company’s
policy is to place its cash and cash equivalents in highly-rated financial institutions. The Company also holds cash in foreign banks that are not federally
insured. The Company has not experienced any losses on its deposits of cash and cash equivalents.
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Fair Value of Financial Instruments
Fair value is defined as the price that would be received to sell an asset or paid to transfer a liability in an orderly transaction between market
participants at the measurement date. A three-level fair value hierarchy prioritizes the inputs used to measure fair value. The hierarchy requires entities to
maximize the use of observable inputs and minimize the use of unobservable inputs. The three levels of inputs used to measure fair value are as follows:
•
•
•
Level 1: Inputs are unadjusted quoted prices in active markets for identical assets or liabilities.
Level 2: Inputs are quoted prices for similar assets and liabilities in active markets or quoted prices for identical or similar instruments in markets
that are not active and model-derived valuations in which all significant inputs and significant value drivers are observable in active markets.
Level 3: Inputs are unobservable inputs based on the Company’s assumptions and valuation techniques used to measure assets and liabilities at fair
value. The inputs require significant management judgment or estimation.
Level 1 investments include U.S. government and agency securities, which are valued based on prices readily available in the active markets in
which those securities are traded. Level 2 investments include commercial paper and corporate notes, which is valued on a recurring basis based on inputs
that are readily available in public markets or can be derived from information available in publicly quoted markets.
The Company’s assessment of the significance of an input to the fair value measurement requires judgment, which may affect the valuation of fair
value assets and liabilities and their placement within the fair value hierarchy levels. The carrying amounts reported in the consolidated financial statements
approximate the fair value for cash and cash equivalents, accounts receivable, and accounts payables, due to their short-term nature.
The purchase price of business acquisitions is primarily allocated to the tangible and identifiable intangible assets acquired and liabilities assumed
based on their estimated fair values on the acquisition date, with the excess recorded as goodwill.
Certain of the Company’s business combinations involve potential payment of future consideration that is contingent upon the achievement of
certain product development milestones and/or contingent on the acquired business reaching certain performance milestones. A liability is recorded for the
estimated fair value of the contingent consideration on the acquisition date. The fair value of the contingent consideration is remeasured at each reporting
period, and the change in fair value is recognized within operating expenses in the consolidated statements of comprehensive loss.
On February 25, 2021, the Company acquired Contura Limited and its Bulkamid product, a urethral bulking agent indicated for the treatment of
female SUI. In consideration for the acquisition, the Company paid approximately $141.3 million in cash and issued 1,096,583 shares of our common
stock. The Company may pay an additional $35 million in the event Bulkamid sales in any consecutive 12-month period exceed $50 million (the
Milestone) before December 31, 2024, with payment due within 50 business days following the quarter in which the Milestone has been met.
Contingent consideration represents contingent milestone, performance and revenue-sharing payment obligations related to acquisitions and is
measured at fair value, based on significant inputs not observable in the market, which represents a Level 3 measurement within the fair value hierarchy.
The valuation of contingent consideration is estimated using a binary option-based approach with assumptions the Company believes would be made by a
market participant. Significant inputs include projected revenues, discount rates, volatility factors and risk-free rates. The Company assesses these
assumptions on an ongoing basis as additional data impacting the assumptions is obtained and any change in fair value of the contingent consideration is
recorded within acquisition-related costs in the consolidated statements of comprehensive loss. Significant increases or decreases in any of those inputs in
isolation would result in a significantly lower or higher fair value measurement. Generally, a change in the assumption used for the projected revenues
would result in a directionally similar change to the overall estimate of the contingent consideration. At December 31, 2022, the discount rates ranged from
8.5% to 9.0%, volatility was estimated at 24.5%, and risk-free rates ranged from 4.3% to 4.8%. The fair value of contingent consideration of $32.6 million
at December 31, 2022, is reflected in other current liabilities on the Company’s consolidated balance
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sheets, as the Milestone is expected to be met within the next 12 months. The fair value of contingent consideration of $10.4 million at December 31, 2021,
is reflected in other long-term liabilities on the Company’s consolidated balance sheets.
The following table summarizes the changes in the fair value of recurring Level 3 fair value measurements during the years ended December 31,
2022 and 2021 (in thousands):
Liabilities
Contingent consideration:
December 31, 2020
February 25, 2021 Acquisition
Change in fair value included in earnings
December 31, 2021
Change in fair value included in earnings
December 31, 2022
$
$
—
7,630
2,740
10,370
22,230
32,600
There were no transfers between Levels 1, 2 or 3 for the periods presented.
Investment Securities
The Company classifies its investment securities as available-for-sale. Those investments in debt securities with maturities less than 12 months at
the balance sheet date are considered short-term investments. Those investments in debt securities with maturities greater than 12 months at the balance
sheet date are considered long-term investments. The Company’s investment securities classified as available-for-sale are recorded at fair value based on
the fair value hierarchy (Level 1 and Level 2 inputs in the fair value hierarchy), and consists primarily of commercial paper, corporate notes and U.S.
government and agency securities. Unrealized gains or losses, deemed temporary in nature, are reported as other comprehensive income (loss) within the
consolidated statements of comprehensive loss. There were no unrealized gains or losses during the years ended December 31, 2022, 2021, and 2020.
A decline in the fair value of any security below cost that is deemed other than temporary results in a charge to net income (loss) and the
corresponding establishment of a credit loss allowance for the security. Premiums (discounts) are amortized (accreted) over the life of the related security
as an adjustment to yield using the straight-line interest method. Dividend, accretion and interest income are recognized when earned. Realized gains or
losses are included in net loss and are derived using the specific identification method for determining the cost of securities sold.
The Company had no outstanding investment securities as of December 31, 2021. The following table presents the fair value hierarchy for those
assets measured at fair value on a recurring basis as of December 31, 2022 (in thousands):
(1)
Assets :
Commercial paper
Corporate notes
U.S. government and agency securities
_____________________________________________
Fair Value Measurements at December 31, 2022
Level 1
Level 2
Level 3
Total
$
$
— $
—
75,212
75,212 $
175,548 $
4,675
—
180,223 $
— $
—
—
— $
175,548
4,675
75,212
255,435
(1) As of December 31, 2022, commercial paper investments of $131.1 million, U.S. government and agency securities of $4.0 million, and corporate notes of
$2.0 million are included in cash and cash equivalents on the consolidated balance sheets, as the investments had a maturity of three months or less from the date
of purchase on the consolidated balance sheets.
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The Company holds investments in marketable debt securities that are classified and accounted for as cash equivalents or available-for-sale and
are remeasured on a recurring basis. All of the Company’s available-for-sale debt securities are classified on the consolidated balance sheet as cash
equivalents or short-term investments. The following table summarizes the Company’s cash equivalents and investments in available-for-sale debt
securities by significant investment category as of December 31, 2022 (in thousands):
Cash equivalents:
Commercial paper
Corporate notes
U.S. government and agency securities
Total cash equivalents
Short-term investments:
Commercial paper
Corporate notes
U.S. government and agency securities
Total short-term investments
Total
Foreign Currency Translation
Cost
Unrealized gains Unrealized losses
Fair value
$
$
$
$
$
131,075 $
2,013
3,982
137,070 $
44,473 $
2,664
71,342
118,479 $
— $
—
—
— $
— $
—
6
6 $
— $
—
—
— $
— $
(2)
(118)
(120) $
131,075
2,013
3,982
137,070
44,473
2,662
71,230
118,365
255,549 $
6 $
(120) $
255,435
The functional currencies of the Company’s subsidiaries are currencies other than the U.S. dollar. The Company translates assets and liabilities of
the foreign subsidiaries into U.S. dollars at the exchange rate in effect on the balance sheet date. Revenue and expenses of the subsidiaries are translated
into U.S. dollars at the average exchange rate during the period. Gains or losses from these translation adjustments are reported as a separate component of
stockholders’ equity in accumulated other comprehensive gain or loss until there is a sale or complete or substantially complete liquidation of the
Company’s investment in the foreign subsidiary at which time the gains or losses will be realized and included in net income (loss). As of December 31,
2022 and 2021, all foreign currency translation gains (losses) have been unrealized and included in accumulated other comprehensive loss. Accumulated
other comprehensive loss consists entirely of losses or gains from translation of foreign subsidiaries at December 31, 2022 and 2021.
Inventory, Net
Inventories are stated at the lower of cost or net realizable value, with cost computed on a first-in, first-out basis. The Company reduces the
carrying value of inventories for items that are potentially excess, obsolete, or slow-moving based on changes in customer demand, technology
developments, or other economic factors.
The Company capitalizes inventory produced for commercial sale. The Company capitalizes manufacturing costs as inventory following both the
receipt of regulatory approval from regulatory bodies and the Company’s intent to commercialize. Costs associated with developmental products prior to
satisfying the Company’s inventory capitalization criteria are charged to research and development expenses as incurred.
Products that have been approved by certain regulatory authorities may also be used in clinical programs to assess the safety and efficacy of the
products for usage that have not been approved by the FDA or other regulatory authorities. The form of product utilized for both commercial and certain
clinical programs that are identical are included as inventory with an “alternative future use” as defined in authoritative guidance. Component materials and
purchased products associated with clinical development programs are included in inventory and charged to research and development expenses when the
product enters the research and development process and no longer can be used for commercial purposes and, therefore, does not have an “alternative
future use.”
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For products that are under development and have not yet been approved by regulatory authorities, purchased component materials are charged to
research and development expenses when the inventory ownership transfers to the Company.
The Company analyzes inventory levels to identify inventory that may expire prior to sale, inventory that has a cost basis in excess of its net
realizable value, or inventory in excess of expected sales requirements. Although the manufacturing of the Company’s SNM systems is subject to strict
quality control, certain batches or units of product may no longer meet quality specifications or may expire, which would require adjustments to the
Company’s inventory values. The Company also applies judgment related to the results of quality tests that are performed throughout the production
process, as well as the understanding of regulatory guidelines, to determine if it is probable that inventory will be saleable. These quality tests are
performed throughout the pre- and post-production processes, and the Company continually gathers information regarding product quality for periods after
the manufacturing date. The Company’s products currently have a maximum estimated shelf-life range of 12 to 36 months and based on sales forecasts, the
Company expects to realize the carrying value of the product inventory. In the future, reduced demand, quality issues, or excess supply beyond those
anticipated by management may result in a material adjustment to inventory levels, which would be recorded as an increase to cost of sales.
The determination of whether inventory costs will be realizable or not requires estimates by the Company’s management. A critical input in this
determination is future expected inventory requirements based on internal sales forecasts. Management then compares these requirements to the expiry
dates of inventory on hand. To the extent that inventory is expected to expire prior to being sold, management will write down the value of inventory.
As of December 31, 2022, the Company had $30.4 million, $5.7 million, and $19.7 million of finished goods inventory, work-in-process inventory
and raw materials inventory, respectively, net of reserves of $0.5 million. As of December 31, 2021, the Company had $46.8 million, $2.8 million and
$15.3 million of finished goods inventory, work-in-process inventory and raw materials inventory, respectively, net of reserves of $0.2 million.
Customer and Vendor Concentration
As of December 31, 2022 and 2021, there were no customers who accounted for over 10% of the Company’s consolidated accounts receivable. As
of December 31, 2022 and 2021, there was one vendor and no vendor, respectively, who accounted for over 10% of the Company’s consolidated accounts
payable. As of December 31, 2022, 2021, and 2020, there were no customers who accounted for over 10% of the Company’s consolidated net revenue. As
of December 31, 2022, 2021, and 2020, there were three, three, and two vendors, respectively, who accounted for over 10% of the Company’s inventory-
related purchases.
Property and Equipment
Property and equipment are stated at cost less accumulated depreciation. Depreciation is computed using the straight-line method over the
estimated useful lives of the assets, generally between three and seven years. Leasehold improvements are amortized over the lesser of the life of the lease
or the useful life of the improvements. Maintenance and repairs are charged to expense as incurred. When assets are retired or otherwise disposed of, the
cost and accumulated depreciation are removed from the balance sheet and any resulting gain or loss is reflected in operations.
Goodwill
Goodwill represents the excess purchase price over the fair values of both tangible and intangible assets acquired less the liabilities assumed.
Goodwill is tested for impairment at the reporting unit level by comparing the reporting unit’s carrying amount to the fair value of the reporting unit. The
fair values are estimated using an income and discounted cash flow approach. The Company evaluates its goodwill on an annual basis in the fourth quarter
or more frequently if it believes indicators of impairment exist. The Company assesses qualitative factors to determine whether it is more likely than not
that the fair value of a reporting unit is less than its carrying amount or performs an annual impairment test. When tested quantitatively, the Company
compares the fair value of the applicable reporting unit with its carrying value. In making this assessment, management relies on a number of factors,
including expected future operating results, business plans, economic projections, anticipated future cash flows, business trends and declines in the
Company’s market capitalization. The Company estimates the fair value of its reporting unit using a combination of the discounted cash flow and income
approaches. If the carrying amount of a
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reporting unit exceeds the reporting unit’s fair value, the amount by which the carrying value exceeds the fair value is recognized as an impairment loss.
During the year ended December 31, 2022, the Company did not record any impairment charges related to goodwill.
Intangible Assets
Patent license asset
The intangible asset represents exclusive rights to an additional field-of-use on the patent suite within the License Agreement with AMF. The
additional field-of-use was provided in exchange for 50,000 shares of Series A preferred stock, the fair value of which was $1.0 million in 2013. The
intangible asset was recorded at its fair value of $1.0 million at the date contributed. In connection with the IPO, such shares of Series A preferred stock
were converted into common stock. Amortization of this asset is recorded over the shorter of the patent or legal life on a straight-line basis. The weighted-
average amortization period is 8.71 years. The asset has been fully amortized as of December 31, 2022. For additional information, see Note 3.
Exclusive license asset
The intangible asset represents exclusive rights to existing technologies and development services from Micro Systems Engineering, Inc. pursuant
to an agreement entered into on March 2, 2021. The rights and services were provided in exchange for 65,594 shares of common stock, the fair value of
which was $3.6 million upon transfer. The intangible asset was recorded at its fair value of $3.3 million at the date of the agreement, with the difference of
$0.3 million recorded as a vendor credit in accounts payable in the consolidated balance sheets. Amortization of this asset is recorded over the four-year
term of the agreement on a straight-line basis. The Company will review the intangible asset for impairment whenever an impairment indicator exists.
There have been no intangible asset impairment charges to date. For additional information, see Note 3.
Contura acquisition
The intangible assets represent technology, trade names and trademarks, and customer relationships acquired from Contura on February 25, 2021.
The trade names and trademarks have an indefinite life. The straight-line method over the period of estimated benefit is used to amortize technology.
Accounting Standards Codification (ASC) 350-30-35-3 states that customer relationships generally dissipate at a more rapid rate in the earlier periods
following a company’s succession to these relationships, with the rate of attrition declining over time. As such, the accelerated method is used to amortize
customer relationships. The Company reviewed the intangible assets for impairment for this asset group during the year ended December 31, 2022. As
Bulkamid SARL ceased sales operations and did not recognize revenue during the year ended December 31, 2022, and does not expect to recognize
revenue in future periods, the Company wrote off the customer relationships intangible asset of $0.3 million related to this entity. The impairment expense
is recorded within the general and administrative expenses in its consolidated statements of comprehensive loss. For additional information, see Notes 3
and 9.
Impairment of Long-Lived Assets
The Company reviews its long-lived assets for impairment whenever events or changes in circumstances indicate that the carrying amount of an
asset may not be recoverable. Recoverability is measured by comparing the carrying amount to the future net cash flows that the assets are expected to
generate. If said assets are considered to be impaired, the impairment that would be recognized is measured by the amount by which the carrying amount of
the assets exceeds the projected discounted future net cash flows arising from the asset. There have been $0.3 million of impairments of long-lived assets to
date.
Indefinite-lived intangible assets are tested for impairment annually in the fourth quarter of the fiscal year and whenever events or changes in
circumstances indicate that the carrying amount may be impaired. Impairment is calculated as the excess of the asset’s carrying value over its fair value.
Fair value is generally determined using a discounted future cash flow analysis. There have been no impairments to indefinite-lived intangible assets during
the year ended December 31, 2022
Leases
In accordance with Accounting Standards Update (ASU) No. 2016-02, “Leases (Topic 842),” components of a lease should be split into three
categories: lease components, non-lease components, and non-components. The
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fixed and in-substance fixed contract consideration (including any consideration related to non-components) must be allocated based on the respective
relative fair values to the lease components and non-lease components. Entities may elect not to separate lease and non-lease components. Rather, entities
would account for each lease component and related non-lease component together as a single lease component. The Company has elected to account for
lease and non-lease components together as a single lease component for all underlying assets and allocate all of the contract consideration to the lease
component only. Topic 842 allows for the use of judgment in determining whether the assumed lease term is for a major part of the remaining economic
life of the underlying asset and whether the present value of lease payments represents substantially all of the fair value of the underlying asset. The
Company applies the bright line thresholds referenced in Topic 842 to assist in evaluating leases for appropriate classification between operating and
finance leases. The aforementioned bright lines are applied consistently to the Company’s entire portfolio of leases.
Operating lease right-of-use (ROU) assets and operating lease liabilities are recognized based on the present value of the future minimum lease
payments over the lease term at commencement date. As the Company’s leases do not provide an implicit rate, the Company uses its incremental
borrowing rate, which is the rate for a fully collateralized amortizing loan with the same maturity as the lease term in similar economic environment, based
on the information available at commencement date in determining the present value of future payments. The operating lease ROU assets also includes any
lease payments made and excludes lease incentives and initial direct costs incurred. The lease terms may include options to extend or terminate the lease
when it is reasonably certain that the Company will exercise that option. Lease expense for minimum lease payments is recognized on a straight-line basis
over the lease term.
Research and Development
Research and development costs are charged to operations as incurred. Research and development costs include salary and personnel-related costs,
costs of clinical studies and testing, royalty expense, supplies and materials, and outside consultant costs.
Advertising Expense
The Company expenses advertising costs as they are incurred. During the years ended December 31, 2022, 2021, and 2020, advertising expense
totaled $20.6 million, $7.8 million and $2.9 million, respectively, and are recorded within the sales and marketing expenses in its consolidated statements of
comprehensive loss.
Income Taxes
The Company accounts for income taxes using the asset and liability method to compute the difference between the tax basis of assets and
liabilities and the related financial amounts, using currently enacted tax rates. The Company has net deferred tax assets in certain jurisdictions. The
realization of these deferred tax assets is dependent upon the Company’s ability to generate sufficient taxable income in future years. Valuation allowances
are established, when necessary, to reduce deferred tax assets to the amount that more likely than not will be realized. The Company evaluates the
recoverability of the deferred tax assets annually and maintains a full valuation allowance on its U.S. net deferred tax assets. The Company recognizes the
tax benefit from an uncertain tax position only if it is more likely than not that the tax position will be sustained on examination by taxing authorities, based
on the technical merits of the position. The Company is subject to transfer pricing and other tax regulations designed to ensure that appropriate levels of
income are reported as earned by the Company’s U.S. and foreign entities and are taxed accordingly. In the normal course of business, the Company is
audited by federal, state and foreign tax authorities, and subject to inquiries from those tax authorities regarding the amount of taxes due. These inquiries
may relate to the timing and amount of deductions and the allocation of income among various tax jurisdictions. The Company’s policy is to recognize
interest and penalties related to unrecognized tax benefits, if any, in income tax expense.
Stock-Based Compensation
The Company measures the cost of employee and non-employee services in exchange for an award of equity instruments based on the grant-date
fair value of the award and recognizes compensation cost over the requisite service period (typically the vesting period), generally three or four years.
Forfeitures are estimated at the time of the grant and revised in subsequent periods to reflect differences between the estimates and the number of
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shares that actually become exercisable. The Company uses the Black-Scholes option pricing model to determine the fair value of stock options (as of the
date of grant) that have service conditions for vesting. Stock options and restricted shares awards vest based on service conditions, typically over three or
four years.
The Company also grants shares of performance-based restricted stock units that typically vest after one year only if the Company has also
achieved certain performance objectives as defined and approved by the Company’s board of directors. The fair value of performance awards is determined
based on the Company’s stock price at the date of grant and expensed over the performance period based on the probability of achieving the performance
objectives. If such targets are not met or service is not rendered for the requisite service period, no compensation cost is recognized, and any recognized
compensation cost in prior periods will be reversed. In addition, the Company also grants market-based restricted stock units that have combined market
conditions and service conditions for vesting, for which the Company uses the Monte Carlo valuation model to value equity awards (as of the date of
grant). Compensation cost is not adjusted if the market condition is not met, as long as the requisite service is provided.
Net Loss per Share of Common Stock
Basic net loss per share of common stock is calculated by dividing the net loss attributable to common stockholders by the weighted-average
number of shares of common stock outstanding during the period, without consideration for potentially dilutive securities. Diluted net loss per share is
computed by dividing the net loss attributable to common stockholders by the weighted-average number of shares of common stock and potentially dilutive
securities outstanding for the period. For purposes of the diluted net loss per share calculation, common stock options, unvested RSAs and RSUs are
considered to be potentially dilutive securities. Because the Company has reported a net loss in all periods presented, diluted net loss per share of common
stock is the same as basic net loss per share of common stock for those periods.
For the years ended December 31, 2022, 2021, and 2020, there were 2,328,525, 2,444,444, and 2,300,982 potentially dilutive weighted-average
shares, respectively, that were not included in the computation of diluted weighted-average shares of common stock and common stock equivalent shares
outstanding because their effect would have been antidilutive given the Company’s net loss.
Segment Reporting
Operating segments are defined as components of an entity for which separate financial information is available and that is regularly reviewed by
the Chief Operating Decision Maker (CODM) in deciding how to allocate resources to an individual segment and in assessing performance. The
Company’s CODM is its Chief Executive Officer. The Company has determined it operates in one segment, the development and commercialization of
innovative and minimally invasive products to treat bladder and bowel dysfunction. Geographically, the Company sells over 90% of its products to
customers in the United States. Segment information is consistent with how management reviews the business, makes investing and resource allocation
decisions and assesses operating performance.
