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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: September 24, 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: 1-36214
__________________________________________________________
HOLOGIC, INC.
(Exact name of registrant as specified in its charter)
Delaware
(State or Other Jurisdiction of
Incorporation or Organization)
04-2902449
(I.R.S. Employer Identification No.)
250 Campus Drive, Marlborough, Massachusetts 01752
(Address of Principal Executive Offices) (Zip Code)
Registrant’s Telephone Number, Including Area Code (508) 263-2900
Securities registered pursuant to Section 12(b) of the Act:
Title of Each Class
Common Stock, $0.01 par value
Trading Symbol(s)
HOLX
Name of Each Exchange on which Registered
The NASDAQ Global Select Market
Securities registered pursuant to Section 12(g) of the Act: None
__________________________________________________________
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,
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 (Check one).
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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. ☒
Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Act.) Yes ☐ No ☒
The aggregate market value of the registrant's Common Stock held by non-affiliates of the registrant as of March 26,
2022 was $18,757,846,271 based on the price of the last reported sale on NASDAQ Global Select Market on that date.
As of November 10, 2022, 245,833,759 shares of the registrant’s Common Stock, $0.01 par value, were outstanding.
__________________________________________________________
DOCUMENTS INCORPORATED BY REFERENCE
Portions of the registrant’s Proxy Statement for the registrant’s annual meeting of stockholders to be filed within 120 days
of the end of its fiscal year ended September 24, 2022 are incorporated into Part III (Items 10, 11, 12, 13 and 14) of this Annual
Report on Form 10-K where indicated.
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HOLOGIC, INC.
ANNUAL REPORT ON FORM 10-K
For the Fiscal Year Ended September 24, 2022
TABLE OF CONTENTS
PART I
Page
Item 1.
Business
Item 1A. Risk Factors
Item 1B. Unresolved Staff Comments
Item 2.
Properties
Item 3.
Legal Proceedings
Item 4. Mine Safety Disclosures
PART II
Item 5. Market for Registrant's Common Equity, Related Stockholder Matters and Issuer Purchases of
Equity Securities
Item 6.
Reserved
Item 7. Management's Discussion and Analysis of Financial Condition and Results of Operations
Item 7A. Quantitative and Qualitative Disclosures About Market Risk
Item 8.
Financial Statements and Supplementary Data
Item 9.
Changes in and Disagreements with Accountants on Accounting and Financial Disclosure
Item 9A. Controls and Procedures
Item 9B. Other Information
Item 10. Directors, Executive Officers and Corporate Governance
Item 11.
Executive Compensation
PART III
Item 12.
Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters
Item 13. Certain Relationships and Related Transactions, and Director Independence
Item 14.
Principal Accounting Fees and Services
Item 15.
Exhibits and Financial Statement Schedules
Item 16.
Form 10-K Summary
PART IV
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SPECIAL NOTE REGARDING FORWARD-LOOKING STATEMENTS
Some of the statements contained in this report and documents incorporated by reference herein are 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"). These statements involve known and unknown
risks, uncertainties and other factors which may cause our or our industry’s actual results, performance or achievements to be
materially different from any future results, performance or achievements expressed or implied by the forward-looking
statements. Forward-looking statements may include, but are not limited to, statements regarding:
•
the ongoing and possible future effects of global challenges, including macroeconomic uncertainties, the war in Ukraine,
other economic disruptions and U.S. and global recession concerns, on our customers and suppliers and on our business,
financial condition, results of operations and cash flows and our ability to draw down our revolver;
•
• the effect of the worldwide political and social uncertainty and divisions, including the impact on trade regulation and
tariffs, that may adversely impact the cost and sale of our products in certain countries, or increase the costs we may incur
to purchase materials, parts and equipment from our suppliers;
the ongoing and possible future effects of supply chain constraints, including the availability of critical raw materials and
components, including semiconductor chips, as well as cost inflation in materials, packaging and transportation;
the possibility of interruptions or delays at our manufacturing facilities, or the failure to secure alternative suppliers if any
of our sole source third-party manufacturers fail to supply us;
• the development of new competitive technologies and products;
• our ability to predict accurately the demand for our products, and products under development and to develop strategies to
•
address markets successfully;