Recent Accounting Pronouncements
We have reviewed and considered all recent accounting pronouncements that have not yet been adopted and believe there are none that could
potentially have a material impact on our business practices, financial condition, results of operations, or disclosures.
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Note 2. Property and Equipment, Net
Property and equipment, net consists of the following (in thousands) at:
Equipment
Computer hardware and software
Tools and molds
Leasehold improvements
Furniture and fixtures
Construction in progress
Less: accumulated depreciation and amortization
December 31,
2022
2021
$
$
2,645 $
3,282
1,735
4,449
1,810
413
14,334
(7,536)
6,798 $
2,429
2,450
1,579
4,372
1,502
127
12,459
(5,544)
6,915
Depreciation and amortization expense of property and equipment was $2.3 million, $1.9 million, and $1.6 million for the years ended
December 31, 2022, 2021, and 2020, respectively.
Note 3. Goodwill and Intangible Assets
The change in the carrying amount of goodwill during the years ended December 31, 2022 and 2021 included the following (in thousands):
December 31, 2020
February 25, 2021 Acquisition
Foreign currency translation adjustment
December 31, 2021
Foreign currency translation adjustment
December 31, 2022
$
$
—
109,786
(4,276)
105,510
(11,096)
94,414
Intangible assets as of December 31, 2022 included the following (in thousands):
Patent license asset
Exclusive license
asset
Technology
Trade names and
trademarks
Customer
relationships
Weighted-Average
Amortization Period
8.71 years
4 years
12 years
Indefinite
12 years
Gross
Carrying
Amount
Accumulated
Amortization
Impairment
Foreign currency
translation
adjustment
Intangible Assets,
Net
December 31, 2022
$
1,000 $
(1,000) $
— $
— $
3,300
81,100
19,700
(1,540)
(12,496)
—
—
—
—
—
(9,141)
(2,398)
11,400
116,500 $
$
(2,393)
(17,429) $
(287)
(287) $
(992)
(12,531) $
—
1,760
59,463
17,302
7,728
86,253
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Intangible asset as of December 31, 2021 included the following (in thousands):
Patent license asset
Exclusive license asset
Technology
Trade names and trademarks
Customer relationships
Weighted-Average
Amortization Period
8.71 years
4 years
12 years
Indefinite
12 years
$
$
December 31, 2021
Gross Carrying
Amount
Accumulated
Amortization
Foreign currency
translation
adjustment
Intangible Assets,
Net
1,000 $
3,300
81,100
19,700
11,400
116,500 $
(919) $
(660)
(5,668)
—
(799)
(8,046) $
— $
—
(1,424)
(365)
(196)
(1,985) $
81
2,640
74,008
19,335
10,405
106,469
The Company recorded expense for the amortization of intangible assets of $9.4 million, $7.2 million, and $0.1 million, respectively, during the
years ended December 31, 2022, 2021, and 2020. The estimated future amortization expense as of December 31, 2022, is as follows (in thousands):
2023
2024
2025
2026
2027
Note 4. Commitments and Contingencies
Operating Leases
$
9,085
8,962
7,927
7,783
7,645
In August 2014, the Company entered into a five-year operating lease for approximately 12,215 square feet of office space beginning on
November 1, 2014, and expiring on October 31, 2019. In June 2019, the lease was amended to extend the expiration date to October 31, 2020. In
September 2020, the lease was amended to extend the expiration date to July 31, 2022, and in December 2021, the lease was amended to extend the
expiration date to January 31, 2028. Upon the execution of the amendments, which were deemed to be a lease modification, the Company reassessed the
lease liability using the incremental borrowing rate for a collateralized asset of the same remaining term at the modification date and recorded ROU assets
for the same amount. The Company also reassessed the lease classification and concluded that the lease continues to be an operating lease. Under the terms
of the lease, the Company is responsible for taxes, insurance, and maintenance expense. The lease contains certain scheduled rent increases. Rent expense
is recognized on a straight-line basis over the expected lease term.
The Company entered into an operating lease for approximately 25,548 square feet of office space beginning on August 1, 2018, and expiring on
October 31, 2027. Under the terms of the lease, the Company is responsible for taxes, insurance, and maintenance expense. The lease contains certain
scheduled rent increases. Rent expense is recognized on a straight-line basis over the expected lease term. The Company has a renewal option to extend the
term of the lease for a period of five years beyond the initial term. Under the terms of the lease, the base rent payable with respect to each renewal term will
be equal to the prevailing market rental rent as of the commencement of the applicable renewal term. In the event of a default of certain of the Company’s
obligations under the lease, the Company’s landlord would have the right to terminate the lease.
In June 2019, the Company entered into an eight-year operating lease for approximately 32,621 square feet of office space beginning on January
15, 2020 and expiring on January 31, 2028. The Company uses these premises as its new principal executive offices and for general office space. The
Company is utilizing its other currently-leased spaces to conduct the training of its sales team and for manufacturing purposes. Under the terms of the lease,
the Company is responsible for taxes, insurance, and maintenance expense. The lease contains certain scheduled rent increases. Rent expense is recognized
on a straight-line basis over the expected lease term. The Company has a
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renewal option to extend the term of the lease for a period of five years beyond the initial term. Under the terms of the lease, the base rent payable with
respect to each renewal term will be equal to the prevailing market rental rent as of the commencement of the applicable renewal term. In the event of a
default of certain of the Company’s obligations under the lease, the Company’s landlord would have the right to terminate the lease.
In August 2020, the Company entered into a 38-month operating lease for approximately 5,693 square feet of warehouse space beginning on
October 15, 2020 and expiring on December 31, 2023. The Company uses these premises for general warehouse space.
In March 2022, the Company entered into an 18-month operating lease for approximately 3,276 square feet of warehouse space beginning on July
1, 2022 and expiring on December 31, 2023. The Company uses these premises for general warehouse space.
During the years ended December 31, 2022, 2021, and 2020, ROU assets obtained in exchange for new operating lease liabilities were $0.1
million, $1.0 million, and $3.8 million, respectively. As of December 31, 2022 and 2021, the ROU assets had a balance of $6.2 million and $7.1 million,
respectively. The operating lease ROU assets are included within the Company’s non-current other assets, and lease liabilities are included in current or
noncurrent liabilities in the Company’s consolidated balance sheets. During the years ended December 31, 2022, 2021, and 2020, cash paid for amounts
included in operating lease liabilities was $2.1 million, $2.0 million, and $1.5 million, respectively. Amortization of the ROU assets was $1.0 million, $1.0
million, and $0.9 million for the years ended December 31, 2022, 2021, and 2020, respectively. As of December 31, 2022 and 2021, the weighted-average
remaining lease term for the Company’s operating leases was 4.9 years and 5.9 years, respectively. The weighted-average incremental borrowing rate for a
collateralized asset of the same remaining term used to determine the present value of the Company’s operating leases’ future payments was 7.1% and
7.1%, respectively.
Total lease costs for the years ended December 31, 2022, 2021, and 2020 are as follows (in thousands):
Lease cost
Operating lease cost
Short-term lease cost
Variable lease cost
Total lease cost
2022
December 31,
2021
2020
$
$
2,131 $
80
203
2,414 $
2,107 $
95
191
2,393 $
Payments of operating lease liabilities as of December 31, 2022, are as follows (in thousands):
2023
2024
2025
2026
2027
Thereafter
Less: imputed interest
Less: operating lease liability, current portion
Operating lease liability, net of current portion
92
$
$
1,991
95
179
2,265
2,162
2,066
2,150
2,239
2,165
115
10,897
(1,780)
9,117
(1,562)
7,555
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License Agreement
In October 2013, the Company entered into the License Agreement, pursuant to which AMF, a Company stockholder, licensed the Company
certain patents and know-how (collectively, the AMF IP) relating to, in relevant part, an implantable pulse generator and related system components in
development by AMF as of that date, in addition to any peripheral or auxiliary devices, including all components, that when assembled, comprise such
device, excluding certain implantable pulse generators (collectively, the AMF Licensed Products). Under the License Agreement, for each calendar year
beginning in 2018, the Company is obligated to pay AMF a royalty on an AMF Licensed Product-by-AMF Licensed Product basis if one of the following
conditions applies: (i) one or more valid claims within any of the patents licensed to the Company by AMF covers such AMF Licensed Products or the
manufacture of such AMF Licensed Products or (ii) for a period of 12 years from the first commercial sale anywhere in the world of such AMF Licensed
Product, in each case. The foregoing royalty is calculated as the greater of (a) 4% of all net revenue derived from the AMF Licensed Products, and (b) the
Minimum Royalty, payable quarterly. The Minimum Royalty automatically increases each year after 2018, subject to a maximum amount of $200,000 per
year. The Company recorded related royalties of $3.3 million, $6.3 million, and $4.4 million during the years ended December 31, 2022, 2021, and 2020,
respectively. Royalty expense is included in operating expenses in the consolidated statements of comprehensive loss. Accrued royalties of $0.6 million and
$1.8 million as of December 31, 2022 and 2021, respectively, are included within accrued liabilities in the Company’s consolidated balance sheets. Royalty
expense is declining because the Company’s F15 recharge-free SNM device is not covered by any AMF patents licensed to the Company and is therefore
not an AMF Licensed Product that requires the payment of a royalty to AMF.
Legal Matters
On November 4, 2019, Medtronic, Inc., Medtronic Puerto Rico Operations Co., Medtronic Logistics LLC and Medtronic USA, Inc. (collectively,
the Medtronic Affiliates) filed a complaint against the Company in the U.S. District Court for the Central District of California, Case No. 8:19-cv-2115,
and amended the complaint on November 26, 2019. The Company refers to this matter as the Medtronic Litigation. The complaint asserts that the
Company’s rechargeable SNM system infringes U.S. Patent Nos. 8,036,756, 8,626,314, 9,463,324 and 9,821,112 held by the Medtronic Affiliates, and the
amended complaint further includes the additional patents 8,738,148; 8,457,758; and 7,774,069 (collectively, the Medtronic Patents). The Medtronic
Litigation requests customary remedies for patent infringement, including (i) a judgment that the Company has infringed and is infringing the Medtronic
Patents, (ii) damages, including treble damages for willful infringement, (iii) a permanent injunction preventing the Company from infringing the
Medtronic Patents, (iv) attorneys’ fees, and (v) costs and expenses. The Company believes the allegations are without merit and is vigorously defending
itself against them. The Company is unable to predict the likelihood of success of the claims of the Medtronic Affiliates against the Company or to quantify
any risk of loss. The Medtronic Litigation could last for an extended period of time and require the Company to dedicate significant financial resources and
management resources to its defense. An adverse ruling against the Company could materially and adversely affect its business, financial position, results
of operations or cash flows and could also result in reputational harm. Even if the Company is successful in defending against these claims, the Medtronic
Litigation could result in significant costs, delays in future product developments, reputational harm or other collateral consequences. The Company is
currently engaged in discovery in the Medtronic Litigation. A jury trial is scheduled in the Medtronic Litigation for April 2023.
In addition to the Medtronic Litigation, the Company is and may continue to be involved in claims, legal proceedings, and investigations arising
out of its operations in the normal course of business.
Note 5. Long-Term Debt
In February 2018, the Company entered into the Loan and Security Agreement with Silicon Valley Bank, providing for a term loan (the Term
Loan).
In January 2021, the principal amount, accrued interest, accrued loan fees, and prepayment fees related to the Term Loan were paid in full. The
unamortized debt issuance costs of $0.4 million were expensed and recognized as interest expense.
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In February 2021, the Company entered into another Loan and Security Agreement (the Loan and Security Agreement) with Silicon Valley Bank,
under which the Company obtained a loan in the principal amount of $75 million.
In June 2021, the principal amount, accrued interest, accrued loan fees, and prepayment fees related to this loan were paid in full. The unamortized
debt issuance costs of $4.4 million were expensed and recognized as interest expense.
Note 6. Stockholders’ Equity
Preferred Stock
As of December 31, 2022, the Company is authorized to issue 10,000,000 shares of preferred stock with a par value of $0.0001 per share. No
preferred stock is issued or outstanding as of December 31, 2022.
Common Stock
The following summarizes the rights of holders of our common stock:
Voting
The holders of our common stock are entitled to one vote per share. The number of authorized shares of common stock may be increased or
decreased (but not below the number of shares thereof then outstanding) by the affirmative vote of the holders of a majority of the voting power of our
capital stock entitled to vote, irrespective of the provisions of Section 242(b)(2) of the DGCL.
Dividends
Subject to preferences that may be applicable to the holders of outstanding shares of preferred stock and subject to applicable law, dividends may
be declared and paid on the holders of our common stock when and as determined by our board of directors out of assets legally available for dividends.
As a Delaware corporation, the Company will be subject to certain restrictions on dividends under the DGCL. Generally, a Delaware corporation
may only pay dividends either out of “surplus” or out of the current or the immediately preceding year’s net profits. Surplus is defined as the excess, if any,
at any given time, of the total assets of a corporation over its total liabilities and statutory capital. The value of a corporation’s assets can be measured in a
number of ways and may not necessarily equal their book value.
Liquidation Rights
Upon our voluntary or involuntary liquidation, dissolution or winding up, after satisfaction of all our liabilities and the payment of any liquidation
preference of any outstanding preferred stock, the holders of shares of common stock will be entitled to share in all of our assets legally remaining for
distribution after payment of all debt and other liabilities, subject to preferences that may be applicable to the holders of outstanding shares of preferred
stock.
Redemption Rights
There are no redemption or sinking fund provisions applicable to our common stock.
Preemptive Rights and Conversion Rights
There are no preemptive or conversion rights applicable to our common stock.
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Stock-Based Compensation Expense
Stock-based compensation expense included in the Company’s consolidated statements of comprehensive loss is allocated as follows (in
thousands):
Research and development
General and administrative
Sales and marketing
Stock Option Activity
2014 Stock Option Plan
2022
Years Ended December 31,
2021
2020
$
$
6,734 $
7,965
17,319
32,018 $
5,980 $
8,079
11,105
25,164 $
3,457
5,852
5,786
15,095
In 2014, the Company established its 2014 Stock Option Plan (the 2014 Plan), which provides for the granting of stock options to employees,
directors, and consultants of the Company. The 2018 Omnibus Incentive Plan was adopted upon our IPO and replaced the 2014 Stock Option Plan for
future grants. As of December 31, 2022 and 2021, there were no stock options available for grant under the 2014 Plan.
2018 Omnibus Incentive Plan
On October 18, 2018, the Company adopted the 2018 Omnibus Incentive Plan (the 2018 Plan), under which the Company may grant cash and
equity incentive awards to eligible service providers to attract, motivate and retain the talent for which it competes. The 2018 Plan provides for awards
based on shares of the Company’s common stock. Subject to adjustment by the Company’s board of directors, the total number of shares authorized to be
awarded under the 2018 Plan may not exceed 7,088,581. As of December 31, 2022 and 2021, there were 2,694,622 and 950,354 shares available for grant
under the 2018 Plan, respectively.
The Company had shares of common stock reserved for future issuance as follows at:
Options outstanding under the 2014 Plan
Options and restricted stock units outstanding under the 2018 Plan
Options and restricted stock-based awards remaining under the 2018 Plan for future issuance
December 31,
2022
2021
184,104
1,045,924
2,694,622
3,924,650
277,505
1,400,851
950,354
2,628,710
The fair value of each stock option is measured as of the date of grant, and compensation expense is recognized over the period during which the
recipient renders the required services to the Company (typically the vesting period). Stock-based compensation expense recognized is based on the
estimated number of stock options that are expected to ultimately become exercisable. Forfeitures are estimated at the time of the grant and revised in
subsequent periods to reflect differences between the estimates and the number of shares that become exercisable.
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The option awards issued under the 2014 and 2018 Plans were measured based on fair value. The Company’s fair value calculations were made
using the Black-Scholes option pricing model with the following assumptions:
Expected term (in years)
Stock volatility
Risk-free interest rate
Dividend rate
2022
—
—
—
—
Years Ended December 31,
2021
5.46 - 6.00
63.49%
0.53% - 1.16%
—
2020
6.05
72.01%
1.37%
—
The Company used the simplified method of determining the expected term of stock options as the Company believes this represents the best
estimate of the expected term of a new option. The expected stock price volatility assumption was determined by examining the historical volatilities for
industry peers, as the Company did not have sufficient trading history for the Company’s common stock. The Company will continue to analyze the
historical stock price volatility and expected term assumption as more historical data for the Company’s common stock becomes available. The risk-free
interest rate assumption is based on the U.S. Treasury instruments, whose term was consistent with the expected term of the Company’s stock options. The
expected dividend assumption is based on the Company’s history and expectation of dividend payouts. The assumptions regarding the expected term of the
options and the expected volatility of the stock price are subjective, and these assumptions have a significant effect on the estimated fair value amounts.
There were no stock option grants for the year ended December 31, 2022. The weighted-average grant date fair value of options granted was $32.93 and
$18.56 for the years ended December 31, 2021 and 2020, respectively.
As of December 31, 2022 and 2021, there was $1.8 million and $6.7 million, respectively, of total unrecognized compensation cost related to
unvested stock options that is expected to be recognized over a weighted-average period of approximately 1.0 year and 1.6 years, respectively.
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The following table summarizes stock option activity under the 2014 and 2018 Plans (in thousands, except share and per share data):
Outstanding at December 31, 2019
Options granted
Options exercised
Options forfeited
Outstanding at December 31, 2020
Options granted
Options exercised
Options forfeited
Outstanding at December 31, 2021
Options exercised
Options forfeited
Outstanding at December 31, 2022
Options exercisable at December 31, 2022
_____________________________________________
Number of Options
Weighted-Average
Exercise Price Per
Share
Aggregate Intrinsic
Value
2,847,101 $
5,000
(767,792)
(129,066)
1,955,243
46,000
(522,495)
(50,856)
1,427,892
(364,352)
(16,930)
1,046,610 $
927,595 $
13.22
29.03
5.05 $
20.20
16.01
58.07
12.60 $
29.64
18.13
15.54 $
31.80
18.81 $
17.68 $
25,066
(1)
24,455
(1)
18,251
(1)
45,762
(2)
41,604
(2)
(1) Represents the total difference between the Company’s closing stock price at the time of exercise and the stock option exercise price, multiplied by the number of
options exercised.
(2) Represents the total difference between the Company’s closing stock price on the last trading day of 2022 and the stock option exercise price, multiplied by the
number of in-the-money options as of December 31, 2022. The amount of intrinsic value will change based on the fair market value of the Company’s stock.
The weighted-average remaining contractual term of options outstanding and exercisable is 6.1 years and 6.9 years at December 31, 2022 and
2021, respectively.
Restricted Shares Awards Activity
As of December 31, 2022 and 2021, there was $54.0 million and $42.5 million, respectively, of total unrecognized compensation cost related to
unvested restricted shares awards that is expected to be recognized over a weighted-average period of approximately 2.3 years and 3.0 years, respectively.
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The following table summarizes restricted shares awards activity:
Outstanding at December 31, 2019
Restricted shares awards granted
Restricted shares awards vested
Restricted shares awards forfeited
Outstanding at December 31, 2020
Restricted shares awards granted
Restricted shares awards vested
Restricted shares awards forfeited
Outstanding at December 31, 2021
Restricted shares awards granted
Restricted shares awards vested
Restricted shares awards forfeited
Outstanding at December 31, 2022
Restricted Stock Units Activity
Number of
Restricted Shares
Awards
Weighted-Average
Fair Value Per Share
at Grant Date
586,166 $
502,500
(174,890)
(96,593)
817,183
638,936
(235,560)
(118,525)
1,102,034
683,354
(351,946)
(112,576)
1,320,866 $
23.59
37.68
23.29
28.83
31.70
57.90
31.19
40.33
46.07
56.69
42.15
50.50
52.23
As of December 31, 2022 and 2021, there was $1.3 million and $1.9 million, respectively, of total unrecognized compensation cost related to
unvested restricted stock units that is expected to be recognized over a weighted-average period of approximately 0.8 years and 0.9 years, respectively.
The following table summarizes restricted stock units activity:
Outstanding at December 31, 2019
Restricted stock units granted
Restricted stock units vested
Restricted stock units forfeited
Outstanding at December 31, 2020
Restricted stock units granted
Restricted stock units vested
Outstanding at December 31, 2021
Restricted stock units granted
Restricted stock units vested
Outstanding at December 31, 2022
Number of
Restricted Stock
Units
Weighted-Average
Fair Value Per Share
at Grant Date
248,104 $
8,000
(46,336)
(2,667)
207,101
212,417
(169,054)
250,464
201,884
(268,930)
183,418 $
21.48
29.03
14.19
14.19
23.49
43.62
19.89
42.99
38.75
35.88
48.74
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Table of Contents
Note 7. Income Taxes
The components of net (loss) income before income tax expense were as follows (in thousands):
Domestic
Foreign
Total
2022
Years Ended December 31,
2021
2020
$
$
(24,466) $
(37,850)
(62,316) $
(56,105) $
(23,180)
(79,285) $
(54,994)
80
(54,914)
The components of the income tax expense (benefit) were as follows (in thousands):
Current:
Federal
State
Foreign
Total current income tax expense
Deferred:
Federal
State
Foreign
Total deferred income tax (benefit) expense
Total
2022
Years Ended December 31,
2021
2020
$
$
$
$
$
— $
76
174
250 $
— $
—
(2,868)
(2,868) $
(2,618) $
— $
211
26
237 $
(422) $
(117)
1,084
545 $
782 $
The reconciliation between the Company’s effective tax rate and the statutory tax rate is as follows:
Tax at statutory federal rate
State tax, net of federal benefit
Excess tax benefits related to stock-based compensation
Non-deductible stock-based compensation
Tax rate change
Net operating loss adjustments
Section 382 limitation
R&D tax credit, net of reserve
Change in valuation allowance
Change in fair value of contingent consideration
Other
Effective tax rate
2022
Years Ended December 31,
2021
2020
21.0 %
1.0 %
8.3 %
(1.7)%
1.0 %
— %
— %
4.1 %
(19.6)%
(7.3)%
(2.6)%
4.2 %
21.0 %
3.8 %
9.4 %
(1.4)%
(5.2)%
(7.9)%
— %
6.1 %
(24.5)%
— %
(2.3)%
(1.0)%
—
1
—
1
—
—
—
—
1
21.0 %
7.0 %
10.3 %
— %
— %
— %
— %
(4.5)%
(36.8)%
— %
3.0 %
— %
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Our effective tax rate was 4.2% for the year ended December 31, 2022, compared to an effective tax rate of (1.0)% for the year ended
December 31, 2021 and 0.0% for the year ended December 31, 2020. The effective tax rates for the periods presented are primarily comprised of U.S. and
foreign statutory taxes, excess tax benefits related to stock-based compensation, change in foreign statutory income tax rates, change in fair value of the
contingent consideration, and a change in valuation allowance. The difference in the effective tax rate of 4.2% for the year ended December 31, 2022 as
compared to the effective tax rate of (1.0)% for the year ended December 31, 2021 was primarily due to higher net operating loss adjustments and change
in valuation allowance during the year ended December 31, 2021.
Deferred income taxes reflect the net tax effects of temporary differences between the carrying amounts of assets and liabilities for financial
reporting purposes and the amounts used for income tax purposes. Significant components of the Company’s deferred tax assets and liabilities are as
follows (in thousands) as of:
Deferred Tax Assets:
Stock-based compensation
Depreciation and amortization
Lease liabilities
Net operating loss carryforwards
Research and development credit carryforwards
Interest expense limitation carryforwards
Other
Total deferred tax assets
Less: valuation allowance
Total net deferred tax assets
Deferred Tax Liabilities:
ROU assets
Intangibles
Total deferred tax liabilities
Net deferred tax liabilities
December 31,
2022
2021
4,855 $
(196)
2,169
76,013
7,332
5,457
10,209
105,839
(96,751)
9,088 $
(1,464) $
(24,036)
(25,500) $
5,367
7
895
74,744
4,865
2,518
2,895
91,291
(85,061)
6,230
—
(25,447)
(25,447)
(16,412) $
(19,217)
$
$
$
$
$
At December 31, 2022, the Company had U.S. federal and foreign net operating loss (NOL) carryforwards of approximately $270.3 million and
$9.6 million, respectively. Of the U.S. federal NOLs, $51.5 million will expire between 2033 and 2037 and the remainder will carryover indefinitely. The
Company had U.S. state NOLs of $254.6 million, which will expire between 2033 and 2042. Under California Assembly Bill 85, effective June 29, 2020,
net operating loss deductions were suspended for tax years beginning in 2020, 2021, and 2022 and the carry forward periods of any net operating losses not
utilized due to such suspension were extended. The foreign net operating loss carryforwards have an indefinite carryforward period.
The Company accounts for income taxes according to ASC 740, “Income Taxes.” The Company periodically evaluates whether a portion or all of
its deferred tax assets will be recovered. The Company records a valuation allowance against deferred tax assets if and to the extent it is more likely than
not that they will not be recovered. In evaluating the need for a valuation allowance, the Company weighs all relevant positive and negative evidence,
including among other factors, historical financial performance, forecasts of income over the applicable carryforward periods, and the market environment,
with each consideration weighted based on its reliability. The Company continues to maintain a full valuation allowance against its otherwise recognizable
U.S. deferred income tax assets as of December 31, 2022 and 2021. The Company has determined, after evaluating all positive and
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negative historical and prospective evidence, that it is more likely than not that the deferred income tax assets will not be realized. The valuation allowance
increased by $11.7 million for the year ended December 31, 2022, from $85.1 million to $96.8 million. This increase in the valuation allowance during the
year ended December 31, 2022, was largely attributable to losses incurred in the U.S. jurisdiction. The Company’s NOL carryforwards were generated
from domestic and foreign operations.
Pursuant to Sections 382 and 383 of the Internal Revenue Code of 1986, as amended (the Internal Revenue Code), use of the Company’s NOL
carryforwards may be limited if the Company experiences a cumulative change in ownership of greater than 50% in a rolling three-year period. The
Company performed an analysis of changes in ownership for purposes of these Internal Revenue Code sections. Based on the study performed in 2020, the
Company determined that an ownership change occurred in 2014, 2018 and 2019. The total reduction to the net operating loss carryforwards and R&D
credit was $12.2 million and $1.5 million, respectively. Based on the studies performed in 2022 and 2021, the Company determined that an ownership
change did not occur in 2022 and 2021. The total reduction of the net operating loss carryforwards was offset by valuation allowance, and there was no
impact to tax expense related to the limitation. Future ownership changes could impact the Company’s ability to utilize NOL carryforwards.
The Company applies the provisions of FASB ASC 740-10, “Accounting for Uncertainty in Income Taxes.” ASC 740-10 prescribes a
comprehensive model for the recognition, measurement, presentation and disclosure in financial statements of any uncertain tax positions that have been
taken or are expected to be taken on a tax return. The Company has identified unrecognized tax benefits or uncertain tax positions. There has been a
liability on uncertain tax positions recorded on the financial statements as of December 31, 2022. The Company does not expect that its assessment
regarding unrecognized tax benefits and uncertain tax positions will materially change over the following 12 months.
A reconciliation of the beginning and ending balances of unrecognized tax benefits is as follows (in thousands):
Balance at December 31, 2020
Additions based on tax positions related to the current year
Additions from business combination
Deductions for tax positions taken in prior years
Balance at December 31, 2021
Additions based on tax positions related to the current year
Deductions for tax positions taken due to settlement
Balance at December 31, 2022
$
$
2,491
528
1,782
(1,397)
3,404
574
(1,603)
2,375
As of December 31, 2022, the total unrecognized tax benefits was $2.4 million, of which, if recognized, $0.1 million would affect the annual
effective tax rate. Due to the conclusion of foreign statutory audits, there was a release of uncertain tax positions. There were no interest or penalties to be
recognized for the tax years ended December 31, 2022 and 2020. As of December 31, 2021, the Company has accumulated $0.4 million in both interest and
penalties associated with uncertain tax positions.
The Company has net operating loss and research and development credit carryforwards which may be subject to examination by taxing
authorities. As of December 31, 2022, tax years beginning with the year ended December 31, 2018 remain subject to examination by the Internal Revenue
Service and certain U.S. state jurisdictions. As of December 31, 2022, tax years beginning with the years ended December 31, 2016, December 31, 2018,
and December 31, 2018 remain subject to examination by the German, French, and the U.K. tax authorities, respectively. The Company is not currently
under audit by any taxing authority.
Note 8. Employee Benefit Plan
The Company sponsors a defined contribution retirement savings plan under Section 401(k) of the Internal Revenue Code. This plan covers all
U.S. employees who meet minimum age and service requirements, and allows participants to defer a portion of their annual compensation on a pre- or post-
tax basis. Contributions to the plan by
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the Company may be made at the discretion of the board of directors. During the years ended December 31, 2022, 2021, and 2020, the Company
contributions to the plan amounted to $2.1 million, $1.9 million, and $1.6 million, respectively.
Note 9. Acquisition
On February 25, 2021, the Company acquired all issued and outstanding shares of Contura Limited (Contura) through a Share Purchase
Agreement. As a result of the acquisition, the Company acquired a 100% equity interest in Contura.
The Company accounted for the acquisition as a business combination pursuant to ASC 805, “Business Combinations”. In accordance with ASC
805, fair values are assigned to tangible and identifiable intangible assets acquired and liabilities assumed at the acquisition date based on the information
that was available as of the acquisition date. The Company believes that the information available provides a reasonable basis for estimating the fair values
of assets acquired and liabilities assumed for the acquisition.
The purchase price consideration for the acquisition totaled $204.7 million, of which $141.4 million was in the form of cash and $55.7 million was
in the form of 1,096,583 shares of the Company’s common stock. Additionally, a payment of $35 million may be paid to Contura if the Company is able to
generate $50 million in Bulkamid sales within a 12-month period before December 31, 2024. As the additional payment is contingent on future sales, an
estimate of fair value was initially assessed to be $7.6 million which was considered part of the purchase price consideration and was recorded as other
long-term liabilities in the consolidated balance sheet. The cash consideration paid for the acquisition was funded by existing cash on hand.
The following table presents the purchase price allocation of Contura assets acquired and liabilities assumed, based on their estimated fair values
as of the February 25, 2021 acquisition date (in thousands):
Assets Acquired
Cash and cash equivalents
Accounts receivable
Inventory
Prepaid expenses and other current assets
Property and equipment
Other assets
Intangible assets
Total assets acquired
Liabilities Assumed
Accounts payable
Accrued liabilities
Accrued compensation and benefits
Lease liability
Debt
Deferred tax liabilities
Total liabilities assumed
Net assets acquired
Purchase price consideration
Goodwill
102
Purchase Price
Allocation
593
1,688
988
115
52
108
112,200
115,744
209
820
315
86
122
19,286
20,838
94,906
204,692
109,786
$
$
Table of Contents
Intangible assets
Identified intangible assets consist of technology, trade names and trademarks, and customer relationships. The fair value of intangible assets and
the determination of their respective useful lives were made in accordance with ASC 805 and are outlined in the table below:
Technology
Trade names and trademarks
Customer relationships
Fair Value
(in thousands)
$
$
$
81,100
19,700
11,400
Useful Life
12 years
Indefinite
12 years
Intangible assets were valued using models and approaches best suited for the asset type.
Technology was valued using the Multi-Period Excess Earnings Method (MPEEM), which calculates economic benefits by determining the
income attributable to an intangible asset after returns are subtracted for contributory assets. Assumptions in the MPEEM include projected revenue growth
rates, future margins, royalty rate indication, and tax rate.
Trade names and trademarks were valued using the Relief from Royalty Method. The relief from royalty method is a variant of the discounted
cash flow method, which is a form of the income approach. It is based on the premise that ownership of the intangible asset relieves the need to pay a
licensing fee for the ability to use the asset. Assumptions include a discount rate, tax rate, royalty rate indication, long-term growth rate, and implied profit
split time period.
Customer relationships were valued using the distributor method. The distributor method was utilized as the asset was determined to be a
secondary intangible asset and the Company’s product could be sold through distributors. Assumptions used in the distributor method include projected
revenue growth rates, future margins, rate of customer retention, and an appropriate discount rate.
Intangible assets will be amortized based on their useful life. $8.4 million and $6.5 million in amortization expense relating to these intangible
assets was recognized during the years ended December 31, 2022 and 2021, respectively, in the consolidated statements of comprehensive loss. The
unamortized balance as of December 31, 2022 and 2021 was $84.5 million and $103.7 million, respectively. The total weighted-average original
amortization period for the acquired finite-lived intangible assets is 12 years.
Goodwill
Goodwill is calculated as the excess of the consideration transferred over the fair value of the identifiable net assets acquired in a business
combination and represents the future economic benefits expected to arise from anticipated synergies and intangible assets acquired that do not qualify for
separate recognition, including an assembled workforce, noncontractual relationships, and other agreements. As an indefinite-lived asset, goodwill is not
amortized but rather is subject to impairment testing on at least an annual basis. The Contura acquisition resulted in the recognition of $109.8 million of
goodwill, which is not expected to be deductible for tax purposes.
Contingent consideration
As part of the transaction, the Company agreed to pay Contura $35 million if Bulkamid sales achieve $50 million in any 12-month period before
December 31, 2024. The preliminary fair value of the estimated contingent consideration was determined by using a binary option-based approach. Inputs
used in the assessment include the Company’s projected revenue rate, an appropriate discount rate, volatility, and risk-free rate. The estimated fair value of
the contingent consideration was preliminarily determined to be $6.8 million. After the March 31, 2021 interim financial statements were issued, the
Company received a final valuation report from a third-party valuation firm relating to the contingent consideration. After considering the results of that
valuation report, the Company estimated the fair value of the contingent consideration to be $7.6 million as of the acquisition date. As a result, the fair
value of the contingent consideration increased by $0.8 million with a corresponding increase to goodwill.
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To the extent that the forecast milestone achievements probabilities changed, future fair value measurement adjustments to the contingent
consideration liability will be recognized in the consolidated statements of comprehensive loss.
Deferred tax liabilities
The Company determined the fair value of the deferred tax liabilities related to the acquisition to be $19.3 million.
Transaction-related costs
Acquisition costs are not included as components of consideration transferred and instead are accounted for as expenses in the period in which the
costs are incurred. The Company incurred $4.4 million of acquisition-related costs in the first quarter of fiscal year 2021.
Pro forma (Unaudited)
The following unaudited pro forma financial information presents the consolidated results of operations of the Company with Contura for the
years ended December 31, 2021 and 2020, as if the acquisition had occurred on January 1, 2020 instead of February 25, 2021 (in thousands, except share
and per share data). Contura’s revenue and net loss for the year ended December 31, 2021 were $24.1 million and $2.8 million, respectively, of which
$22.7 million in revenue and $2.2 million in net income was recognized after the February 25, 2021 acquisition date. Revenue and net income recognized
after the acquisition date were recorded within the Company’s consolidated statements of comprehensive loss. The pro forma information does not
necessarily reflect the results of operations that would have occurred had the entities been a single company during the respective periods.
Net revenue
Net loss
Net loss per share, basic and diluted
Weighted-average shares used to compute basic and diluted net loss per share
Years Ended December 31,
2020
2021
181,643 $
(77,535) $
(1.79) $
43,237,536
122,444
(63,183)
(1.66)
38,077,918
$
$
$
The unaudited pro forma financial information above reflects the following pro forma adjustments:
• An adjustment to decrease net loss for the year ended December 31, 2021 by $4.4 million to eliminate integration and acquisition related costs
incurred by the Company and Contura and a corresponding increase to net loss for the year ended December 31, 2020 by $4.4 million to give
effect to the integration and acquisition of Contura as if it had occurred on January 1, 2020.
• An adjustment to increase net loss for the year ended December 31, 2021 by $1.3 million and a corresponding increase to net loss for the year
ended December 31, 2020 by $7.8 million to reflect amortization of the fair value adjustments for intangible assets as if the assets were acquired
January 1, 2020.
• An adjustment to decrease net loss for the year ended December 31, 2020 by $2.2 million to reflect remeasurement of the fair value adjustments
for deferred tax liabilities as if the liabilities were assumed January 1, 2020.
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Item 9. Changes in and Disagreements with Accountants on Accounting and Financial Disclosure.
None.
Item 9A. Controls and Procedures.
Limitations on effectiveness of controls and procedures
In designing and evaluating our disclosure controls and procedures, management recognizes that any controls and procedures, no matter how well
designed and operated, can provide only reasonable assurance of achieving the desired control objectives. In addition, the design of disclosure controls and
procedures must reflect the fact that there are resource constraints and that management is required to apply judgment in evaluating the benefits of possible
controls and procedures relative to their costs.
Evaluation of disclosure controls and procedures
Our management, with the participation of our Chief Executive Officer and Chief Financial Officer, evaluated, as of December 31, 2022, the end
of the period covered by this Annual Report on Form 10-K, the effectiveness of our disclosure controls and procedures (as defined in Rules 13a-15(e) and
15d-15(e) under the Exchange Act. Based on that evaluation, our Chief Executive Officer and Chief Financial Officer concluded that our disclosure
controls and procedures were not effective as of December 31, 2022 due to the material weaknesses in internal control over financial reporting, as
described below.
Management’s Annual Report on Internal Control Over Financial Reporting
Management is responsible for establishing and maintaining adequate internal control over financial reporting, as defined in Rules 13a-
15(f) and 15d-15(f) of the Exchange Act. Internal control over financial reporting is a process designed to provide reasonable assurance regarding the
reliability of financial reporting and the preparation of financial statements in accordance with GAAP. Because of its inherent limitations, internal control
over financial reporting may not prevent or detect misstatements. Projections of any evaluation of effectiveness to future periods are subject to the risk that
controls may become inadequate because of changes in conditions, or that the degree of compliance with the policies or procedures may deteriorate.
Management has conducted, with the participation of our Principal Executive Officer and our Chief Financial Officer, an assessment, including
testing of the effectiveness, of our internal control over financial reporting as of December 31, 2022. Management’s assessment of internal control over
financial reporting was conducted using the criteria set forth by the Committee of Sponsoring Organizations of the Treadway Commission (COSO) in
Internal Control — Integrated Framework (2013 Framework). Based on its assessment, management has concluded that our internal control over financial
reporting was not effective as of December 31, 2022 due to material weaknesses in our internal control over financial reporting described below.
A material weakness is a deficiency, or a combination of deficiencies, in internal control over financial reporting, such that there is a reasonable
possibility that a material misstatement of our annual or interim financial statements will not be prevented or detected on a timely basis.
Management’s assessment of the Company’s internal control over financial reporting as of December 31, 2022 determined that the following
material weaknesses exist:
• We did not maintain appropriately designed controls relating to the determination of the fair value of contingent consideration liability related to
business combination.
• We did not maintain appropriately designed information technology general controls in the areas of user access and segregation of duties related to
certain information technology systems that support the Company’s financial reporting process. Additionally, certain manual controls that are
dependent upon the information derived from the information technology systems are also determined to be ineffective.
These control deficiencies create a reasonable possibility that a material misstatement to the consolidated financial statements will not be
prevented or detected on a timely basis, and therefore, we concluded that the
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deficiencies represent material weaknesses in our internal control over financial reporting, and our internal control over financial reporting was not
effective as of December 31, 2022.
Notwithstanding such material weaknesses in internal control over financial reporting, our management, including our Principal Executive Officer
and our Chief Financial Officer, has concluded that our consolidated financial statements present fairly, in all material respects, our financial position,
results of our operations and our cash flows for the periods presented in this Form 10-K, in conformity with GAAP.
BDO USA, LLP, an independent registered public accounting firm, who audited the consolidated financial statements included in this annual
report, has expressed an adverse opinion on the operating effectiveness of the Company’s internal control over financial reporting as of December 31, 2022.
BDO USA, LLP’s report appears below.
Remediation Plan
We have identified steps as further described below, to remediate the material weaknesses described in this Item 9A and to enhance our overall
control environment. We are committed to ensuring that our internal controls over financial reporting are designed and operating effectively. Our
remediation process includes, but is not limited to:
•
Conducting a comprehensive review and assessment of internal controls over financial reporting to include the design of general information
technology controls in the area of user access provisioning and monitoring controls to enforce appropriate system access and segregation of duties
for systems supporting the Company’s internal controls processes and financial reporting;
• Designing and implementing controls that address the completeness and accuracy of underlying data used in the performance of certain manual
controls over accounting transactions;
•
•
•
Enhancing the design of controls, including the precision of the management review controls relating to key methodologies, assumptions and
inputs used in the determination of the fair value of contingent consideration liability;
Implementing a valuation review checklist that includes specific review attributes to ensure sufficient evidence of an effective review is
documented and maintained to support management’s conclusions; and
Expanding personnel with appropriate experience to devote sufficient time and resources to our internal controls over fair value measurements.
We believe that these actions will remediate the material weaknesses. The weaknesses will not be considered remediated, however, until the
applicable controls operate and management has concluded, through testing, that these controls are operating effectively.
As we continue to evaluate and test the remediation plan outlined above, we may also identify additional measures to address the material
weaknesses or modify certain of the remediation procedures described above. Management, with the oversight of the Audit Committee, will continue to
take steps necessary to remedy the material weaknesses to reinforce the overall design and capability of our control environment.
Changes in internal control over financial reporting
There were no changes in our internal control over financial reporting (as defined in Rules 13a-15(f) and 15d-15(f) under the Exchange Act)
during the most recent fiscal quarter covered by this Annual Report on Form 10-K that have materially affected, or are reasonably likely to materially
affect, our internal control over financial reporting.
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Report of Independent Registered Public Accounting Firm
Shareholders and Board of Directors
Axonics, Inc.
Irvine, California
Opinion on Internal Control over Financial Reporting
We have audited Axonics, Inc.’s (the “Company’s”) internal control over financial reporting as of December 31, 2022, based on criteria established in
Internal Control – Integrated Framework (2013) issued by the Committee of Sponsoring Organizations of the Treadway Commission (the “COSO
criteria”). In our opinion, the Company did not maintain, in all material respects, effective internal control over financial reporting as of December 31,
2022, based on the COSO criteria.
We do not express an opinion or any other form of assurance on management’s statements referring to any corrective actions taken by the Company after
the date of management’s assessment.
We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States) (“PCAOB”), the consolidated
balance sheets of the Company as of December 31, 2022 and 2021, the related consolidated statements of comprehensive loss, stockholders’ equity, and
cash flows for each of the three years in the period ended December 31, 2022, and the related notes (collectively referred to as the “consolidated financial
statements”) and our report dated March 1, 2023 expressed an unqualified opinion thereon.
Basis for Opinion
The Company’s management is responsible for maintaining effective internal control over financial reporting and for its assessment of the effectiveness of
internal control over financial reporting, included in the accompanying Item 9A, Management’s Annual Report on Internal Control Over Financial
Reporting. Our responsibility is to express an opinion on the Company’s internal control over financial reporting based on our audit. We are a public
accounting firm registered with the PCAOB and are required to be independent with respect to the Company in accordance with U.S. federal securities
laws and the applicable rules and regulations of the Securities and Exchange Commission and the PCAOB.
We conducted our audit of internal control over financial reporting in accordance with the standards of the PCAOB. Those standards require that we plan
and perform the audit to obtain reasonable assurance about whether effective internal control over financial reporting was maintained in all material
respects. Our audit included obtaining an understanding of internal control over financial reporting, assessing the risk that a material weakness exists, and
testing and evaluating the design and operating effectiveness of internal control based on the assessed risk. Our audit also included performing such other
procedures as we considered necessary in the circumstances. We believe that our audit provides a reasonable basis for our opinion.