• continued demand for our COVID-19 assays;
•
the timing, scope and effect of further U.S. and international governmental, regulatory, fiscal, monetary and public health
responses to the COVID-19 pandemic and any future public health crises;
• potential cybersecurity threats and targeted computer crime;
•
•
•
the ability to execute acquisitions and the impact and anticipated benefits of completed acquisitions and acquisitions we
may complete in the future;
the ability to consolidate certain of our manufacturing and other operations on a timely basis and within budget, without
disrupting our business and to achieve anticipated cost synergies related to such actions;
the ability to successfully manage ongoing organizational and strategic changes, including our ability to attract, motivate
and retain key employees and maintain engagement and efficiency in remote work environments;
• our ability to obtain regulatory approvals and clearances for our products, including the implementation of the European
Union Medical Device Regulations, and maintain compliance with complex and evolving regulations;
•
•
•
•
the coverage and reimbursement decisions of third-party payors;
the uncertainty of the impact of cost containment efforts and federal healthcare reform legislation on our business and
results of operations;
the guidelines, recommendations, and studies published by various organizations relating to the use of our products;
the effect of consolidation in the healthcare industry;
• our ability to meet production and delivery schedules for our products;
• our ability to protect our intellectual property rights;
•
•
•
the possibility that products may contain undetected errors or defects or otherwise not perform as anticipated;
the anticipated development of markets we sell our products into and the success of our products in these markets;
the anticipated performance and benefits of our products;
• business strategies;
• anticipated trends relating to our financial condition or results of operations, including the impact of interest rate and
foreign currency exchange fluctuations;
• estimated asset and liability values;
•
the impact of future tax legislation;
• conducting business internationally;
•
the impact and costs and expenses of any litigation we may be subject to now or in the future;
• our compliance with covenants contained in our debt agreements; and
• our liquidity, capital resources and the adequacy thereof.
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In some cases, you can identify forward-looking statements by terms such as “may,” “will,” “should,” “could,” “would,”
“expects,” “plans,” "intends," “anticipates,” “believes,” “estimates,” “projects,” “predicts,” "likely," "future," "strategy,"
“potential,” "seeks," "goal" and similar expressions intended to identify forward-looking statements. These statements are only
predictions and involve known and unknown risks, uncertainties, and other factors that may cause our actual results, levels of
activity, performance, or achievements to be materially different from any future results, levels of activity, performance, or
achievements expressed or implied by such forward-looking statements. Given these uncertainties, you should not place undue
reliance on these forward-looking statements. Also, these forward-looking statements represent our estimates and assumptions
only as of the date of this report. Except as otherwise required by law, we expressly disclaim any obligation or undertaking to
release publicly any updates or revisions to any forward-looking statement contained in this report to reflect any change in our
expectations or any change in events, conditions or circumstances on which any of our forward-looking statements are based.
Factors that could cause or contribute to differences in our future financial results include the cautionary statements set forth
herein and in our other filings with the Securities and Exchange Commission, including those set forth under “Risk Factors” set
forth in Part I, Item 1A of this Annual Report on Form 10-K (this "Annual Report"). We qualify all of our forward-looking
statements by these cautionary statements.
TRADEMARK NOTICE
Hologic is a trademark of Hologic, Inc. Other trademarks, logos, and slogans registered or used by Hologic and its
divisions and subsidiaries in the United States and other countries include, but are not limited to, the following: 3Dimensions,
3D Mammography, 3D, 3DQuorum, Acessa, Acessa ProVu, Aixplorer, Affirm, Amplidiag, Aptima, ATEC, BioZorb, Brevera,
Celero, Hologic Clarity HD, CoolSeal, C-View, Definity, DirectRay, Eviva, Faxitron, Fluent, Fluoroscan, Focal Therapeutics,
Genius 3D, Genius, Genius AI, Hologic, Horizon, InSight, Intelligent 2D, ImageChecker, JustRight, LOCalizer, MyoSure,
NovaSure, Novodiag, Panther, Panther Fusion, Progensa, Quantra, Rapid Ffn, SecurViewDX, Selenia, Selenia Dimensions,
Sertera, SmartCurve, Smart-Depth, SuperSonic Imagine, ThinPrep, Tigris, Tomcat, and UltraFast.
All other brand names or trademarks appearing in this Annual Report are the property of their respective owners.