A material weakness is a deficiency, or a combination of deficiencies, in internal control over financial reporting, such that there is a reasonable possibility
that a material misstatement of the company’s annual or interim financial statements will not be prevented or detected on a timely basis. Material
weaknesses regarding management’s failure to design and implement controls over (i) the determination of the fair value of contingent consideration
liability in a business combination and (ii) the design of information technology general controls related to user access and segregation of duties and certain
manual controls that are dependent upon the information derived from such information technology systems have been identified and described in
management’s assessment. These material weaknesses were considered in determining the nature, timing, and extent of audit tests applied in our audit of
the 2022 consolidated financial statements, and this report does not affect our report dated March 1, 2023 on those consolidated financial statements.
Definition and Limitations of Internal Control over Financial Reporting
A company’s internal control over financial reporting is a process designed to provide reasonable assurance regarding the reliability of financial reporting
and the preparation of financial statements for external purposes in accordance with generally accepted accounting principles. A company’s internal control
over financial reporting includes those policies and procedures that (1) pertain to the maintenance of records that, in reasonable detail, accurately and fairly
reflect the transactions and dispositions of the assets of the company; (2) provide reasonable assurance that transactions are recorded as necessary to permit
preparation of financial statements in accordance with generally accepted accounting principles, and that receipts and expenditures of the company are
being made
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only in accordance with authorizations of management and directors of the company; and (3) provide reasonable assurance regarding prevention or timely
detection of unauthorized acquisition, use, or disposition of the company’s assets that could have a material effect on the financial statements.
Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluation of
effectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of
compliance with the policies or procedures may deteriorate.
/s/ BDO USA, LLP
Costa Mesa, California
March 1, 2023
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Item 9B. Other Information.
None.
Item 9C. Disclosure Regarding Foreign Jurisdictions that Prevent Inspections.
Not applicable.
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Table of Contents
Item 10. Directors, Executive Officers and Corporate Governance.
PART III
The information required by this Item 10 is incorporated herein by reference to our definitive proxy statement to be filed within 120 days of
December 31, 2022 and delivered to stockholders in connection with our 2023 annual meeting of stockholders.
Item 11. Executive Compensation.
The information required by this Item 11 is incorporated herein by reference to our definitive proxy statement to be filed within 120 days of
December 31, 2022 and delivered to stockholders in connection with our 2023 annual meeting of stockholders.
Item 12. Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters.
The information required by this Item 12 is incorporated herein by reference to our definitive proxy statement to be filed within 120 days of
December 31, 2022 and delivered to stockholders in connection with our 2023 annual meeting of stockholders.
Item 13. Certain Relationships and Related Transactions, and Director Independence.
The information required by this Item 13 is incorporated herein by reference to our definitive proxy statement to be filed within 120 days of
December 31, 2022 and delivered to stockholders in connection with our 2023 annual meeting of stockholders.
Item 14. Principal Accounting Fees and Services.
The information required by this Item 14 is incorporated herein by reference to our definitive proxy statement to be filed within 120 days of
December 31, 2022 and delivered to stockholders in connection with our 2023 annual meeting of stockholders.
Item 15. Exhibits and Financial Statement Schedules.
(a) The following documents are filed as part of this Annual Report on Form 10-K:
1. Consolidated Financial Statements:
The following financial statements are filed as a part of this Annual Report on Form 10-K:
PART IV
Report of Independent Registered Public Accounting Firm (BDO USA, LLP; Costa Mesa, California; PCAOB ID#243)
Consolidated Balance Sheets
Consolidated Statements of Comprehensive Loss
Consolidated Statements of Stockholders’ Equity
Consolidated Statements of Cash Flows
Notes to Consolidated Financial Statements
2. Financial Statement Schedules:
All schedules are omitted because they are not applicable or the amounts are immaterial or the required information is presented in the consolidated
financial statements and notes thereto in Part II, Item 8 above.
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3. Exhibits:
Exhibit Number
Exhibit Title
Form
Incorporated by Reference
File No.
Exhibit
Filing Date
Filed Herewith (X)
EXHIBIT INDEX
3.1
3.2
3.3
4.1
4.2
10.1+
10.2+
10.3+
10.4+
10.5
10.6
10.7
10.8
10.9
10.10
Amended and Restated Certificate of
Incorporation.
Certificate of Amendment of Amended
and Restated Certificate of Incorporation
of Registrant filed April 1, 2021.
Amended and Restated Bylaws.
Specimen certificate evidencing shares of
common stock of the Registrant.
Description of Securities.
2018 Omnibus Incentive Plan.
Form of Option Award Agreement under
2018 Omnibus Incentive Plan.
Form of Restricted Shares Award
Agreement under 2018 Omnibus
Incentive Plan.
Form of RSU Award Agreement under
2018 Omnibus Incentive Plan.
Loan and Security Agreement, dated
February 6, 2018, by and between Silicon
Valley Bank.
Amendment to Loan and Security
Agreement, dated October 22, 2018, by
and between Silicon Valley Bank and the
Registrant.
Second Amendment to Loan and Security
Agreement, dated as of December 30,
2019, by and between Axonics
Modulation Technologies, Inc. and
Silicon Valley Bank.
Loan and Security Agreement, dated as of
February 25, 2021, by and among Silicon
Valley Bank and Axonics, Inc.
Lease, dated November 30, 2017, by and
between The Irvine Company LLC and
the Registrant.
First Amendment to Lease, dated
April 12, 2018, by and between The
Irvine Company LLC and the Registrant.
8-K
001-38721
8-K
8-K
S-1
10-K
S-1/A
001-38721
001-38721
333-227732
001-38721
333-227732
S-1/A
333-227732
S-1/A
333-227732
S-1/A
333-227732
3.1
3.1
3.2
4.1
4.4
10.8
10.9
10.10
10.11
11/5/2018
4/1/2021
11/5/2018
10/5/2018
3/1/2021
10/22/2018
10/22/2018
10/22/2018
10/22/2018
S-1
333-227732
10.16
10/5/2018
S-1/A
333-227732
10.31
10/22/2018
8-K
001-38721
1.1
1/2/2020
10-Q
001-38721
10.3
5/7/2021
S-1
333-227732
10.13
10/5/2018
S-1
333-227732
10.14
10/5/2018
111
Table of Contents
10.11
10.12
10.13+
10.14+
10.15+
10.16+
10.17+
10.18
10.19
10.20
10.21
10.22*
Second Amendment to Lease, dated
July 11, 2018, by and between The Irvine
Company LLC and the Registrant.
Third Amendment to Lease, dated June
28, 2019, by and between The Irvine
Company LLC and Axonics Modulation
Technologies, Inc.
Executive Employment Agreement, dated
June 5, 2019, by and between Raymond
W. Cohen and the Registrant.
Executive Employment Agreement, dated
June 5, 2019, by and between Dan L.
Dearen and the Registrant.
Executive Employment Agreement, dated
June 5, 2019, by and between Rinda Sama
and the Registrant.
Amended and Restated Executive
Employment Agreement, dated June 6,
2019, by and between John Woock, Ph.D.
and the Registrant
Amended and Restated Executive
Employment Agreement, dated June 5,
2019, by and between Alfred Ford Jr. and
the Registrant
License Agreement, dated October 1,
2013, by and between the Alfred E. Mann
Foundation for Scientific Research and
the Registrant.
First Amendment to License Agreement,
dated February 19, 2014, by and between
the Alfred E. Mann Foundation for
Scientific Research and the Registrant.
Second Amendment to License
Agreement, dated February 25, 2014, by
and between the Alfred E. Mann
Foundation for Scientific Research and
the Registrant.
Side Letter, dated October 1, 2013, by and
between the Alfred E. Mann Foundation
for Scientific Research and the Registrant.
Form of Indemnification Agreement by
and between the Registrant and its
directors and officers.
S-1
333-227732
10.15
10/5/2018
8-K
001-38721
10.1
7/12/2019
10-Q
001-38721
10.2
8/5/2019
10-Q
001-38721
10.3
8/5/2019
10-Q
001-38721
10.4
8/5/2019
S-1
333-227732
10.1
10/5/2018
S-1
333-227732
10.2
10/5/2018
S-1
333-227732
10.3
10/5/2018
S-1
333-227732
10.4
10/5/2018
S-1/A
333-227732
10.12
10/22/2018
112
X
X
Table of Contents
10.23*
10.24
21.1
23.1
24.1
31.1
31.2
32.1#
32.2#
101.INS**
101.SCH**
101.CAL**
101.DEF**
101.LAB**
101.PRE**
Agreement, dated February 25, 2021, by
and among Axonics, Inc., Axonics
Modulation Technologies, U.K. Limited
and Contura Holdings.
Exclusive Manufacturing and Supply
Agreement, dated February 25, 2021, by
and between Contura International A/S
and Contura Limited.
List of Subsidiaries.
Consent of Independent Registered Public
Accounting Firm.
Power of Attorney (see page 117)
Certification of Principal Executive
Officer pursuant to Rule 13a-14(a) or
Rule 15d-14(a) of the Securities
Exchange Act of 1934, as amended.
Certification of Principal Financial
Officer pursuant to Rule 13a-14(a) or
Rule 15d-14(a) of the Securities
Exchange Act of 1934, as amended.
Certifications of Principal Executive
Officer pursuant to 18 U.S.C. Section
1350, as adopted pursuant to Section 906
of the Sarbanes-Oxley Act of 2002.
Certifications of Principal Financial
Officer pursuant to 18 U.S.C. Section
1350, as adopted pursuant to Section 906
of the Sarbanes-Oxley Act of 2002.
XBRL Instance Document.
XBRL Taxonomy Extension Schema
Document.
XBRL Taxonomy Extension Calculation
Linkbase Document.
XBRL Taxonomy Extension Definition
Linkbase Document.
XBRL Taxonomy Extension Label
Linkbase Document.
XBRL Taxonomy Extension Presentation
Linkbase Document.
10-Q
001-38721
10.1
5/7/2021
10-Q
001-38721
10.2
5/7/2021
113
X
X
X
X
X
X
X
X
X
X
X
X
X
Table of Contents
Indicates management contract or
compensatory plan.
+
The information in Exhibits 32.1 and
32.2 shall not be deemed “filed” for
purposes of Section 18 of the
Exchange Act, or otherwise subject to
the liabilities of that section, nor shall
it be deemed incorporated by
reference in any filing under the
Securities Act or the Exchange Act
(including this Annual Report on
Form 10-K), unless the Registrant
specifically incorporates the foregoing
information into those documents by
reference.
Portions of this exhibit have been
omitted as the Company has
determined that (i) the omitted
information is not material and (ii) the
omitted information would likely
cause competitive harm if publicly
disclosed.
In accordance with Rule 402 of
Regulation S-T, this interactive data
file is deemed not filed or part of this
Annual Report on Form 10-K for
purposes of Sections 11 or 12 of the
Securities Act or Section 18 of the
Exchange Act and otherwise is not
subject to liability under these
sections.
#
*
**
114
Table of Contents
Item 16. Form 10-K Summary.
None.
115
Table of Contents
Pursuant to the requirements of Section 13 or 15(d) of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its
behalf by the undersigned, thereunto duly authorized.
SIGNATURES
Date: March 1, 2023
AXONICS, INC.
By:
/s/ Raymond W. Cohen
Raymond W. Cohen
Chief Executive Officer and Director
116
Table of Contents
POWER OF ATTORNEY
Each person whose signature appears below constitutes and appoints each of Raymond W. Cohen and Dan L. Dearen as his attorney-in-fact, with full
power of substitution, for him in any and all capacities, to sign any amendments to this Form 10-K, and to file the same, with all exhibits thereto and other
documents in connection therewith, with the Securities and Exchange Commission, hereby ratifying and confirming all that each attorney-in-fact, or his
substitute, may do or case to be done by virtue hereof.
Pursuant to the requirements of the Securities Exchange Act of 1934, the report has been signed below by the following persons on behalf of the registrant
and in the capacities and on the dates indicated.
Date: March 1, 2023
Date: March 1, 2023
Date: March 1, 2023
Date: March 1, 2023
Date: March 1, 2023
Date: March 1, 2023
Date: March 1, 2023
Date: March 1, 2023
/s/ Raymond W. Cohen
Raymond W. Cohen
Chief Executive Officer and Director
(Principal Executive Officer)
/s/ Dan L. Dearen
Dan L. Dearen
President and Chief Financial Officer
(Principal Financial and Accounting Officer)
/s/ Michael H. Carrel
Michael H. Carrel
Chairman of the Board and Director
/s/ Jane E. Kiernan
Jane E. Kiernan
Director
/s/ Robert E. McNamara
Robert E. McNamara
Director
/s/ Nancy Snyderman, M.D., FACS
Nancy Snyderman, M.D., FACS
Director
/s/ David M. Demski
David M. Demski
Director
/s/ Esteban López
Esteban López, M.D.
Director
By:
By:
By:
By:
By:
By:
By:
By:
117
AMENDED AND RESTATED EXECUTIVE EMPLOYMENT AGREEMENT
Exhibit 10.16
This Amended and Restated Executive Employment Agreement (this “Agreement”) is dated as of June 6, 2019 by and between
Axonics Modulation Technologies, Inc., a Delaware corporation (the “Company”), and John Woock, Ph.D. (“Executive”).
WHEREAS, Executive currently serves as Chief Marketing Officer of the Company pursuant to an Executive Employment
Agreement dated July 24, 2018 and ending on December 31, 2021 (the “Original Employment Agreement”); and
WHEREAS, the Company and Executive desire to amend and restate the Original Employment Agreement in its entirety in
accordance with the terms of this Agreement.
NOW, THEREFORE, in consideration of the premises and agreements contained herein, and for other good and valuable
consideration, the receipt and sufficiency of which are hereby acknowledged, the parties agree as follows:
1. DEFINED TERMS. Exhibit A to this Agreement sets forth defined terms for purposes of this Agreement.
2. EMPLOYMENT/TERM. The Company hereby employs Executive to perform the duties and responsibilities set forth below under
Section 3 of this Agreement, and Executive hereby accepts such employment, in each case on the terms and conditions set forth in
this Agreement. This Agreement shall commence on the Effective Date and remain in effect for five (5) years, unless earlier
terminated pursuant to Section 5 of this Agreement (the “Term”).
3. POSITION AND DUTIES.
a. Description of Executive’s Position, Duties, Authorities, and Responsibilities. Executive shall serve as the Chief Marketing
Officer of the Company. In such capacity, Executive shall (i) report to the Chief Executive Officer, (ii) devote Executive’s
full professional time and attention, best efforts, energy and skills to the services required of Executive as an employee of the
Company, except for paid time off taken in accordance with the Company’s policies and practices, and subject to the
Company’s policies pertaining to reasonable periods of absence due to sickness, personal injury or other disability; (iii) use
Executive’s best efforts to promote the interests of the Company; (iv) comply with all
1
applicable governmental laws, rules and regulations and with all of the Company’s policies, rules and regulations applicable
to employees of the Company; (v) participate in, and comply with all Company directives regarding, workplace
investigations; and (vi) discharge Executive’s responsibilities in a diligent and faithful manner, consistent with sound
business practices and in accordance with the Board’s directives.
b. Outside Boards. Executive shall obtain the written consent of the Board prior to serving on corporate, civic or charitable
boards or committees. This Section 3.b shall not be construed as preventing Executive from serving on the corporate, civic or
charitable boards or committees on which Executive serves as of the Effective Date and which have been previously
disclosed to the Board in writing; provided that in no event shall any such service or business activity require the provision
of substantial services by Executive to the operations or the affairs of such businesses or enterprises such that the provision
thereof would interfere in any respect with the performance of Executive’s duties hereunder or cause a conflict of interest to
the interests of the Company.
4. COMPENSATION AND BENEFITS.
a. Base Salary. As of the Effective Date, Executive’s Base Salary shall be three hundred thousand dollars ($300,000) per year
payable in periodic installments in accordance with the Company’s regular payroll practices as in effect from time to time.
The Board or a duly authorized committee thereof will review the Base Salary on an annual basis and may increase the Base
Salary from time to time based on merit or such other considerations as the Board or a duly authorized committee thereof
may deem appropriate.
b. Bonus. Executive shall be eligible to receive an annual cash bonus in an amount up to thirty percent (30%) of Executive’s
Base Salary for the calendar year for which the annual cash bonus is being paid, as determined in the discretion of the Board
or a duly authorized committee thereof, based on the performance of the Company and Executive relative to performance
objectives or other metrics as the Board or a duly authorized committee thereof may deem appropriate. The Board shall
establish performance objectives or other metrics within 90 days after the beginning of each new calendar year.
c. Benefits and Vacation. Executive shall be eligible to participate in and receive the benefits under any deferred compensation
plan, health, life, accident and disability insurance plans
2
or programs, and any other employee benefit or fringe benefit plans or arrangements that the Company makes available
generally to other senior executives of the Company, pursuant to the provisions of such plans, programs or arrangements as
in effect from time to time. Executive shall be entitled to four week’s paid vacation and additional sick days in accordance
with the policies of the Company for its employees generally, as in effect from time to time.
d. Equity Incentive Compensation. Executive shall be eligible to receive grants, at the discretion of the Board or a duly
authorized committee thereof, under any long-term equity- based incentive compensation plans established or maintained by
the Company for its senior executive officers, in each case subject to the terms and conditions of the applicable plans and
award documents with respect to such grants.
e. Expenses. The Company shall pay or reimburse Executive for all reasonable, ordinary and necessary business expenses
incurred or paid by Executive during the Term in the performance of Executive’s services under this Agreement in
accordance with the applicable policies and procedures of the Company as in effect from time to time, upon the presentation
of proper expense statements or such other supporting documentation as the Company may reasonably require.
5. TERMINATION OF EMPLOYMENT.
a. General. Executive’s employment may be terminated by either party at any time and for any reason; and upon termination of
Executive’s employment, the Term shall end.
b. Resignation without Good Reason. Executive may resign from employment with the Company without Good Reason by
providing the Company with at least 60 days’ advance written notice. During the Resignation Notice Period, the Company,
in its sole discretion, may elect to accelerate Executive’s date of termination of employment, it being understood that any
such termination shall still be treated as a voluntary resignation without Good Reason for purposes of this Agreement. Even
if Executive’s date of termination is accelerated, Executive shall be paid Executive’s Base Salary, and shall receive Benefits
capable of being provided to persons who are not actively employed by the Company, as if Executive had worked through
the end of the Resignation Notice Period. The Company reserves the right to require Executive not to be in the offices of the
Company or any of its
3
affiliates and/or not to undertake all or any of Executive’s duties and/or not to contact clients, colleagues or advisors of the
Company or any of its affiliates during all or part of the Resignation Notice Period. During the Resignation Notice Period,
Executive’s terms and conditions of service and duties of loyalty and confidentiality to the Company shall remain in full
force and effect and, during any such Resignation Notice Period, Executive shall continue to perform as an employee in
compliance with the terms of this Agreement and all other agreements applicable to Executive with respect to Executive’s
service with the Company or any of its affiliates.
c. Death. Executive’s employment hereunder shall terminate automatically on the date of Executive’s death.
d. Disability. At the option of the Company, Executive’s employment hereunder may be terminated immediately upon
Disability.
e. Termination for Cause. Notwithstanding any other provision of this Agreement, the Company may, at any time, immediately
terminate Executive’s employment for Cause. The Company’s lack of immediate action with respect to conduct of Executive
that would constitute Cause hereunder shall not preclude the Company from taking later action on such act or taking action
with respect to another such act committed by Executive.
f. Termination Without Cause. The Company may, at any time, immediately terminate Executive’s employment without Cause.
6. COMPENSATION UPON TERMINATION (OTHER THAN A CHANGE IN CONTROL TERMINATION). Following any
termination of Executive’s employment, the obligations of the Company to pay or provide Executive with compensation and benefits
under Section 4 shall immediately cease, and the Company shall have no further obligations to Executive under this Agreement,
except to provide (i) the Accrued Obligations, (ii) any additional amounts specifically provided by this Section 6, subject to the
applicable terms and conditions of this Section 6, and (iii) any other amounts otherwise required by law.
a. Death or Disability. If, during the Term, Executive’s employment is terminated (x) by reason of Executive’s death or (y) by
the Company for Disability, in addition to the Accrued Obligations, Executive shall receive the following compensation:
4
i.
The Company shall pay to Executive (or to Executive’s estate or designated beneficiary in the event of Executive’s
death) a lump sum amount equal to (A) one (1) year of Base Salary in effect as of the Termination Date, plus (B) the
annual bonus earned based on performance for the year immediately preceding the year in which the Termination
Date occurs, to the extent such bonus had not been paid as of the Termination Date, plus (C) if the Termination Date
occurs during the second, third or fourth quarter of a year, the Pro-Rata Bonus for that year. Such payment shall be
made in a single cash payment on the Cash Severance Commencement Date, provided that on or before the Cash
Severance Commencement Date, Executive has executed, and delivered a general waiver and release agreement in
the form of Exhibit B, attached, or in a form and with substance satisfactory to the Company, that is no longer
subject to revocation. If Executive is unable to execute and deliver such waiver and release agreement due to death
or Disability, then the waiver and release agreement shall be executed and delivered by an authorized agent or
representative of Executive and/or Executive’s estate.
ii.
As to any outstanding, unvested Equity Incentive Compensation awards on the Termination Date that are not
Performance-Based Awards, except to the extent that the applicable award agreement or equity compensation plan
provides for better treatment and notwithstanding the terms of any applicable award agreements entered into after the
Effective Date (unless such award agreements expressly reference this Agreement), Executive shall immediately vest
in such award. For any such awards that are Performance-Based Awards, vesting shall be based on the terms of the
applicable equity compensation plan and award agreement in accordance with Section 6.d. Vested stock options shall
remain exercisable during the periods provided in the applicable plan and award agreement.
b. For Cause or Without Good Reason. If, during the Term, Executive’s employment is terminated (i) by the Company for
Cause or (ii) by Executive for any reason other than for Good Reason, the Company shall pay to Executive the Accrued
Obligations.
c. Without Cause or for Good Reason (Other than a Change in Control Termination). If, during the Term, Executive’s
employment with the Company terminates by reason of a
5
Qualifying Termination (other than a Change in Control Termination), in addition to the Accrued Obligations, Executive
shall receive the following compensation:
i.
Executive shall receive cash severance in an amount equal to nine (9) months of Base Salary as in effect on the
Termination Date. Such payment shall be made in a single cash payment on the Cash Severance Commencement
Date.
ii.
Executive shall be paid the annual bonus earned based on performance for the year immediately preceding the year
in which the Termination Date occurs, to the extent such bonus had not been paid as of the Termination Date. Such
bonus shall be paid at the same time bonuses are paid to other employees.
iii.
If the Termination Date occurs during the second, third or fourth quarter of a year, Executive shall be paid the Pro-
Rata Bonus for that year, made in a single cash payment on the Cash Severance Commencement Date.
iv.
Executive shall be paid an amount equal to twelve (12) months of COBRA premiums based on the terms of
Company’s group health plan and Executive’s coverage under such plan as of the Termination Date (regardless of
any COBRA election actually made by Executive or the actual COBRA coverage period under the Company’s group
health plan), payable in a single cash payment on the Cash Severance Commencement Date.
v.
As to any outstanding, unvested Equity Incentive Compensation awards on the Termination Date, for any such
awards that are Performance-Based Awards, the award shall vest at the end of the applicable performance period
based on actual performance results and prorated for the portion of the performance period worked through the
Termination Date.
All payments under clauses (i) - (v) of this Section 6.c. are conditioned on (A) Executive, on or before the Cash Severance
Commencement Date, having executed and delivered a general waiver and release agreement in the form of Exhibit B,
attached, or in a form and with substance satisfactory to the Company, that is no longer subject to revocation, and (B)
Executive’s compliance with all applicable post-employment covenants with the Company, including those set forth in
Section 8 of this Agreement.
6
d. Equity Incentive Compensation. Except as otherwise expressly provided herein, upon termination of Executive’s
employment during the Term, any outstanding Equity Incentive Compensation awards shall be forfeited or vest in
accordance with the terms of the applicable plan and award agreement, and shall be subject to such other terms and
conditions of such plan and award agreement that may apply as a result of such termination.
e. Benefits. Notwithstanding anything in this Section 6 to the contrary, the Benefits to which Executive is entitled upon or by
reason of the termination of Executive’s employment with the Company shall be subject to, and shall be governed by, the
terms and conditions of the applicable plans, programs and arrangements maintained by the Company with respect to such
Benefits. Nothing in this Agreement shall be construed to be a waiver by the Executive of any benefits accrued for or due to
the Executive under any employee benefit plan (as such term is defined in the Employee Retirement Income Security Act of
1974, as amended) maintained by the Company, if any, except that the Executive shall not be entitled to any severance
benefits pursuant to any severance plan or program of the Company other than as provided herein.
f. D&O Insurance, and Indemnification. Through at least the sixth anniversary of the Termination Date, the Company shall
maintain coverage for the Executive as a named insured on all directors’ and officers’ insurance maintained by the Company
for the benefit of its directors and officers on at least the same basis as all other covered individuals and provide the
Executive with at least the same corporate indemnification as it provides to other senior executives.
g. Expiration of Term. Notwithstanding anything in this Section 6 to the contrary, the expiration of the Term by itself shall not
entitle Executive to receipt of any payments under this Section 6.
7
7. CHANGE IN CONTROL.
a. Treatment of Equity Incentive Compensation. As to any outstanding, unvested Equity Incentive Compensation awards
immediately before a Change in Control, except to the extent that the applicable award agreement or equity compensation
plan provides for better treatment and notwithstanding the terms of any applicable award agreements entered after the
Effective Date (unless such award agreements expressly reference this Agreement):
i.
For any such awards that are not Performance-Based Awards, (A) the awards shall vest in full immediately upon the
Change in Control, and (B) any vested stock options shall remain exercisable during the periods provided in the
applicable plans and award agreement.
ii.
For any such awards that are Performance-Based Awards, the award shall be fully vested based on the greater of (A)
assumed target performance or (B) performance as determined by the Board immediately before the Change in
Control.
b. Change in Control Severance. If, during the Term, Executive’s employment with the Company terminates by reason of a
Change in Control Termination, in addition to the Accrued Obligations, Executive shall receive the following compensation:
i.
Executive shall receive cash severance in an amount equal to 9 months of Base Salary as in effect on the Termination
Date. Such amount shall be payable in a single cash payment on the Cash Severance Commencement Date.
ii.
Executive shall be paid the annual bonus earned based on performance for the year immediately preceding the year
in which the Termination Date occurs, to the extent such bonus had not been paid as of the Termination Date. Such
bonus shall be paid at the same time bonuses are paid to other employees.
iii.
iv.
Executive shall be paid the Pro-Rata Bonus in a single cash payment on the Cash Severance Commencement Date.
Executive shall be paid an amount equal to 9 months of COBRA premiums based on the terms of Company’s group
health plan and Executive’s coverage under such plan as of the Termination Date (regardless of any COBRA election
actually made by Executive or the actual COBRA coverage period under the Company’s group
8
health plan), payable in a single cash payment on the Cash Severance Commencement Date.
All payments under clauses (i) - (iv) of this Section 7.b. are conditioned on (A) Executive, on or before the Cash Severance
Commencement Date, having executed and delivered a general waiver and release agreement in the form of Exhibit B,
attached, or in a form and with substance satisfactory to the Company, that is no longer subject to revocation, and (B)
Executive’s compliance with all applicable post-employment covenants with the Company, including those set forth in
Section 8 of this Agreement. For avoidance of doubt, if amounts are payable to Executive under this Section 7.b, no amounts
shall be payable to Executive under Section 6.c.
8. NONSOLICITATION COVENANT. Executive agrees that Executive shall not directly or indirectly during the Term and for one
(1) year after termination of Executive’s employment, either alone or through or in conjunction with any other person or entity
employ, solicit, induce, or recruit, any person employed by any member of the Company Group at any time within the one (1) year
period immediately preceding such employment, solicitation, inducement or recruitment.
9. ADJUSTMENTS TO PAYMENTS. Anything in this Agreement to the contrary notwithstanding, in the event it shall be determined
that any payment or distribution by the Company to Executive or for Executive’s benefit (whether paid or payable or distributed or
distributable pursuant to the terms of this Agreement or otherwise) (the “Payments”) would be subject to the excise tax imposed by
Section 4999 (or any successor provisions) of the Code, or any interest or penalty is incurred by Executive with respect to such
excise tax (such excise tax, together with any such interest and penalties, is hereinafter collectively referred to as the “Excise Tax”),
then the Payments shall be reduced (but not below zero) if and to the extent that such reduction would result in Executive retaining a
larger amount, on an after-tax basis (taking into account federal, state and local income taxes and the imposition of the Excise Tax),
than if Executive received all of the Payments. The Company shall reduce or eliminate the Payments, by first reducing or eliminating
the portion of the Payments which are not payable in cash and then by reducing or eliminating cash payments, in each case in reverse
order beginning with payments or benefits which are to be paid the farthest in time from the determination. All
9
determinations required to be made under this Section, including whether and when an adjustment to any Payments is required and, if
applicable, which Payments are to be so adjusted, shall be made by an independent accounting firm selected by the Company from
among the four (4) largest accounting firms in the United States or any nationally recognized financial planning and benefits
consulting company (the “Accounting Firm”) which shall provide detailed supporting calculations both to the Company and to
Executive within fifteen (15) business days of the receipt of notice from Executive that there has been a Payment, or such earlier time
as is requested by the Company. In the event that the Accounting Firm is serving as accountant or auditor for the individual, entity or
group effecting the Change in Control, Executive shall appoint another nationally recognized accounting firm to make the
determinations required hereunder (which accounting firm shall then be referred to as the Accounting Firm hereunder). All fees and
expenses of the Accounting Firm shall be borne solely by the Company. If the Accounting Firm determines that no Excise Tax is
payable by Executive, it shall furnish Executive with a written opinion that failure to report the Excise Tax on Executive's applicable
federal income tax return would not result in the imposition of a negligence or similar penalty. Any determination by the Accounting
Firm shall be binding upon the Company and Executive.
10. COOPERATION. Upon the receipt of reasonable notice from the Company (including outside counsel), Executive agrees that while
employed by the Company and thereafter, Executive will respond and provide information with regard to matters in which Executive
has knowledge as a result of Executive’s employment with the Company, and will provide reasonable assistance to the Company, its
affiliates and their respective representatives in defense of all claims that may be made against the Company or its affiliates, and will
assist the Company and its affiliates in the prosecution of all claims that may be made by the Company or its affiliates, to the extent
that such claims may relate to the period of Executive’s employment with the Company. Executive agrees to promptly inform the
Company if Executive becomes aware of any lawsuit involving such claims that may be filed or threatened against the Company or
its affiliates. Executive also agrees to promptly inform the Company (to the extent that Executive is legally permitted to do so) if
Executive is asked to assist in any investigation of the Company or its affiliates (or their actions), regardless of whether a lawsuit or
other proceeding has then been filed against the Company or its affiliates with respect to such investigation, and shall not provide
such assistance unless legally
10
required. Upon presentation of appropriate documentation, the Company shall pay or reimburse Executive for all reasonable out-of-
pocket travel, duplicating or telephonic expenses incurred by Executive in complying with this Section 10. For the first five hours of
cooperation in any calendar month during the period of cooperation, Executive shall provide the specified cooperation services
without hourly reimbursement. For each hour of cooperation or part thereof after five hours, in any calendar month, Company shall
reimburse Executive at the hourly rate determined by this fraction: (final Base Salary / 2,080 hours).
11. ARBITRATION. The parties hereby agree to submit all disputes, claims and controversies (“Claims”) between the parties or related
to or arising out of their employment relationship by and between the Company and Executive to final, binding arbitration to the
fullest extent permitted by law. The Federal Arbitration Act., 9 U.S.C. § 1 et seq., shall govern the interpretation and enforcement of
this Section 11. The court and not the arbitrator will determine matters of enforceability of this Section 11.
a. Statute of Limitations. The statutory limitations period applicable to a Claim asserted in a civil action shall apply to any such
Claim asserted in any arbitration proceeding under this Section 11. Arbitration is commenced for limitations purposes by
submitting the matter to the arbitral forum.
b.
Individual Basis. All Claims that are subject to arbitration under this Section 11 must and will take place on an individual
basis only.
c. Venue. Binding arbitration under this Section 11 shall be conducted in California unless required by law to be conducted
elsewhere, in which case it shall be conducted where required by law.
d. Applicable Rules. The arbitration proceeding, including discovery, shall be conducted in accordance with the Federal
Arbitration Act, the JAMS Policy on Employment Arbitration Minimum Standards and the JAMS Employment Arbitration
Rules and Procedures then in effect (the “JAMS Rules”). Executive understands that if Executive wishes to receive a copy of
the JAMS Rules currently in effect, Executive may inform the Company in writing, and the Company will provide them to
Executive before Executive executes this Agreement. Executive also understand that JAMS Rules are available online at
http://www.jamsadr.com/rules-employment-arbitration/.
11
e. Arbitrator Selection. The arbitration shall be conducted before a neutral arbitrator selected by all parties in accordance with
JAMS Rules.
f. Cost Allocation. If required by applicable law, the Company shall pay all additional costs peculiar to the arbitration to the
extent such costs would not otherwise be incurred in a court proceeding (for instance, the Company shall pay the arbitrator’s
fees, and the JAMS administration and filing fees, to the extent such fees exceed court filing fees).
g. Attorneys’ Fees and Costs. Each party shall pay such party’s own costs and attorneys’ fees except that the arbitrator shall
award costs and attorneys’ fees to the prevailing party.
h. Written Decision. The arbitrator shall follow applicable substantive law and, within 30 days after the conclusion of the
arbitration, issue a written opinion setting forth the factual and legal bases for his or her decision.
i. Acknowledgement. EXECUTIVE UNDERSTANDS THAT EXECUTIVE IS GIVING UP EXECUTIVE’S RIGHT TO A
JURY TRIAL BY ENTERING INTO THIS AGREEMENT. EXECUTIVE UNDERSTANDS THAT EXECUTIVE IS
GIVING UP EXECUTIVE’S RIGHT TO COMMENCE OR PARTICIPATE IN A CLASS OR COLLECTIVE ACTION
AND INSTEAD AGREES TO ARBITRATE ANY EMPLOYMENT-RELATED DISPUTE ON AN INDIVIDUAL BASIS
ONLY TO THE MAXIMUM EXTENT PERMITTED BY LAW.
12. CODE SECTION 409A.
a. This Agreement is intended to comply with the requirements of Section 409A of the Internal Revenue Code of 1986, as
amended (“Section 409A”), including the exceptions thereto, and shall be construed and administered in accordance with
such intent. Notwithstanding any other provision of this Agreement, payments provided under this Agreement may only be
made upon an event and in a manner that complies with Section 409A or an applicable exemption. Any payments under this
Agreement that may be excluded from Section 409A either as separation pay due to an involuntary separation from service
or as a short-term deferral shall be excluded from Section 409A to the maximum extent possible. For purposes of Section
409A, each separate payment or installment payment provided under this Agreement shall be treated as a separate payment.
Any
12
payments to be made under this Agreement in connection with a termination of employment shall only be made if such
termination of employment constitutes a “separation from service” under Section 409A. Notwithstanding the foregoing, the
Company makes no representations that the payments and benefits provided under this Agreement comply with Section
409A and in no event shall the Company be liable for all or any portion of any taxes, penalties, interest or other expenses that
may be incurred by Executive on account of non-compliance with Section 409A.
b. Notwithstanding any other provision of this Agreement, if at the time of Executive’s termination of employment, Executive
is a “specified employee,” determined in accordance with Section 409A, any payments and benefits provided under this
Agreement that constitute “nonqualified deferred compensation” subject to Section 409A that are provided to Executive on
account of Executive’s separation from service shall not be paid until the first payroll date to occur following the six-month
anniversary of Executive’s termination date (“Specified Employee Payment Date”). The aggregate amount of any payments
that would otherwise have been made during such six-month period shall be paid in a lump sum on the Specified Employee
Payment Date and thereafter, any remaining payments shall be paid without delay in accordance with their original schedule.
If Executive dies before the Specified Employee Payment Date, any delayed payments shall be paid to Executive’s estate in a
lump sum within one week of Executive’s death.
c. To the extent required by Section 409A, each reimbursement or in-kind benefit provided under this Agreement shall be
provided in accordance with the following: (i) the amount of expenses eligible for reimbursement, or in-kind benefits
provided, during each calendar year cannot affect the expenses eligible for reimbursement, or in-kind benefits to be provided,
in any other calendar year; (ii) any reimbursement of an eligible expense shall be paid to Executive on or before the last day
of the calendar year following the calendar year in which the expense was incurred; and (iii) any right to reimbursements or
in-kind benefits under this Agreement shall not be subject to liquidation or exchange for another benefit. Any tax gross-up
payments provided under this Agreement shall be paid to Executive on or before December 31 of the calendar year
immediately following the calendar year in which Executive remits the related taxes.
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d. Whenever in this Agreement a payment or benefit is conditioned on Executive’s execution of a release of claims, such
release must be executed, and all revocation periods shall have expired within 60 days after the Termination Date; failing
which such payment or benefit shall be forfeited. If such payment or benefit constitutes “nonqualified deferred
compensation” subject to Section 409A, and if such 60-day period begins in one calendar year and ends in the next calendar
year, the payment or benefit shall not be made or commence before the second such calendar year, even if the release
becomes irrevocable in the first such calendar year.
13. GENERAL PROVISIONS.
a. Notices. All notices, requests, demands, statements, reports and other communications provided for by this Agreement shall
be in writing (email being sufficient) and shall be sent by (i) certified mail, return receipt requested, postage prepaid, (ii)
nationally recognized overnight delivery service, (iii) personal delivery or (iv) email. A notice shall be deemed to be given
(x) if notice is delivered by certified mail or nationally recognized overnight delivery service, on the business day following
the date of its mailing, (y) if such notice is delivered personally, upon delivery, or (z) if such notice is sent by email, upon
sending. Each party may change such party’s address for notices by giving notice in accordance herewith. All notices shall
be addressed and mailed or delivered to the following addresses:
If to the COMPANY:
Attn: Chief Executive Officer
Axonics Modulation Technologies, Inc. 26 Technology Drive
Irvine, CA 92618
If to EXECUTIVE:
John Woock, Ph.D.
c/o Axonics Modulation Technologies, Inc. 26 Technology Drive
Irvine, CA 92618
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b. Entire Agreement. This Agreement constitutes the entire agreement between the parties with respect to the subject matter
hereof and supersedes all prior agreements, representations and understandings (whether written or oral) of the parties with
respect to the subject matter hereof, including the Original Employment Agreement, and any other agreement between
Executive and the Company or any of its affiliates and subsidiaries.
c. Modification and Waiver. No amendment or variation of the terms of this Agreement shall be valid unless made in writing
and signed by Executive and a duly authorized representative of the Company (other than Executive). A waiver of any term
or condition of this Agreement shall not be construed as a general waiver by the Company. If one or more provisions of this
Agreement are held to be illegal or unenforceable under applicable law, such illegal or unenforceable provision(s) shall be
limited or excluded from this Agreement to the minimum extent required so that this Agreement shall otherwise remain in
full force and effect and enforceable in accordance with its terms.
d. Governing Law. This Agreement shall be governed by and construed in accordance with the laws of the State of California,
without giving effect to its conflict of law principles, and any dispute in the meaning, effect or validity of this Agreement
shall be resolved in accordance with the laws of the State of California.
e. Assignment; Binding Effect. This Agreement is fully assignable and transferable by the Company, but any purported
assignment or transfer by Executive is void. It is hereby agreed that Executive’s rights and obligations under this Agreement
are personal and not assignable by Executive. This Agreement shall be binding upon and inure to the benefit of the heirs,
legal representatives, successors and permitted assigns of the parties. EXECUTIVE HAS READ THIS AGREEMENT
CAREFULLY AND UNDERSTANDS AND ACCEPTS THE OBLIGATIONS WHICH IT IMPOSES UPON
EXECUTIVE WITHOUT RESERVATION. NO PROMISES OR REPRESENTATIONS HAVE BEEN MADE TO
EXECUTIVE TO INDUCE EXECUTIVE TO SIGN THIS AGREEMENT. EXECUTIVE SIGNS THIS
AGREEMENT VOLUNTARILY AND FREELY, IN DUPLICATE, WITH THE UNDERSTANDING THAT THE
COMPANY WILL RETAIN ONE
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COUNTERPART AND THE OTHER COUNTERPART WILL BE RETAINED BY EXECUTIVE.
f.
Injunctive Relief. Executive agrees that any breach of this Agreement will cause irreparable harm to the Company for which
damages would not be an adequate remedy, and, therefore, to the fullest extent permitted by applicable law, the Company
will be entitled to injunctive relief with respect thereto in addition to any other remedies and without any requirement to post
bond.
g. Survival. This Agreement shall terminate upon the expiration of the Term; provided that the provisions of Section 1 and
Sections 6 through 13 shall survive termination of this Agreement and termination of Executive’s employment regardless of
the reason for such termination.
h. Withholding. The Company may withhold from any and all amounts payable under this Agreement or otherwise such
federal, state and local taxes as may be required to be withheld pursuant to applicable law.
[Signature page follows]
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In witness whereof, the parties have executed this Agreement as of the date first above written.
COMPANY:
Axonics Modulation Technologies, Inc.
By: /s/ Raymond W. Cohen
Raymond W. Cohen
Chief Executive Officer
EXECUTIVE:
/s/ John Woock, Ph.D.
John Woock, Ph.D.
Signature Page to Amended and Restated Executive Employment Agreement
EXHIBIT A
For purposes of interpreting the Agreement, the following definitions shall apply:
“Accrued Obligations” means, in connection with Executive’s termination of employment with the Company for any reason, (i) any
unpaid Base Salary accrued through the Termination Date, payable as soon as practicable (not more than 30 days) after the Termination Date,
and (ii) any unpaid Benefits accrued through the Termination Date to which Executive is entitled under any plans, programs or arrangements
applicable to terminated employees in which Executive participates, payable in accordance with the terms of such plans, programs or
arrangements.
“Base Salary” means Executive’s annual rate of base salary from the Company as provided in Section 4.a (including any permitted
adjustments to the annual rate of base salary during the Term as provided by Section 4.a).
“Benefits” means the employee benefits provided to Executive by the Company under the provisions of Section 4.c.
“Board” means the Board of Directors of the Company.
“Cash Severance Commencement Date” means the 60th day after the Termination Date.
“Cause” means the occurrence of any of the following by Executive: (i) fraud, misappropriation, embezzlement or acts of similar
dishonesty; (ii) conviction of, or plea of nolo contendere to, a felony; (iii) excessive use of alcohol or illegal use of drugs in the workplace;
(iv) gross negligence or intentional or willful misconduct by Executive in the performance of Executive’s duties; (v) breach of Executive’s
duty of loyalty to the Company or diversion or usurpation of corporate opportunities properly belonging to the Company; (vi) the knowing
breach of the Company’s confidentiality agreement to which the Executive is a party to; or (vii) violation of any material provision of this
Agreement or any other material provision of any other agreement between Executive and the Company.
“Change in Control” means a “Change in Control” as defined under the Axonics Modulation Technologies, Inc. 2018 Omnibus
Incentive Plan.
“Change in Control Protected Period” means the period commencing on the date of a Change in Control and ending on first
anniversary of the date of the Change in Control.
“Change in Control Termination” means a Qualifying Termination that occurs during the Change in Control Protected Period.