Hologic’s use or display of other parties’ trademarks, trade dress or products in this Annual Report does not imply that Hologic
has a relationship with, or endorsement or sponsorship of, the trademark or trade dress owners.
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Item 1. Business
Overview
PART I
We are a developer, manufacturer and supplier of premium diagnostics products, medical imaging systems, and surgical
products focused on women's health and well-being through early detection and treatment. We sell and service our products
through a combination of direct sales and service personnel and a network of independent distributors and sales representatives.
We operate in four segments: Diagnostics, Breast Health, GYN Surgical and Skeletal Health. Until December 30, 2019, our
product portfolio included aesthetic and medical treatment systems sold by our former Medical Aesthetics business. We
completed the sale of our Medical Aesthetics segment on December 30, 2019 (the first day of the second quarter of fiscal
2020).
Through our Diagnostics segment, we offer a wide range of diagnostic products, which are used primarily to aid in the
screening and diagnosis of human diseases. Our primary Diagnostics products include our molecular diagnostic assays, which
run on our advanced instrumentation systems (Panther, Panther Fusion and Tigris), our ThinPrep cytology system, and the
Rapid Fetal Fibronectin Test. Our Aptima family of molecular diagnostic assays is used to detect, among other things, the
infectious microorganisms that cause common sexually transmitted diseases, or STDs, such as chlamydia and gonorrhea, or
CTGC; certain high-risk strains of human papillomavirus, or HPV; Trichomonas vaginalis, the parasite that causes
trichomoniasis; Mycoplasma genitalium; and Herpes Simplex viruses 1 and 2. We also offer viral load tests for the quantitation
of Hepatitis B virus, Hepatitis C virus, human immunodeficiency virus, or HIV-1, and human cytomegalo virus, or CMV, for
use on our Panther instrument system. In addition, we offer bacterial vaginosis and candida vaginitis assays for the diagnosis of
vaginitis, a common and complex ailment affecting millions of women a year. Our assay portfolio also includes diagnostic tests
for a range of acute respiratory infections, including SARS-CoV-2, various strains of influenza and parainfluenza, and
respiratory syncytial virus that are run on the Panther Fusion system, a field upgradeable instrument addition to the base Panther
system. In response to the COVID-19 pandemic, we developed and launched the Aptima SARS-CoV-2 assay and the Aptima
SARS-CoV-2/Flu assay (each of which runs on our standard Panther system) and the Panther Fusion SARS-CoV-2 assay
(which runs on our Panther Fusion system). In May 2022, we CE-marked two new molecular assays, Panther Fusion EBV
Quant assay for quantitation of Epstein-Barr virus, and the Panther Fusion BKV Quant assay for quantitation of the BK virus.
These two new assays are the first quantitative real-time PCR assays on the Panther Fusion system. These assays, along with
the Aptima CMV Quant assay already available in Europe, expand our Panther Fusion menu of transplant monitoring assays.
The ThinPrep System is primarily used in cytology applications, such as cervical cancer screening, and the Rapid Fetal
Fibronectin Test assists physicians in assessing the risk of pre-term birth. We also generate service revenues from our CLIA-
certified laboratory for testing related to breast cancer and all metastatic cancers.
Our Breast Health segment offers a broad portfolio of solutions for breast cancer care primarily in the areas of radiology,
breast surgery, pathology and treatment. These solutions include 3D digital mammography systems, image analytics software
utilizing artificial intelligence, reading workstations, ultrasound imaging, minimally invasive breast biopsy guidance systems,
breast biopsy site markers, localization, specimen radiology, connectivity solutions and breast conserving surgery products. Our
most advanced breast imaging platforms, Selenia Dimensions and 3Dimensions, utilize tomosynthesis to produce 3D images
that show multiple contiguous slice images of the breast, which we refer to as the Genius 3D Mammography exam.
Our GYN Surgical products include our NovaSure endometrial ablation system, or NovaSure, our MyoSure hysteroscopic
tissue removal system, or MyoSure, our Fluent fluid management system, or Fluent, our Acessa ProVu laparoscopic
radiofrequency ablation system, or Acessa, as well as our CoolSeal vessel sealing portfolio and our JustRight surgical stapler.
The NovaSure portfolio is comprised of the NovaSure CLASSIC device, NovaSure ADVANCED device and the NovaSure V5
device for the treatment of abnormal uterine bleeding. The MyoSure suite of devices offers four options to provide incision-less
removal of fibroids, polyps, and other pathology within the uterus. The Fluent system is a fluid management system that
provides liquid distention during diagnostic and operative hysteroscopic procedures. The Acessa system is a fully integrated
system that uses laparoscopic ultrasound, guidance mapping and radiofrequency ablation to treat nearly all types of fibroids.
The CoolSeal portfolio includes the Trinity, Reveal, and Mini advanced bipolar vessel sealing devices. The JustRight 5 mm
stapler features a smaller instrument profile and is used for laparoscopic general and pediatric surgery.
Our Skeletal Health segment's products include the Horizon DXA, a dual energy x-ray system, which evaluates bone
density and performs body composition assessments, and the Fluoroscan Insight FD mini C-arm, which assists in performing
minimally invasive orthopedic surgical procedures on a patient's extremities, such as the hand, wrist, knee, foot, and ankle.
Unless the context otherwise requires, references to we, us, Hologic or the Company refer to Hologic, Inc. and its
consolidated subsidiaries.
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Available Information
Our internet website address is www.hologic.com. Through our website, we make available, free of charge, our annual
report on Form 10-K, quarterly reports on Form 10-Q, current reports on Form 8-K and any amendments to those reports, as
well as proxy statements, and, from time to time, other documents as soon as reasonably practicable after we electronically file
such material with, or furnish it to, the Securities and Exchange Commission (SEC). These SEC reports can be accessed
through the investor relations section of our website. The information found on our website is not part of this or any other report
we file with or furnish to the SEC.
Investors and others should note that we announce material financial information to our investors using our investor
relations website (investors.hologic.com), SEC filings, press releases, public conference calls and webcasts. We use these
channels as well as social media to communicate with our members and the public about our Company, our services and other
issues. It is possible that the information we post on social media could be deemed to be material information. Therefore, we
encourage investors, the media, and others interested in our Company to review the information we post on the social media
channels listed on our investor relations website. We have used, and intend to continue to use, our investor relations website, as
well as our Twitter account (@Hologic), as means of disclosing material non-public information and for complying with our
disclosure obligations under Regulation FD. Additional corporate governance information, including our certificate of
incorporation, bylaws, governance guidelines, board committee charters, and code of business conduct and ethics, is also
available on our investor relations website under the heading “Governance.” The contents of our websites are not intended to be
incorporated by reference into this Annual Report or in any other report or document we file with the SEC, and any references
to our websites are intended to be inactive textual references only.
The SEC maintains an internet website that contains reports, proxy and information statements, and other information
regarding Hologic and other issuers that file electronically with the SEC. The SEC’s internet website address is www.sec.gov.
Products
We view our operations and manage our current business in four principal reporting segments: Diagnostics, Breast Health,
GYN Surgical and Skeletal Health. Financial information concerning these segments is provided in Note 16 to our audited
consolidated financial statements contained in Item 15 of this Annual Report. The following describes our principal products in
each of our segments.
Diagnostics Product Offerings
Molecular Diagnostic Assay Portfolio
Aptima Family of Molecular Diagnostic Assays. Our Aptima molecular diagnostic assays are used to detect, among other
things, the infectious microorganisms that cause common sexually transmitted diseases, or STDs, such as chlamydia and
gonorrhea, or CTGC; certain high-risk strains of human papillomavirus, or HPV; Trichomonas vaginalis, the parasite that
causes trichomoniasis; Mycoplasma genitalium; and Herpes simplex viruses 1 and 2. In addition, we also offer viral load assays
for the quantitation of Hepatitis B virus, or HBV, Hepatitis C virus, or HCV, human immunodeficiency virus, or HIV-1, and
human cytomegalovirus, or CMV, for use on our Panther instrument system. All four of these viral load assays are both CE-
marked and FDA approved. We also offer our Aptima BV and Aptima CV/TV assays for the diagnosis of vaginitis, a common
and complex ailment affecting millions of women a year. In response to the COVID-19 pandemic, we developed and launched
our Aptima SARS-CoV-2 assay for the detection of SARS-CoV-2, the virus that causes COVID-19 disease, and our Aptima
SARS-CoV-2/flu assay for the detection and differentiation of SARS-CoV-2, influenza A and influenza B, each of which runs
on our standard Panther system. Both of these assays have been granted Emergency Use Authorization by the FDA and are also
CE-marked. Our Aptima products integrate a number of proprietary core technologies, including our target capture technology,
our Transcription Mediated Amplification, or TMA, technology, and our hybridization protection assay, or HPA, and dual
kinetic assay, or DKA, technologies, to produce highly sensitive amplification assays. Each of these technologies is described
in greater detail below.