“Disability” means any physical or mental illness, impairment or incapacity which, in the good faith determination of the Board, has
prevented Executive from performing the essential functions of Executive’s position hereunder for a period of 90 or more consecutive days
(or for shorter periods totaling 120 days) during any period of 12 consecutive months, consistent with applicable law.
“Effective Date” means July 1, 2019, the effective date of this Agreement and the first day of the Term.
“Equity Incentive Compensation” means the equity compensation awards provided to Executive by the Company under Section 4.d.
“Good Reason” means the occurrence of any of the following events, without the express consent of Executive, (i) a material
diminution in Executive’s Base Salary, or (ii) a material diminution in Executive’s position, duties, authorities or responsibilities (other than
temporarily while physically or mentally incapacitated or as required by applicable law). In order for Executive to terminate Executive’s
employment for Good Reason, (x) Executive must furnish written notice to the Company setting forth the facts and circumstances claimed to
provide a basis for such resignation within 30 days following the occurrence of such facts and circumstances, (y) the Company shall have 30
days after its receipt of such written notice to cure such facts and circumstances in all material respects (and if so cured, then Executive shall
not be permitted to resign for Good Reason in respect thereof), and (z) Executive must actually terminate Executive’s employment within 30
days following the expiration of the Company’s cure period set forth above.
“Performance-Based Award” means an option, restricted stock or other Equity Incentive Compensation award that vests based on
performance-based criteria.
“Pro-Rata Bonus” means an amount determined as of Executive’s Termination Date as follows: (i) if Executive’s termination of
employment is due to Executive’s death or Disability or by reason of a Qualifying Termination that is not a Change in Control Termination,
the Pro-Rata Bonus shall equal the actual annual cash bonus earned based on performance through the Termination Date as determined by the
Board, multiplied by the Pro-Rata Fraction, payable in a lump sum at the time specified in Section 6.a or Section 6.c (as applicable); and (ii)
if Executive’s termination of employment is due to a Change in
Control Termination, the Pro-Rata Bonus shall equal the target annual cash bonus for the year in which the Termination Date occurs,
multiplied by the Pro-Rata Fraction, and payable in a lump sum at the time specified in Section 7.b.
“Pro-Rata Fraction” means a fraction, the numerator of which is the number of days in the calendar year through Executive’s
Termination Date and the denominator of which is 365.
“Qualifying Termination” means a termination of Executive’s employment with the Company during the Term either (i) by the
Company other than for Cause, or (ii) by Executive with Good Reason.
“Resignation Notice Period” means the period, not less than 60 days, between the date Executive provides the Company with
written notice of his intent to resign from employment with the Company and the intended effective date of such resignation.
“Termination Date” means the date of Executive’s termination of employment with the Company as determined under this
Agreement.
EXHIBIT B
GENERAL RELEASE
I, ___________ in consideration of and subject to the performance by Axonics Modulation Technologies, Inc. (together with its
subsidiaries and successors, the “Company”), of its obligations under the Amended and Restated Executive Employment Agreement dated as
of ___________, 2019 (the “Agreement”), do hereby release and forever discharge as of the date hereof the Company and its respective
affiliates, subsidiaries and direct or indirect parent entities and all present, former and future directors, officers, agents, representatives,
employees, successors and assigns of the Company and/or its respective affiliates, subsidiaries and direct or indirect parent entities
(collectively, the “Released Parties”) to the extent provided below (this “General Release”). The Released Parties are intended to be third-
party beneficiaries of this General Release, and this General Release may be enforced by each of them in accordance with the terms hereof in
respect of the rights granted to such Released Parties hereunder. Terms used herein but not otherwise defined shall have the meanings given
to them in the Agreement.
1.
I understand that any payments or benefits paid or granted to me under the Agreement represent, in part, consideration for signing
this General Release and are not salary, wages or benefits to which I was already entitled. I understand and agree that I will not receive
certain of the payments and benefits specified in the Agreement unless I execute this General Release and do not revoke this General Release
within the time period permitted hereafter. Such payments and benefits will not be considered compensation for purposes of any employee
benefit plan, program, policy or arrangement maintained or hereafter established by the Company or its affiliates.
2.
Except as provided in paragraphs 4 and 5 below and except for the provisions of the Agreement which expressly survive the
termination of my employment with the Company, I knowingly and voluntarily (for myself, my heirs, executors, administrators and assigns)
release and forever discharge the Company and the other Released Parties from any and all claims, suits, controversies, actions, causes of
action, cross-claims, counter claims, demands, debts, compensatory damages, liquidated damages, punitive or exemplary damages, other
damages, claims for costs and attorneys’ fees, or liabilities of any nature whatsoever in law and in equity, both past and present (through the
date that this General Release becomes effective and enforceable) and whether known or unknown, suspected, or claimed against the
Company or any of the Released Parties which I, my spouse, or any of my heirs, executors, administrators or assigns, may have, which arise
out of or are connected with my employment with, or my separation or
1
termination from, the Company (including, but not limited to, any allegation, claim or violation, arising under: Title VII of the Civil Rights
Act of 1964, as amended; the Civil Rights Act of 1991; the Age Discrimination in Employment Act of 1967, as amended (including the
Older Workers Benefit Protection Act); the Equal Pay Act of 1963, as amended; the Americans with Disabilities Act of 1990; the Americans
with Disabilities Act Amendments Act of 2008; the Family and Medical Leave Act of 1993; the Labor Management Relations Act; the
Worker Adjustment Retraining and Notification Act; the Employee Retirement Income Security Act of 1974; the Sarbanes-Oxley Act of
2002; the California Worker Adjustment Retraining and Notification Act; the California Fair Employment and Housing Act; the California
Labor Code; the California Family Rights Act; the California Industrial Welfare Commission Wage Orders; the California Constitution; the
California Government Code; any applicable Executive Order Programs; the Fair Labor Standards Act; or their state or local counterparts; or
under any other federal, state or local civil or human rights law, or under any other local, state, or federal law, regulation or ordinance, as well
as any amendments to any of the foregoing; or under any public policy, contract or tort, or under common law; or arising under any policies,
practices or procedures of the Company; or any claim for wrongful discharge, breach of contract, infliction of emotional distress, defamation;
or any claim for costs, fees, or other expenses, including attorneys’ fees incurred in these matters) (all of the foregoing collectively referred to
herein as the “Claims”).
3.
I represent that I have made no assignment or transfer of any right, claim, demand, cause of action, or other matter covered by
paragraph 2 above.
4.
I agree that this General Release does not waive or release any rights or claims that I may have under the Age Discrimination in
Employment Act of 1967 which arise after the date I execute this General Release. I acknowledge and agree that my separation from
employment with the Company in compliance with the terms of the Agreement shall not serve as the basis for any claim or action (including,
without limitation, any claim under the Age Discrimination in Employment Act of 1967).
5.
I agree that I hereby waive all rights to sue or obtain equitable, remedial or punitive relief from any or all Released Parties of any
kind whatsoever in respect of any Claim, including, without limitation, reinstatement, back pay, front pay, and any form of injunctive relief.
Notwithstanding the above, I further acknowledge that I am not waiving and am not being required to waive any right that cannot be waived
under law, including the right to file an administrative charge or participate in an administrative investigation or proceeding; provided,
however, that I disclaim and waive any right to share or participate
2
in any monetary award resulting from the prosecution of such charge or investigation or proceeding. Additionally, I am not waiving (i) any
right to the severance benefits to which I am entitled under the Agreement, (ii) any claim relating to directors’ and officers’ liability insurance
coverage or any right of indemnification under the Company’s organizational documents or otherwise, (iii) claims under the Consolidated
Omnibus Budget Reconciliation Act of 1985, as amended, (iv) claims related to reimbursement of ordinary and reasonable business expenses
in accordance with the Company’s policies in effect from time to time, and (v) claims relating to any outstanding equity-based award on the
date of termination in accordance with the terms thereof.
6.
In signing this General Release, I acknowledge and intend that it shall be effective as a bar to each and every one of the Claims
hereinabove mentioned or implied. I expressly consent that this General Release shall be given full force and effect according to each and all
of its express terms and provisions, including those relating to unknown and unsuspected Claims (notwithstanding any state or local statute
that expressly limits the effectiveness of a general release of unknown, unsuspected and unanticipated Claims), if any, as well as those
relating to any other Claims hereinabove mentioned or implied. I acknowledge and agree that this waiver is an essential and material term of
this General Release and that without such waiver the Company would not have agreed to the terms of the Agreement. I further agree that in
the event I should bring a Claim seeking damages against the Company, or in the event I should seek to recover against the Company in any
Claim brought by a governmental agency on my behalf, this General Release shall serve as a complete defense to such Claims to the
maximum extent permitted by law. I further agree that I am not aware of any pending claim of the type described in paragraph 2 above as of
the execution of this General Release.
7.
I agree that neither this General Release, nor the furnishing of the consideration for this General Release, shall be deemed or
construed at any time to be an admission by the Company, any Released Party or myself of any improper or unlawful conduct.
8.
I agree that this General Release and the Agreement are confidential and agree not to disclose any information regarding the terms of
this General Release or the Agreement, except to my immediate family and any tax, legal or other counsel that I have consulted regarding the
meaning or effect hereof or as required by law, and I will instruct each of the foregoing not to disclose the same to anyone.
9.
Any non-disclosure provision in this General Release does not prohibit or restrict me (or my attorney) from responding to any
inquiry about this General Release or its underlying facts and
3
circumstances by the Securities and Exchange Commission (SEC), the Financial Industry Regulatory Authority (FINRA), any other self
regulatory organization or any governmental entity. In addition, nothing in this General Release prevents disclosure of information permitted
under applicable law regarding an act of sexual assault, an act of sexual harassment, an act of workplace harassment or discrimination based
on sex, or failure to prevent an act of workplace harassment or discrimination based on sex or an act of retaliation against a person for
reporting harassment or discrimination based on sex.
10.
11.
I hereby acknowledge that Sections 4 through 10 of the Agreement shall survive my execution of this General Release.
I represent that I am not aware of any claim by me other than the claims that are released by this General Release. I acknowledge that
I may hereafter discover claims or facts in addition to or different than those which I now know or believe to exist with respect to the subject
matter of the release set forth in paragraph 2 above and which, if known or suspected at the time of entering into this General Release, may
have materially affected this General Release and my decision to enter into it.
I SPECIFICALLY AND FREELY WAIVE ANY AND ALL RIGHTS I MAY HAVE UNDER CALIFORNIA CIVIL CODE SECTION
1542, WHICH STATES:
A GENERAL RELEASE DOES NOT EXTEND TO CLAIMS THAT THE CREDITOR OR RELEASING PARTY DOES NOT
KNOW OR SUSPECT TO EXIST IN HIS OR HER FAVOR AT THE TIME OF EXECUTING THE RELEASE AND THAT, IF
KNOWN BY HIM OR HER, WOULD HAVE MATERIALLY AFFECTED HIS OR HER SETTLEMENT WITH THE DEBTOR
OR RELEASED PARTY.
IN WAIVING THE PROTECTIONS OF CIVIL CODE SECTION 1542, I ACKNOWLEDGE AWARENESS OF THE ACTUAL FACTS
AND CIRCUMSTANCES SURROUNDING THE AGREEMENT UPON WHICH THIS RELEASE IS GIVEN. TO EFFECT A FULL
AND COMPLETE WAIVER AND RELEASE, I ASSUME THE RISK THAT I MAY LATER DISCOVER FACTS DIFFERENT FROM
THOSE I NOW KNOW OR BELIEVE TO BE TRUE.
12.
Notwithstanding anything in this General Release to the contrary, this General Release shall not relinquish, diminish, or in any way
affect any rights or claims arising out of any breach by the Company or by any Released Party of the Agreement after the date hereof.
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13.
Whenever possible, each provision of this General Release shall be interpreted in, such manner as to be effective and valid under
applicable law, but if any provision of this General Release is held to be invalid, illegal or unenforceable in any respect under any applicable
law or rule in any jurisdiction, such invalidity, illegality or unenforceability shall not affect any other provision or any other jurisdiction, but
this General Release shall be reformed, construed and enforced in such jurisdiction as if such invalid, illegal or unenforceable provision had
never been contained herein.
BY SIGNING THIS GENERAL RELEASE, I REPRESENT AND AGREE THAT:
1.
2.
I HAVE READ IT CAREFULLY;
I UNDERSTAND ALL OF ITS TERMS AND KNOW THAT I AM GIVING UP IMPORTANT RIGHTS, INCLUDING BUT NOT
LIMITED TO, RIGHTS UNDER THE AGE DISCRIMINATION IN EMPLOYMENT ACT OF 1967, AS AMENDED, TITLE VII OF THE
CIVIL RIGHTS ACT OF 1964, AS AMENDED; THE EQUAL PAY ACT OF 1963, THE AMERICANS WITH DISABILITIES ACT OF
1990; AND THE EMPLOYEE RETIREMENT INCOME SECURITY ACT OF 1974, AS AMENDED;
3.
4.
I VOLUNTARILY CONSENT TO EVERYTHING IN IT;
I HAVE BEEN ADVISED TO CONSULT WITH AN ATTORNEY BEFORE EXECUTING IT AND I HAVE DONE SO OR,
AFTER CAREFUL READING AND CONSIDERATION, I HAVE CHOSEN NOT TO DO SO OF MY OWN VOLITION;
5.
I HAVE HAD AT LEAST 21 DAYS FROM THE DATE OF MY RECEIPT OF THIS RELEASE TO CONSIDER IT, AND THE
CHANGES MADE SINCE MY RECEIPT OF THIS RELEASE ARE NOT MATERIAL OR WERE MADE AT MY REQUEST AND
WILL NOT RESTART THE REQUIRED 21 DAY PERIOD;
6.
I UNDERSTAND THAT I HAVE SEVEN (7) DAYS AFTER THE EXECUTION OF THIS RELEASE TO REVOKE IT AND
THAT THIS RELEASE SHALL NOT BECOME EFFECTIVE OR ENFORCEABLE UNTIL THE REVOCATION PERIOD HAS
EXPIRED;
5
7.
I HAVE SIGNED THIS GENERAL RELEASE KNOWINGLY AND VOLUNTARILY AND WITH THE ADVICE OF ANY
COUNSEL RETAINED TO ADVISE ME WITH RESPECT TO IT; AND
8.
I AGREE THAT THE PROVISIONS OF THIS GENERAL RELEASE MAY NOT BE AMENDED, WAIVED, CHANGED OR
MODIFIED EXCEPT BY AN INSTRUMENT IN WRITING SIGNED BY AN AUTHORIZED REPRESENTATIVE OF THE COMPANY
AND BY ME.
SIGNED:
NAME:
DATED:
6
AMENDED AND RESTATED EXECUTIVE EMPLOYMENT AGREEMENT
Exhibit 10.17
This Amended and Restated Executive Employment Agreement (this “Agreement”) is dated as of June 5, 2019 by and between
Axonics Modulation Technologies, Inc., a Delaware corporation (the “Company”), and Alfred Ford Jr. (“Executive”).
WHEREAS, Executive currently serves as Chief Commercial Officer of the Company pursuant to an Executive Employment
Agreement dated November 15, 2017, with a term scheduled to end on December 31, 2021 (the “Original Employment Agreement”); and
WHEREAS, the Company and Executive desire to amend and restate the Original Employment Agreement in its entirety in
accordance with the terms of this Agreement.
NOW, THEREFORE, in consideration of the premises and agreements contained herein, and for other good and valuable
consideration, the receipt and sufficiency of which are hereby acknowledged, the parties agree as follows:
1. DEFINED TERMS. Exhibit A to this Agreement sets forth defined terms for purposes of this Agreement.
2. EMPLOYMENT/TERM. The Company hereby employs Executive to perform the duties and responsibilities set forth below under
Section 3 of this Agreement, and Executive hereby accepts such employment, in each case on the terms and conditions set forth in
this Agreement. This Agreement shall commence on the Effective Date and remain in effect for five (5) years, unless earlier
terminated pursuant to Section 5 of this Agreement (the “Term”).
3. POSITION AND DUTIES.
a. Description of Executive’s Position, Duties, Authorities, and Responsibilities. Executive shall serve as the Chief Commercial
Officer of the Company. In such capacity, Executive shall (i) report to the Chief Executive Officer, (ii) devote Executive’s
full professional time and attention, best efforts, energy and skills to the services required of Executive as an employee of the
Company, except for paid time off taken in accordance with the Company’s policies and practices, and subject to the
Company’s policies pertaining to reasonable periods of absence due to sickness, personal injury or other disability; (iii) use
Executive’s best efforts to promote the interests of the Company; (iv) comply with all
1
applicable governmental laws, rules and regulations and with all of the Company’s policies, rules and regulations applicable
to employees of the Company; (v) participate in, and comply with all Company directives regarding, workplace
investigations; and (vi) discharge Executive’s responsibilities in a diligent and faithful manner, consistent with sound
business practices and in accordance with the Board’s directives.
b. Outside Boards. Executive shall obtain the written consent of the Board prior to serving on corporate, civic or charitable
boards or committees. This Section 3.b shall not be construed as preventing Executive from serving on the corporate, civic or
charitable boards or committees on which Executive serves as of the Effective Date and which have been previously
disclosed to the Board in writing; provided that in no event shall any such service or business activity require the provision
of substantial services by Executive to the operations or the affairs of such businesses or enterprises such that the provision
thereof would interfere in any respect with the performance of Executive’s duties hereunder or cause a conflict of interest to
the interests of the Company.
4. COMPENSATION AND BENEFITS.
a. Base Salary. As of the Effective Date, Executive’s Base Salary shall be three hundred fifty thousand dollars ($350,000) per
year payable in periodic installments in accordance with the Company’s regular payroll practices as in effect from time to
time. The Board or a duly authorized committee thereof will review the Base Salary on an annual basis and may increase the
Base Salary from time to time based on merit or such other considerations as the Board or a duly authorized committee
thereof may deem appropriate.
b. Commissions. Executive shall be eligible to receive commissions in accordance with a Company commission plan or
arrangement, based on performance criteria established by the Board.
c. Benefits and Vacation. Executive shall be eligible to participate in and receive the benefits under any deferred compensation
plan, health, life, accident and disability insurance plans or programs, and any other employee benefit or fringe benefit plans
or arrangements that the Company makes available generally to other senior executives of the Company, pursuant to the
provisions of such plans, programs or arrangements as in effect from time to time. Executive shall be entitled to four week’s
paid vacation and additional sick days
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in accordance with the policies of the Company for its employees generally, as in effect from time to time.
d. Equity Incentive Compensation. Executive shall be eligible to receive grants, at the discretion of the Board or a duly
authorized committee thereof, under any long-term equity- based incentive compensation plans established or maintained by
the Company for its senior executive officers, in each case subject to the terms and conditions of the applicable plans and
award documents with respect to such grants.
e. Expenses. The Company shall pay or reimburse Executive for all reasonable, ordinary and necessary business expenses
incurred or paid by Executive during the Term in the performance of Executive’s services under this Agreement in
accordance with the applicable policies and procedures of the Company as in effect from time to time, upon the presentation
of proper expense statements or such other supporting documentation as the Company may reasonably require.
5. TERMINATION OF EMPLOYMENT.
a. General. Executive’s employment may be terminated by either party at any time and for any reason; and upon termination of
Executive’s employment, the Term shall end.
b. Resignation without Good Reason. Executive may resign from employment with the Company without Good Reason by
providing the Company with at least 60 days’ advance written notice. During the Resignation Notice Period, the Company,
in its sole discretion, may elect to accelerate Executive’s date of termination of employment, it being understood that any
such termination shall still be treated as a voluntary resignation without Good Reason for purposes of this Agreement. Even
if Executive’s date of termination is accelerated, Executive shall be paid Executive’s Base Salary, and shall receive Benefits
capable of being provided to persons who are not actively employed by the Company, as if Executive had worked through
the end of the Resignation Notice Period. The Company reserves the right to require Executive not to be in the offices of the
Company or any of its affiliates and/or not to undertake all or any of Executive’s duties and/or not to contact clients,
colleagues or advisors of the Company or any of its affiliates during all or part of the Resignation Notice Period. During the
Resignation Notice Period, Executive’s terms and conditions of service and duties of loyalty and confidentiality to the
Company shall
3
remain in full force and effect and, during any such Resignation Notice Period, Executive shall continue to perform as an
employee in compliance with the terms of this Agreement and all other agreements applicable to Executive with respect to
Executive’s service with the Company or any of its affiliates.
c. Death. Executive’s employment hereunder shall terminate automatically on the date of Executive’s death.
d. Disability. At the option of the Company, Executive’s employment hereunder may be terminated immediately upon
Disability.
e. Termination for Cause. Notwithstanding any other provision of this Agreement, the Company may, at any time, immediately
terminate Executive’s employment for Cause. The Company’s lack of immediate action with respect to conduct of Executive
that would constitute Cause hereunder shall not preclude the Company from taking later action on such act or taking action
with respect to another such act committed by Executive.
f. Termination Without Cause. The Company may, at any time, immediately terminate Executive’s employment without Cause.
6. COMPENSATION UPON TERMINATION (OTHER THAN A CHANGE IN CONTROL TERMINATION). Following any
termination of Executive’s employment, the obligations of the Company to pay or provide Executive with compensation and benefits
under Section 4 shall immediately cease, and the Company shall have no further obligations to Executive under this Agreement,
except to provide (i) the Accrued Obligations, (ii) any additional amounts specifically provided by this Section 6, subject to the
applicable terms and conditions of this Section 6, and (iii) any other amounts otherwise required by law.
a. Death or Disability. If, during the Term, Executive’s employment is terminated (x) by reason of Executive’s death or (y) by
the Company for Disability, in addition to the Accrued Obligations, Executive shall receive the following compensation:
i.