Target Capture/Nucleic Acid Extraction Technology. The detection of target organisms that are present in small numbers
in a large-volume clinical sample requires that target organisms be concentrated to a detectable level. One way to accomplish
this is to isolate the particular nucleic acid of interest by binding it to a solid support. This support, with the target bound to it,
can then be separated from the original sample. We refer to such techniques as “target capture.” We have developed target
capture techniques to immobilize nucleic acids on magnetic beads by using a “capture probe” that binds to the bead and to the
target nucleic acid. We use magnetic separation to concentrate the target by drawing the magnetic beads to the sides of a sample
tube, while the remainder of the sample is removed from the tube. When used in conjunction with our amplification procedures,
target capture techniques concentrate the nucleic acid target(s) and also remove materials in the sample that might otherwise
interfere with amplification.
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Transcription-Mediated Amplification (TMA) Technology. The goal of amplification technologies is to increase the copy
number of a target nucleic acid sequences that may be present in samples in small numbers. These copies can then be detected
using nucleic acid probes. Amplification technologies can yield results in only a few hours versus the several days or weeks
required for traditional culture methods. TMA is a transcription-based amplification system that uses two different enzymes to
drive the process. The first enzyme is a reverse transcriptase that creates a double-stranded DNA copy from an RNA or DNA
template. The second enzyme, an RNA polymerase, makes thousands of copies of the complementary RNA sequence, known
as the “RNA amplicon,” from the double-stranded DNA template. Each RNA amplicon serves as a new target for the reverse
transcriptase and the process repeats automatically, resulting in an exponential amplification of the original target that can
produce over a billion copies of the RNA amplicon in less than thirty minutes.
Hybridization Protection Assay (HPA) and Dual Kinetic Assay (DKA) Technologies. With our HPA technology, we have
simplified testing, further increased test sensitivity and specificity, and increased convenience. In the HPA process, the
acridinium ester, or AE, molecule is protected within the double-stranded helix that is formed when the probe binds to its
specific target. Prior to activating the AE molecule, known as “lighting off,” a chemical is added that destroys the AE molecule
on any unhybridized probes, leaving the label on the hybridized probes largely unaffected. When the “lighting off” or detection
reagent is added to the specimen, only the label attached to the hybridized probe is left to produce a signal indicating that the
target organism’s DNA or RNA is present. All of these steps occur in a single tube and without any wash steps, which were
required as part of conventional probe tests. Our DKA technology uses two types of AE molecules that can be differentiated
from each other — one that “flashes” and another one that “glows.” By using DKA technology, we have created nucleic acid
test, or NAT, assays that can detect two separate targets simultaneously.
Panther Fusion Family of Molecular Diagnostic Assays. The Panther Fusion molecular diagnostic assays are performed
on the Panther Fusion system and utilize polymerase chain reaction, or PCR, technology to amplify target nucleic acid
sequences for easier detection. Our Panther Fusion assay portfolio includes diagnostic tests for a range of acute respiratory
infections (influenza A virus, influenza B virus, respiratory syncytial virus, adenovirus, human metapneumovirus, rhinovirus
and parainfluenza). In addition, in response to the COVID-19 pandemic, in fiscal 2020 we developed and launched the Panther
Fusion SARS-CoV-2 assay for the detection of SARS-CoV-2. The Panther Fusion SARS-CoV-2 assay was granted Emergency
Use Authorization by the FDA in March 2020. In countries recognizing the CE-mark, we also offer the Panther Fusion SARS-
CoV-2/Flu A/B/RSV assay for the detection and differentiation of SARS-CoV-2, influenza A, influenza B and respiratory
syncytial virus, or RSV, the Panther Fusion EBV Quant assay for quantitation of Epstein-Barr virus, the Panther Fusion BKV
Quant assay for quantitation of the BK virus, the Panther Fusion MRSA assay for detection and differentiation of
Staphylococcus aureus and methicillin-resistant Staphylococcus aureus, and the Panther Fusion Bordetella assay for the
detection and differentiation of Bordetella pertussis and Bordetella parapertussis infections.