The Company shall pay to Executive (or to Executive’s estate or designated beneficiary in the event of Executive’s
death) a lump sum amount equal to (A) one (1) year of Base Salary in effect as of the Termination Date, plus (B) the
annual bonus earned based on performance for the year immediately preceding the year in
4
which the Termination Date occurs, to the extent such bonus had not been paid as of the Termination Date, plus (C)
if the Termination Date occurs during the second, third or fourth quarter of a year, the Pro-Rata Bonus for that year.
Such payment shall be made in a single cash payment on the Cash Severance Commencement Date, provided that on
or before the Cash Severance Commencement Date, Executive has executed, and delivered a general waiver and
release agreement in the form of Exhibit B, attached, or in a form and with substance satisfactory to the Company,
that is no longer subject to revocation. If Executive is unable to execute and deliver such waiver and release
agreement due to death or Disability, then the waiver and release agreement shall be executed and delivered by an
authorized agent or representative of Executive and/or Executive’s estate.
ii.
As to any outstanding, unvested Equity Incentive Compensation awards on the Termination Date that are not
Performance-Based Awards, except to the extent that the applicable award agreement or equity compensation plan
provides for better treatment and notwithstanding the terms of any applicable award agreements entered into after the
Effective Date (unless such award agreements expressly reference this Agreement), Executive shall immediately vest
in such award. For any such awards that are Performance-Based Awards, vesting shall be based on the terms of the
applicable equity compensation plan and award agreement in accordance with Section 6.d. Vested stock options shall
remain exercisable during the periods provided in the applicable plan and award agreement.
b. For Cause or Without Good Reason. If, during the Term, Executive’s employment is terminated (i) by the Company for
Cause or (ii) by Executive for any reason other than for Good Reason, the Company shall pay to Executive the Accrued
Obligations.
c. Without Cause or for Good Reason (Other than a Change in Control Termination). If, during the Term, Executive’s
employment with the Company terminates by reason of a Qualifying Termination (other than a Change in Control
Termination), in addition to the Accrued Obligations, Executive shall receive the following compensation:
5
i.
Executive shall receive cash severance in an amount equal to nine (9) months of Base Salary as in effect on the
Termination Date. Such payment shall be made in a single cash payment on the Cash Severance Commencement
Date.
ii.
Executive shall be paid the annual bonus earned based on performance for the year immediately preceding the year
in which the Termination Date occurs, to the extent such bonus had not been paid as of the Termination Date. Such
bonus shall be paid at the same time bonuses are paid to other employees.
iii.
If the Termination Date occurs during the second, third or fourth quarter of a year, Executive shall be paid the Pro-
Rata Bonus for that year, made in a single cash payment on the Cash Severance Commencement Date.
iv.
Executive shall be paid an amount equal to twelve (12) months of COBRA premiums based on the terms of
Company’s group health plan and Executive’s coverage under such plan as of the Termination Date (regardless of
any COBRA election actually made by Executive or the actual COBRA coverage period under the Company’s group
health plan), payable in a single cash payment on the Cash Severance Commencement Date.
v.
As to any outstanding, unvested Equity Incentive Compensation awards on the Termination Date, for any such
awards that are Performance-Based Awards, the award shall vest at the end of the applicable performance period
based on actual performance results and prorated for the portion of the performance period worked through the
Termination Date.
All payments under clauses (i) - (v) of this Section 6.c. are conditioned on (A) Executive, on or before the Cash Severance
Commencement Date, having executed and delivered a general waiver and release agreement in the form of Exhibit B,
attached, or in a form and with substance satisfactory to the Company, that is no longer subject to revocation, and (B)
Executive’s compliance with all applicable post-employment covenants with the Company, including those set forth in
Section 8 of this Agreement.
d. Equity Incentive Compensation. Except as otherwise expressly provided herein, upon termination of Executive’s
employment during the Term, any outstanding Equity Incentive
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Compensation awards shall be forfeited or vest in accordance with the terms of the applicable plan and award agreement, and
shall be subject to such other terms and conditions of such plan and award agreement that may apply as a result of such
termination.
e. Benefits. Notwithstanding anything in this Section 6 to the contrary, the Benefits to which Executive is entitled upon or by
reason of the termination of Executive’s employment with the Company shall be subject to, and shall be governed by, the
terms and conditions of the applicable plans, programs and arrangements maintained by the Company with respect to such
Benefits. Nothing in this Agreement shall be construed to be a waiver by the Executive of any benefits accrued for or due to
the Executive under any employee benefit plan (as such term is defined in the Employee Retirement Income Security Act of
1974, as amended) maintained by the Company, if any, except that the Executive shall not be entitled to any severance
benefits pursuant to any severance plan or program of the Company other than as provided herein.
f. D&O Insurance, and Indemnification. Through at least the sixth anniversary of the Termination Date, the Company shall
maintain coverage for the Executive as a named insured on all directors’ and officers’ insurance maintained by the Company
for the benefit of its directors and officers on at least the same basis as all other covered individuals and provide the
Executive with at least the same corporate indemnification as it provides to other senior executives.
g. Expiration of Term. Notwithstanding anything in this Section 6 to the contrary, the expiration of the Term by itself shall not
entitle Executive to receipt of any payments under this Section 6.
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7. CHANGE IN CONTROL.
a. Treatment of Equity Incentive Compensation. As to any outstanding, unvested Equity Incentive Compensation awards
immediately before a Change in Control, except to the extent that the applicable award agreement or equity compensation
plan provides for better treatment and notwithstanding the terms of any applicable award agreements entered after the
Effective Date (unless such award agreements expressly reference this Agreement):
i.
For any such awards that are not Performance-Based Awards, (A) the awards shall vest in full immediately upon the
Change in Control, and (B) any vested stock options shall remain exercisable during the periods provided in the
applicable plans and award agreement.
ii.
For any such awards that are Performance-Based Awards, the award shall be fully vested based on the greater of (A)
assumed target performance or (B) performance as determined by the Board immediately before the Change in
Control.
b. Change in Control Severance. If, during the Term, Executive’s employment with the Company terminates by reason of a
Change in Control Termination, in addition to the Accrued Obligations, Executive shall receive the following compensation:
i.
Executive shall receive cash severance in an amount equal to 9 months of Base Salary as in effect on the Termination
Date. Such amount shall be payable in a single cash payment on the Cash Severance Commencement Date.
ii.
Executive shall be paid the annual bonus earned based on performance for the year immediately preceding the year
in which the Termination Date occurs, to the extent such bonus had not been paid as of the Termination Date. Such
bonus shall be paid at the same time bonuses are paid to other employees.
iii.
iv.
Executive shall be paid the Pro-Rata Bonus in a single cash payment on the Cash Severance Commencement Date.
Executive shall be paid an amount equal to 9 months of COBRA premiums based on the terms of Company’s group
health plan and Executive’s coverage under such plan as of the Termination Date (regardless of any COBRA election
actually made by Executive or the actual COBRA coverage period under the Company’s group
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health plan), payable in a single cash payment on the Cash Severance Commencement Date.
All payments under clauses (i) - (iv) of this Section 7.b. are conditioned on (A) Executive, on or before the Cash Severance
Commencement Date, having executed and delivered a general waiver and release agreement in the form of Exhibit B,
attached, or in a form and with substance satisfactory to the Company, that is no longer subject to revocation, and (B)
Executive’s compliance with all applicable post-employment covenants with the Company, including those set forth in
Section 8 of this Agreement. For avoidance of doubt, if amounts are payable to Executive under this Section 7.b, no amounts
shall be payable to Executive under Section 6.c.
8. NONSOLICITATION COVENANT. Executive agrees that Executive shall not directly or indirectly during the Term and for one
(1) year after termination of Executive’s employment, either alone or through or in conjunction with any other person or entity
employ, solicit, induce, or recruit, any person employed by any member of the Company Group at any time within the one (1) year
period immediately preceding such employment, solicitation, inducement or recruitment.
9. ADJUSTMENTS TO PAYMENTS. Anything in this Agreement to the contrary notwithstanding, in the event it shall be determined
that any payment or distribution by the Company to Executive or for Executive’s benefit (whether paid or payable or distributed or
distributable pursuant to the terms of this Agreement or otherwise) (the “Payments”) would be subject to the excise tax imposed by
Section 4999 (or any successor provisions) of the Code, or any interest or penalty is incurred by Executive with respect to such
excise tax (such excise tax, together with any such interest and penalties, is hereinafter collectively referred to as the “Excise Tax”),
then the Payments shall be reduced (but not below zero) if and to the extent that such reduction would result in Executive retaining a
larger amount, on an after-tax basis (taking into account federal, state and local income taxes and the imposition of the Excise Tax),
than if Executive received all of the Payments. The Company shall reduce or eliminate the Payments, by first reducing or eliminating
the portion of the Payments which are not payable in cash and then by reducing or eliminating cash payments, in each case in reverse
order beginning with payments or benefits which are to be paid the farthest in time from the determination. All
9
determinations required to be made under this Section, including whether and when an adjustment to any Payments is required and, if
applicable, which Payments are to be so adjusted, shall be made by an independent accounting firm selected by the Company from
among the four (4) largest accounting firms in the United States or any nationally recognized financial planning and benefits
consulting company (the “Accounting Firm”) which shall provide detailed supporting calculations both to the Company and to
Executive within fifteen (15) business days of the receipt of notice from Executive that there has been a Payment, or such earlier time
as is requested by the Company. In the event that the Accounting Firm is serving as accountant or auditor for the individual, entity or
group effecting the Change in Control, Executive shall appoint another nationally recognized accounting firm to make the
determinations required hereunder (which accounting firm shall then be referred to as the Accounting Firm hereunder). All fees and
expenses of the Accounting Firm shall be borne solely by the Company. If the Accounting Firm determines that no Excise Tax is
payable by Executive, it shall furnish Executive with a written opinion that failure to report the Excise Tax on Executive's applicable
federal income tax return would not result in the imposition of a negligence or similar penalty. Any determination by the Accounting
Firm shall be binding upon the Company and Executive.
10. COOPERATION. Upon the receipt of reasonable notice from the Company (including outside counsel), Executive agrees that while
employed by the Company and thereafter, Executive will respond and provide information with regard to matters in which Executive
has knowledge as a result of Executive’s employment with the Company, and will provide reasonable assistance to the Company, its
affiliates and their respective representatives in defense of all claims that may be made against the Company or its affiliates, and will
assist the Company and its affiliates in the prosecution of all claims that may be made by the Company or its affiliates, to the extent
that such claims may relate to the period of Executive’s employment with the Company. Executive agrees to promptly inform the
Company if Executive becomes aware of any lawsuit involving such claims that may be filed or threatened against the Company or
its affiliates. Executive also agrees to promptly inform the Company (to the extent that Executive is legally permitted to do so) if
Executive is asked to assist in any investigation of the Company or its affiliates (or their actions), regardless of whether a lawsuit or
other proceeding has then been filed against the Company or its affiliates with respect to such investigation, and shall not provide
such assistance unless legally
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required. Upon presentation of appropriate documentation, the Company shall pay or reimburse Executive for all reasonable out-of-
pocket travel, duplicating or telephonic expenses incurred by Executive in complying with this Section 10. For the first five hours of
cooperation in any calendar month during the period of cooperation, Executive shall provide the specified cooperation services
without hourly reimbursement. For each hour of cooperation or part thereof after five hours, in any calendar month, Company shall
reimburse Executive at the hourly rate determined by this fraction: (final Base Salary / 2,080 hours).
11. ARBITRATION. The parties hereby agree to submit all disputes, claims and controversies (“Claims”) between the parties or related
to or arising out of their employment relationship by and between the Company and Executive to final, binding arbitration to the
fullest extent permitted by law. The Federal Arbitration Act., 9 U.S.C. § 1 et seq., shall govern the interpretation and enforcement of
this Section 11. The court and not the arbitrator will determine matters of enforceability of this Section 11.
a. Statute of Limitations. The statutory limitations period applicable to a Claim asserted in a civil action shall apply to any such
Claim asserted in any arbitration proceeding under this Section 11. Arbitration is commenced for limitations purposes by
submitting the matter to the arbitral forum.
b.
Individual Basis. All Claims that are subject to arbitration under this Section 11 must and will take place on an individual
basis only.
c. Venue. Binding arbitration under this Section 11 shall be conducted in California unless required by law to be conducted
elsewhere, in which case it shall be conducted where required by law.
d. Applicable Rules. The arbitration proceeding, including discovery, shall be conducted in accordance with the Federal
Arbitration Act, the JAMS Policy on Employment Arbitration Minimum Standards and the JAMS Employment Arbitration
Rules and Procedures then in effect (the “JAMS Rules”). Executive understands that if Executive wishes to receive a copy of
the JAMS Rules currently in effect, Executive may inform the Company in writing, and the Company will provide them to
Executive before Executive executes this Agreement. Executive also understand that JAMS Rules are available online at
http://www.jamsadr.com/rules-employment-arbitration/.
11
e. Arbitrator Selection. The arbitration shall be conducted before a neutral arbitrator selected by all parties in accordance with
JAMS Rules.
f. Cost Allocation. If required by applicable law, the Company shall pay all additional costs peculiar to the arbitration to the
extent such costs would not otherwise be incurred in a court proceeding (for instance, the Company shall pay the arbitrator’s
fees, and the JAMS administration and filing fees, to the extent such fees exceed court filing fees).
g. Attorneys’ Fees and Costs. Each party shall pay such party’s own costs and attorneys’ fees except that the arbitrator shall
award costs and attorneys’ fees to the prevailing party.
h. Written Decision. The arbitrator shall follow applicable substantive law and, within 30 days after the conclusion of the
arbitration, issue a written opinion setting forth the factual and legal bases for his or her decision.
i. Acknowledgement. EXECUTIVE UNDERSTANDS THAT EXECUTIVE IS GIVING UP EXECUTIVE’S RIGHT TO A
JURY TRIAL BY ENTERING INTO THIS AGREEMENT. EXECUTIVE UNDERSTANDS THAT EXECUTIVE IS
GIVING UP EXECUTIVE’S RIGHT TO COMMENCE OR PARTICIPATE IN A CLASS OR COLLECTIVE ACTION
AND INSTEAD AGREES TO ARBITRATE ANY EMPLOYMENT-RELATED DISPUTE ON AN INDIVIDUAL BASIS
ONLY TO THE MAXIMUM EXTENT PERMITTED BY LAW.
12. CODE SECTION 409A.
a. This Agreement is intended to comply with the requirements of Section 409A of the Internal Revenue Code of 1986, as
amended (“Section 409A”), including the exceptions thereto, and shall be construed and administered in accordance with
such intent. Notwithstanding any other provision of this Agreement, payments provided under this Agreement may only be
made upon an event and in a manner that complies with Section 409A or an applicable exemption. Any payments under this
Agreement that may be excluded from Section 409A either as separation pay due to an involuntary separation from service
or as a short-term deferral shall be excluded from Section 409A to the maximum extent possible. For purposes of Section
409A, each separate payment or installment payment provided under this Agreement shall be treated as a separate payment.
Any
12
payments to be made under this Agreement in connection with a termination of employment shall only be made if such
termination of employment constitutes a “separation from service” under Section 409A. Notwithstanding the foregoing, the
Company makes no representations that the payments and benefits provided under this Agreement comply with Section
409A and in no event shall the Company be liable for all or any portion of any taxes, penalties, interest or other expenses that
may be incurred by Executive on account of non-compliance with Section 409A.
b. Notwithstanding any other provision of this Agreement, if at the time of Executive’s termination of employment, Executive
is a “specified employee,” determined in accordance with Section 409A, any payments and benefits provided under this
Agreement that constitute “nonqualified deferred compensation” subject to Section 409A that are provided to Executive on
account of Executive’s separation from service shall not be paid until the first payroll date to occur following the six-month
anniversary of Executive’s termination date (“Specified Employee Payment Date”). The aggregate amount of any payments
that would otherwise have been made during such six-month period shall be paid in a lump sum on the Specified Employee
Payment Date and thereafter, any remaining payments shall be paid without delay in accordance with their original schedule.
If Executive dies before the Specified Employee Payment Date, any delayed payments shall be paid to Executive’s estate in a
lump sum within one week of Executive’s death.
c. To the extent required by Section 409A, each reimbursement or in-kind benefit provided under this Agreement shall be
provided in accordance with the following: (i) the amount of expenses eligible for reimbursement, or in-kind benefits
provided, during each calendar year cannot affect the expenses eligible for reimbursement, or in-kind benefits to be provided,
in any other calendar year; (ii) any reimbursement of an eligible expense shall be paid to Executive on or before the last day
of the calendar year following the calendar year in which the expense was incurred; and (iii) any right to reimbursements or
in-kind benefits under this Agreement shall not be subject to liquidation or exchange for another benefit. Any tax gross-up
payments provided under this Agreement shall be paid to Executive on or before December 31 of the calendar year
immediately following the calendar year in which Executive remits the related taxes.
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d. Whenever in this Agreement a payment or benefit is conditioned on Executive’s execution of a release of claims, such
release must be executed, and all revocation periods shall have expired within 60 days after the Termination Date; failing
which such payment or benefit shall be forfeited. If such payment or benefit constitutes “nonqualified deferred
compensation” subject to Section 409A, and if such 60-day period begins in one calendar year and ends in the next calendar
year, the payment or benefit shall not be made or commence before the second such calendar year, even if the release
becomes irrevocable in the first such calendar year.
13. GENERAL PROVISIONS.
a. Notices. All notices, requests, demands, statements, reports and other communications provided for by this Agreement shall
be in writing (email being sufficient) and shall be sent by (i) certified mail, return receipt requested, postage prepaid, (ii)
nationally recognized overnight delivery service, (iii) personal delivery or (iv) email. A notice shall be deemed to be given
(x) if notice is delivered by certified mail or nationally recognized overnight delivery service, on the business day following
the date of its mailing, (y) if such notice is delivered personally, upon delivery, or (z) if such notice is sent by email, upon
sending. Each party may change such party’s address for notices by giving notice in accordance herewith. All notices shall
be addressed and mailed or delivered to the following addresses:
If to the COMPANY:
Attn: Chief Executive Officer
Axonics Modulation Technologies, Inc. 26 Technology Drive
Irvine, CA 92618
If to EXECUTIVE:
Alfred Ford Jr.
46 Broadway
Rockville Center, NY 11570
b. Entire Agreement. This Agreement constitutes the entire agreement between the parties with respect to the subject matter
hereof and supersedes all prior agreements,
14
representations and understandings (whether written or oral) of the parties with respect to the subject matter hereof, including
the Original Employment Agreement, and any other agreement between Executive and the Company or any of its affiliates
and subsidiaries.
c. Modification and Waiver. No amendment or variation of the terms of this Agreement shall be valid unless made in writing
and signed by Executive and a duly authorized representative of the Company (other than Executive). A waiver of any term
or condition of this Agreement shall not be construed as a general waiver by the Company. If one or more provisions of this
Agreement are held to be illegal or unenforceable under applicable law, such illegal or unenforceable provision(s) shall be
limited or excluded from this Agreement to the minimum extent required so that this Agreement shall otherwise remain in
full force and effect and enforceable in accordance with its terms.
d. Governing Law. This Agreement shall be governed by and construed in accordance with the laws of the State of California,
without giving effect to its conflict of law principles, and any dispute in the meaning, effect or validity of this Agreement
shall be resolved in accordance with the laws of the State of California.
e. Assignment; Binding Effect. This Agreement is fully assignable and transferable by the Company, but any purported
assignment or transfer by Executive is void. It is hereby agreed that Executive’s rights and obligations under this Agreement
are personal and not assignable by Executive. This Agreement shall be binding upon and inure to the benefit of the heirs,
legal representatives, successors and permitted assigns of the parties. EXECUTIVE HAS READ THIS AGREEMENT
CAREFULLY AND UNDERSTANDS AND ACCEPTS THE OBLIGATIONS WHICH IT IMPOSES UPON
EXECUTIVE WITHOUT RESERVATION. NO PROMISES OR REPRESENTATIONS HAVE BEEN MADE TO
EXECUTIVE TO INDUCE EXECUTIVE TO SIGN THIS AGREEMENT. EXECUTIVE SIGNS THIS
AGREEMENT VOLUNTARILY AND FREELY, IN DUPLICATE, WITH THE UNDERSTANDING THAT THE
COMPANY WILL RETAIN ONE COUNTERPART AND THE OTHER COUNTERPART WILL BE RETAINED
BY EXECUTIVE.
15
f.
Injunctive Relief. Executive agrees that any breach of this Agreement will cause irreparable harm to the Company for which
damages would not be an adequate remedy, and, therefore, to the fullest extent permitted by applicable law, the Company
will be entitled to injunctive relief with respect thereto in addition to any other remedies and without any requirement to post
bond.
g. Survival. This Agreement shall terminate upon the expiration of the Term; provided that the provisions of Section 1 and
Sections 6 through 13 shall survive termination of this Agreement and termination of Executive’s employment regardless of
the reason for such termination.
h. Withholding. The Company may withhold from any and all amounts payable under this Agreement or otherwise such
federal, state and local taxes as may be required to be withheld pursuant to applicable law.
[Signature page follows]
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In witness whereof, the parties have executed this Agreement as of the date first above written.
COMPANY:
Axonics Modulation Technologies, Inc.
By: /s/ Raymond W. Cohen
Raymond W. Cohen
Chief Executive Officer
EXECUTIVE:
/s/ Alfred Ford Jr.
Alfred Ford Jr.
Signature Page to Amended and Restated Executive Employment Agreement
EXHIBIT A
For purposes of interpreting the Agreement, the following definitions shall apply:
“Accrued Obligations” means, in connection with Executive’s termination of employment with the Company for any reason, (i) any
unpaid Base Salary accrued through the Termination Date, payable as soon as practicable (not more than 30 days) after the Termination Date,
and (ii) any unpaid Benefits accrued through the Termination Date to which Executive is entitled under any plans, programs or arrangements
applicable to terminated employees in which Executive participates, payable in accordance with the terms of such plans, programs or
arrangements.
“Base Salary” means Executive’s annual rate of base salary from the Company as provided in Section 4.a (including any permitted
adjustments to the annual rate of base salary during the Term as provided by Section 4.a).
“Benefits” means the employee benefits provided to Executive by the Company under the provisions of Section 4.c.
“Board” means the Board of Directors of the Company.
“Cash Severance Commencement Date” means the 60th day after the Termination Date.
“Cause” means the occurrence of any of the following by Executive: (i) fraud, misappropriation, embezzlement or acts of similar
dishonesty; (ii) conviction of, or plea of nolo contendere to, a felony; (iii) excessive use of alcohol or illegal use of drugs in the workplace;
(iv) gross negligence or intentional or willful misconduct by Executive in the performance of Executive’s duties; (v) breach of Executive’s
duty of loyalty to the Company or diversion or usurpation of corporate opportunities properly belonging to the Company; (vi) the knowing
breach of the Company’s confidentiality agreement to which the Executive is a party to; or (vii) violation of any material provision of this
Agreement or any other material provision of any other agreement between Executive and the Company.
“Change in Control” means a “Change in Control” as defined under the Axonics Modulation Technologies, Inc. 2018 Omnibus
Incentive Plan.
“Change in Control Protected Period” means the period commencing on the date of a Change in Control and ending on first
anniversary of the date of the Change in Control.
“Change in Control Termination” means a Qualifying Termination that occurs during the Change in Control Protected Period.
“Disability” means any physical or mental illness, impairment or incapacity which, in the good faith determination of the Board, has
prevented Executive from performing the essential functions of Executive’s position hereunder for a period of 90 or more consecutive days
(or for shorter periods totaling 120 days) during any period of 12 consecutive months, consistent with applicable law.
“Effective Date” means July 1, 2019, the effective date of this Agreement and the first day of the Term.
“Equity Incentive Compensation” means the equity compensation awards provided to Executive by the Company under Section 4.d.
“Good Reason” means the occurrence of any of the following events, without the express consent of Executive, (i) a material
diminution in Executive’s Base Salary, or (ii) a material diminution in Executive’s position, duties, authorities or responsibilities (other than
temporarily while physically or mentally incapacitated or as required by applicable law). In order for Executive to terminate Executive’s
employment for Good Reason, (x) Executive must furnish written notice to the Company setting forth the facts and circumstances claimed to
provide a basis for such resignation within 30 days following the occurrence of such facts and circumstances, (y) the Company shall have 30
days after its receipt of such written notice to cure such facts and circumstances in all material respects (and if so cured, then Executive shall
not be permitted to resign for Good Reason in respect thereof), and (z) Executive must actually terminate Executive’s employment within 30
days following the expiration of the Company’s cure period set forth above.
“Performance-Based Award” means an option, restricted stock or other Equity Incentive Compensation award that vests based on
performance-based criteria.
“Pro-Rata Bonus” means an amount determined as of Executive’s Termination Date as follows: (i) if Executive’s termination of
employment is due to Executive’s death or Disability or by reason of a Qualifying Termination that is not a Change in Control Termination,
the Pro-Rata Bonus shall equal the actual annual cash bonus earned based on performance through the Termination Date as determined by the
Board, multiplied by the Pro-Rata Fraction, payable in a lump sum at the time specified in Section 6.a or Section 6.c (as applicable); and (ii)
if Executive’s termination of employment is due to a Change in
Control Termination, the Pro-Rata Bonus shall equal the target annual cash bonus for the year in which the Termination Date occurs,
multiplied by the Pro-Rata Fraction, and payable in a lump sum at the time specified in Section 7.b.
“Pro-Rata Fraction” means a fraction, the numerator of which is the number of days in the calendar year through Executive’s
Termination Date and the denominator of which is 365.
“Qualifying Termination” means a termination of Executive’s employment with the Company during the Term either (i) by the
Company other than for Cause, or (ii) by Executive with Good Reason.
“Resignation Notice Period” means the period, not less than 60 days, between the date Executive provides the Company with
written notice of his intent to resign from employment with the Company and the intended effective date of such resignation.
“Termination Date” means the date of Executive’s termination of employment with the Company as determined under this
Agreement.
EXHIBIT B
GENERAL RELEASE
I, ___________ in consideration of and subject to the performance by Axonics Modulation Technologies, Inc. (together with its
subsidiaries and successors, the “Company”), of its obligations under the Amended and Restated Executive Employment Agreement dated as
of ___________, 2019 (the “Agreement”), do hereby release and forever discharge as of the date hereof the Company and its respective
affiliates, subsidiaries and direct or indirect parent entities and all present, former and future directors, officers, agents, representatives,
employees, successors and assigns of the Company and/or its respective affiliates, subsidiaries and direct or indirect parent entities
(collectively, the “Released Parties”) to the extent provided below (this “General Release”). The Released Parties are intended to be third-
party beneficiaries of this General Release, and this General Release may be enforced by each of them in accordance with the terms hereof in
respect of the rights granted to such Released Parties hereunder. Terms used herein but not otherwise defined shall have the meanings given
to them in the Agreement.
1.
I understand that any payments or benefits paid or granted to me under the Agreement represent, in part, consideration for signing
this General Release and are not salary, wages or benefits to which I was already entitled. I understand and agree that I will not receive
certain of the payments and benefits specified in the Agreement unless I execute this General Release and do not revoke this General Release
within the time period permitted hereafter. Such payments and benefits will not be considered compensation for purposes of any employee
benefit plan, program, policy or arrangement maintained or hereafter established by the Company or its affiliates.
2.
Except as provided in paragraphs 4 and 5 below and except for the provisions of the Agreement which expressly survive the
termination of my employment with the Company, I knowingly and voluntarily (for myself, my heirs, executors, administrators and assigns)
release and forever discharge the Company and the other Released Parties from any and all claims, suits, controversies, actions, causes of
action, cross-claims, counter claims, demands, debts, compensatory damages, liquidated damages, punitive or exemplary damages, other
damages, claims for costs and attorneys’ fees, or liabilities of any nature whatsoever in law and in equity, both past and present (through the
date that this General Release becomes effective and enforceable) and whether known or unknown, suspected, or claimed against the
Company or any of the Released Parties which I, my spouse, or any of my heirs, executors, administrators or assigns, may have, which arise
out of or are connected with my employment with, or my separation or
1
termination from, the Company (including, but not limited to, any allegation, claim or violation, arising under: Title VII of the Civil Rights
Act of 1964, as amended; the Civil Rights Act of 1991; the Age Discrimination in Employment Act of 1967, as amended (including the
Older Workers Benefit Protection Act); the Equal Pay Act of 1963, as amended; the Americans with Disabilities Act of 1990; the Americans
with Disabilities Act Amendments Act of 2008; the Family and Medical Leave Act of 1993; the Labor Management Relations Act; the
Worker Adjustment Retraining and Notification Act; the Employee Retirement Income Security Act of 1974; the Sarbanes-Oxley Act of
2002; the California Worker Adjustment Retraining and Notification Act; the California Fair Employment and Housing Act; the California
Labor Code; the California Family Rights Act; the California Industrial Welfare Commission Wage Orders; the California Constitution; the
California Government Code; any applicable Executive Order Programs; the Fair Labor Standards Act; or their state or local counterparts; or
under any other federal, state or local civil or human rights law, or under any other local, state, or federal law, regulation or ordinance, as well
as any amendments to any of the foregoing; or under any public policy, contract or tort, or under common law; or arising under any policies,
practices or procedures of the Company; or any claim for wrongful discharge, breach of contract, infliction of emotional distress, defamation;
or any claim for costs, fees, or other expenses, including attorneys’ fees incurred in these matters) (all of the foregoing collectively referred to
herein as the “Claims”).
3.
I represent that I have made no assignment or transfer of any right, claim, demand, cause of action, or other matter covered by
paragraph 2 above.
4.
I agree that this General Release does not waive or release any rights or claims that I may have under the Age Discrimination in
Employment Act of 1967 which arise after the date I execute this General Release. I acknowledge and agree that my separation from
employment with the Company in compliance with the terms of the Agreement shall not serve as the basis for any claim or action (including,
without limitation, any claim under the Age Discrimination in Employment Act of 1967).
5.
I agree that I hereby waive all rights to sue or obtain equitable, remedial or punitive relief from any or all Released Parties of any
kind whatsoever in respect of any Claim, including, without limitation, reinstatement, back pay, front pay, and any form of injunctive relief.
Notwithstanding the above, I further acknowledge that I am not waiving and am not being required to waive any right that cannot be waived
under law, including the right to file an administrative charge or participate in an administrative investigation or proceeding; provided,
however, that I disclaim and waive any right to share or participate
2
in any monetary award resulting from the prosecution of such charge or investigation or proceeding. Additionally, I am not waiving (i) any
right to the severance benefits to which I am entitled under the Agreement, (ii) any claim relating to directors’ and officers’ liability insurance
coverage or any right of indemnification under the Company’s organizational documents or otherwise, (iii) claims under the Consolidated
Omnibus Budget Reconciliation Act of 1985, as amended, (iv) claims related to reimbursement of ordinary and reasonable business expenses
in accordance with the Company’s policies in effect from time to time, and (v) claims relating to any outstanding equity-based award on the
date of termination in accordance with the terms thereof.
6.
In signing this General Release, I acknowledge and intend that it shall be effective as a bar to each and every one of the Claims
hereinabove mentioned or implied. I expressly consent that this General Release shall be given full force and effect according to each and all
of its express terms and provisions, including those relating to unknown and unsuspected Claims (notwithstanding any state or local statute
that expressly limits the effectiveness of a general release of unknown, unsuspected and unanticipated Claims), if any, as well as those
relating to any other Claims hereinabove mentioned or implied. I acknowledge and agree that this waiver is an essential and material term of
this General Release and that without such waiver the Company would not have agreed to the terms of the Agreement. I further agree that in
the event I should bring a Claim seeking damages against the Company, or in the event I should seek to recover against the Company in any
Claim brought by a governmental agency on my behalf, this General Release shall serve as a complete defense to such Claims to the
maximum extent permitted by law. I further agree that I am not aware of any pending claim of the type described in paragraph 2 above as of
the execution of this General Release.
7.
I agree that neither this General Release, nor the furnishing of the consideration for this General Release, shall be deemed or
construed at any time to be an admission by the Company, any Released Party or myself of any improper or unlawful conduct.
8.
I agree that this General Release and the Agreement are confidential and agree not to disclose any information regarding the terms of
this General Release or the Agreement, except to my immediate family and any tax, legal or other counsel that I have consulted regarding the
meaning or effect hereof or as required by law, and I will instruct each of the foregoing not to disclose the same to anyone.
9.
Any non-disclosure provision in this General Release does not prohibit or restrict me (or my attorney) from responding to any
inquiry about this General Release or its underlying facts and
3
circumstances by the Securities and Exchange Commission (SEC), the Financial Industry Regulatory Authority (FINRA), any other self
regulatory organization or any governmental entity. In addition, nothing in this General Release prevents disclosure of information permitted
under applicable law regarding an act of sexual assault, an act of sexual harassment, an act of workplace harassment or discrimination based
on sex, or failure to prevent an act of workplace harassment or discrimination based on sex or an act of retaliation against a person for
reporting harassment or discrimination based on sex.
10.
11.
I hereby acknowledge that Sections 4 through 10 of the Agreement shall survive my execution of this General Release.
I represent that I am not aware of any claim by me other than the claims that are released by this General Release. I acknowledge that
I may hereafter discover claims or facts in addition to or different than those which I now know or believe to exist with respect to the subject
matter of the release set forth in paragraph 2 above and which, if known or suspected at the time of entering into this General Release, may
have materially affected this General Release and my decision to enter into it.
I SPECIFICALLY AND FREELY WAIVE ANY AND ALL RIGHTS I MAY HAVE UNDER CALIFORNIA CIVIL CODE SECTION
1542, WHICH STATES:
A GENERAL RELEASE DOES NOT EXTEND TO CLAIMS THAT THE CREDITOR OR RELEASING PARTY DOES NOT
KNOW OR SUSPECT TO EXIST IN HIS OR HER FAVOR AT THE TIME OF EXECUTING THE RELEASE AND THAT, IF
KNOWN BY HIM OR HER, WOULD HAVE MATERIALLY AFFECTED HIS OR HER SETTLEMENT WITH THE DEBTOR
OR RELEASED PARTY.
IN WAIVING THE PROTECTIONS OF CIVIL CODE SECTION 1542, I ACKNOWLEDGE AWARENESS OF THE ACTUAL FACTS
AND CIRCUMSTANCES SURROUNDING THE AGREEMENT UPON WHICH THIS RELEASE IS GIVEN. TO EFFECT A FULL
AND COMPLETE WAIVER AND RELEASE, I ASSUME THE RISK THAT I MAY LATER DISCOVER FACTS DIFFERENT FROM
THOSE I NOW KNOW OR BELIEVE TO BE TRUE.
12.
Notwithstanding anything in this General Release to the contrary, this General Release shall not relinquish, diminish, or in any way
affect any rights or claims arising out of any breach by the Company or by any Released Party of the Agreement after the date hereof.
4
13.
Whenever possible, each provision of this General Release shall be interpreted in, such manner as to be effective and valid under
applicable law, but if any provision of this General Release is held to be invalid, illegal or unenforceable in any respect under any applicable
law or rule in any jurisdiction, such invalidity, illegality or unenforceability shall not affect any other provision or any other jurisdiction, but
this General Release shall be reformed, construed and enforced in such jurisdiction as if such invalid, illegal or unenforceable provision had
never been contained herein.
BY SIGNING THIS GENERAL RELEASE, I REPRESENT AND AGREE THAT:
1.
2.
I HAVE READ IT CAREFULLY;
I UNDERSTAND ALL OF ITS TERMS AND KNOW THAT I AM GIVING UP IMPORTANT RIGHTS, INCLUDING BUT NOT
LIMITED TO, RIGHTS UNDER THE AGE DISCRIMINATION IN EMPLOYMENT ACT OF 1967, AS AMENDED, TITLE VII OF THE
CIVIL RIGHTS ACT OF 1964, AS AMENDED; THE EQUAL PAY ACT OF 1963, THE AMERICANS WITH DISABILITIES ACT OF
1990; AND THE EMPLOYEE RETIREMENT INCOME SECURITY ACT OF 1974, AS AMENDED;
3.
4.
I VOLUNTARILY CONSENT TO EVERYTHING IN IT;
I HAVE BEEN ADVISED TO CONSULT WITH AN ATTORNEY BEFORE EXECUTING IT AND I HAVE DONE SO OR,
AFTER CAREFUL READING AND CONSIDERATION, I HAVE CHOSEN NOT TO DO SO OF MY OWN VOLITION;
5.
I HAVE HAD AT LEAST 21 DAYS FROM THE DATE OF MY RECEIPT OF THIS RELEASE TO CONSIDER IT, AND THE
CHANGES MADE SINCE MY RECEIPT OF THIS RELEASE ARE NOT MATERIAL OR WERE MADE AT MY REQUEST AND
WILL NOT RESTART THE REQUIRED 21 DAY PERIOD;
6.
I UNDERSTAND THAT I HAVE SEVEN (7) DAYS AFTER THE EXECUTION OF THIS RELEASE TO REVOKE IT AND
THAT THIS RELEASE SHALL NOT BECOME EFFECTIVE OR ENFORCEABLE UNTIL THE REVOCATION PERIOD HAS
EXPIRED;
5
7.
I HAVE SIGNED THIS GENERAL RELEASE KNOWINGLY AND VOLUNTARILY AND WITH THE ADVICE OF ANY
COUNSEL RETAINED TO ADVISE ME WITH RESPECT TO IT; AND
8.
I AGREE THAT THE PROVISIONS OF THIS GENERAL RELEASE MAY NOT BE AMENDED, WAIVED, CHANGED OR
MODIFIED EXCEPT BY AN INSTRUMENT IN WRITING SIGNED BY AN AUTHORIZED REPRESENTATIVE OF THE COMPANY
AND BY ME.
SIGNED:
NAME:
DATED:
6
List of Subsidiaries of
Axonics, Inc.
Exhibit 21.1
Name of Subsidiary
Axonics Europe, S.A.S.
Axonics Modulation Technologies, U.K. Limited
Axonics Modulation Technologies Australia Pty Ltd
Axonics Women’s Health Limited
Bulkamid SARL
Axonics GmbH
Contura, Inc.
Jurisdiction of Incorporation or Organization
France
England and Wales
Australia
England and Wales
France
Germany
United States
Consent of Independent Registered Public Accounting Firm
Exhibit 23.1
Axonics, Inc.
Irvine, California
We hereby consent to the incorporation by reference in the Registration Statements on Form S-3 (No. 333-234546) and Form S-8 (No.333-228170) of
Axonics, Inc. (“Company”) of our reports dated March 1, 2023, relating to the consolidated financial statements and the effectiveness of the Company’s
internal control over financial reporting, which appear in this Form 10-K. Our report on the effectiveness of the internal control over financial reporting
expresses an adverse opinion on the effectiveness of the Company’s internal control over financial reporting as of December 31, 2022.
/s/ BDO USA, LLP
Costa Mesa, California
March 1, 2023
CERTIFICATION OF PRINCIPAL EXECUTIVE OFFICER PURSUANT TO RULE 13a-14(a) OR RULE 15d-14(a) OF THE SECURITIES
EXCHANGE ACT OF 1934, AS AMENDED
Exhibit 31.1
I, Raymond W. Cohen, certify that:
1. I have reviewed this Annual Report on Form 10-K of Axonics, Inc.;
2. Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the
statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this
report;
3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the
financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;
4. The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in
Exchange Act Rules 13a-15(e) and 15d-15(e)) for the registrant and have:
(a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision,
to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within
those entities, particularly during the period in which this report is being prepared;
b) Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our
supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for
external purposes in accordance with generally accepted accounting principles;
c) Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the
effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and
d) Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent
fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to
materially affect, the registrant’s internal control over financial reporting; and
5. The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the
registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions):
a) All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are
reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
b) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal
control over financial reporting.
Date: March 1, 2023
By:
/s/ Raymond W. Cohen
Raymond W. Cohen
Chief Executive Officer and Director
(Principal Executive Officer)
CERTIFICATION OF PRINCIPAL FINANCIAL OFFICER PURSUANT TO RULE 13a-14(a) OR RULE 15d-14(a) OF THE SECURITIES
EXCHANGE ACT OF 1934, AS AMENDED
Exhibit 31.2
I, Dan L. Dearen, certify that:
1. I have reviewed this Annual Report on Form 10-K of Axonics, Inc.;
2. Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to make the
statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this
report;
3. Based on my knowledge, the financial statements, and other financial information included in this report, fairly present in all material respects the
financial condition, results of operations and cash flows of the registrant as of, and for, the periods presented in this report;
4. The registrant’s other certifying officer and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in
Exchange Act Rules 13a-15(e) and 15d-15(e)) for the registrant and have:
(a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision,
to ensure that material information relating to the registrant, including its consolidated subsidiaries, is made known to us by others within
those entities, particularly during the period in which this report is being prepared;
b) Designed such internal control over financial reporting, or caused such internal control over financial reporting to be designed under our
supervision, to provide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for
external purposes in accordance with generally accepted accounting principles;
c) Evaluated the effectiveness of the registrant’s disclosure controls and procedures and presented in this report our conclusions about the
effectiveness of the disclosure controls and procedures, as of the end of the period covered by this report based on such evaluation; and
d) Disclosed in this report any change in the registrant’s internal control over financial reporting that occurred during the registrant’s most recent
fiscal quarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to
materially affect, the registrant’s internal control over financial reporting; and
5. The registrant’s other certifying officer and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to the
registrant’s auditors and the audit committee of the registrant’s board of directors (or persons performing the equivalent functions):
a) All significant deficiencies and material weaknesses in the design or operation of internal control over financial reporting which are
reasonably likely to adversely affect the registrant’s ability to record, process, summarize and report financial information; and
b) Any fraud, whether or not material, that involves management or other employees who have a significant role in the registrant’s internal
control over financial reporting.
Date: March 1, 2023
By:
/s/ Dan L. Dearen
Dan L. Dearen
President and Chief Financial Officer
(Principal Financial Officer)
CERTIFICATION PURSUANT TO
18 U.S.C. SECTION 1350, AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
Exhibit 32.1
In connection with the Annual Report of Axonics, Inc. (the “Company”) on Form 10-K for the fiscal year ended December 31, 2022 as filed with the
Securities and Exchange Commission on the date hereof (the “Report”), I certify, pursuant to 18 U.S.C. § 1350, as adopted pursuant to § 906 of the
Sarbanes-Oxley Act of 2002, that:
(1) The Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended; and
(2) The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.
Date: March 1, 2023
By:
/s/ Raymond W. Cohen
Raymond W. Cohen
Chief Executive Officer and Director
(Principal Executive Officer)
A signed original of this written statement required by Section 906 has been provided to Axonics, Inc. and will be retained by Axonics, Inc. and furnished
to the Securities and Exchange Commission or its staff upon request.
CERTIFICATION PURSUANT TO
18 U.S.C. SECTION 1350, AS ADOPTED PURSUANT TO
SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002
Exhibit 32.2
In connection with the Annual Report of Axonics, Inc. (the “Company”) on Form 10-K for the fiscal year ended December 31, 2022 as filed with the
Securities and Exchange Commission on the date hereof (the “Report”), I certify, pursuant to 18 U.S.C. § 1350, as adopted pursuant to § 906 of the
Sarbanes-Oxley Act of 2002, that:
(1) The Report fully complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934, as amended; and
(2) The information contained in the Report fairly presents, in all material respects, the financial condition and results of operations of the Company.
Date: March 1, 2023
By:
/s/ Dan L. Dearen
Dan L. Dearen
President and Chief Financial Officer
(Principal Financial Officer)
A signed original of this written statement required by Section 906 has been provided to Axonics, Inc. and will be retained by Axonics, Inc. and furnished
to the Securities and Exchange Commission or its staff upon request.