Molecular Diagnostic Instrumentation
We have developed and continue to develop instrumentation and software designed specifically for use with certain of our
molecular diagnostic assays. We also provide technical support and service to maintain these instrument systems in the field.
By placing our proprietary instrumentation in laboratories and hospitals, we can establish a platform for future sales of our
assays.
Our instrumentation includes the Tigris system, an integrated, fully-automated testing instrument for high-volume
laboratories which is approved for use with certain of our Aptima assays; the Panther instrument system, an integrated, fully-
automated testing instrument capable of serving high-, medium- and low-volume laboratories; and our semi-automated direct
tube sampling, or DTS, instruments which are used to run a number of infectious disease assays. Our instrumentation also
includes the Tomcat instrument, a fully automated general-purpose instrument designed to improve pre-analytical sample
processing by eliminating the inefficient and error-prone activities associated with manually transferring samples from one tube
to another. In addition, our Panther Fusion system, including the related Fusion assays for flu and respiratory testing, extends
the capabilities of our Panther system by adding the flexibility of PCR, functionality to our existing TMA-based technology.
The Panther Fusion system is available as a modular in-lab upgrade to our base Panther system.
ThinPrep System
The ThinPrep System is the most widely used method for cervical cancer screening in the U.S. The ThinPrep System has
multiple configurations, including one or more of the following: the ThinPrep 2000 Processor, ThinPrep 5000 Processor,
ThinPrep5000 Processor with Autoloader, ThinPrep Genesis Processor, ThinPrep Imaging System, ThinPrep Integrated Imager,
and related reagents, filters and other supplies, such as the ThinPrep Pap Test and our ThinPrep PreservCyt Solution.
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The ThinPrep Process. The ThinPrep process begins with the patient’s cervical sample being obtained by the physician
using a cervical sampling device that, rather than being smeared on a microscope slide as in a conventional Pap smear, is
inserted into a vial filled with our proprietary ThinPrep PreservCyt Solution. This enables most of the patient’s cell samples to
be preserved before the cells can be damaged by air drying. The ThinPrep specimen vial is then labeled and sent to a laboratory
equipped with a ThinPrep Processor for slide preparation. At the laboratory, the ThinPrep specimen vial is inserted into a
ThinPrep Processor, a proprietary sample preparation device, which automates the process of preparing cervical slides for
staining and microscopic examination. Additionally, an aliquot used for subsequent molecular testing can be produced using the
ThinPrep Genesis Processor.
In the case of manual screening, the cytotechnologist screens each Pap test slide with a microscope to first determine the
adequacy of the slide and then to examine the entire slide to differentiate diseased or abnormal cells from normal cells. With the
ThinPrep Imaging Systems, the screening process has been automated to combine the power of computer imaging technology
with human interpretive skills. Prior to human review, the ThinPrep Imaging Systems rapidly scan, locate and highlight areas of
interest for review. By directing the cytotechnologist to areas of interest on a slide, these systems may increase a cytology
laboratory’s screening productivity and diagnostic accuracy.
Additional Applications. In addition to serving as a replacement for the conventional Pap smear, the ThinPrep System can
also be used for non-gynecological cytology screening applications including fine-needle aspiration specimens (e.g., breast,
thyroid, lung or liver), body fluids (e.g., urine, pleural fluid, ascitic fluid or pericardial fluid), respiratory specimens (e.g.,
sputum or brushing of respiratory tracts) and ancillary testing (e.g., cell blocks, immunocytochemistry or special stains).
Genius Digital Diagnostics
The Genius Digital Diagnostics System is the first CE-marked digital cytology platform to combine a new artificial
intelligence, or AI, algorithm with advanced volumetric imaging technology to help cytotechnologists and pathologists identify
pre-cancerous lesions and cervical cancer cells in women. The Genius Digital Diagnostics System consists of an advanced
digital imager featuring volumetric imaging technology, a secure image management server to store images, a deep learning-
based AI algorithm that is designed to assist healthcare providers in detecting pre-cancerous lesions and cervical cancer cells,
and a high-resolution review station for local or remote case review. The Genius Digital Diagnostics System can rapidly
analyze all cells on a ThinPrep Pap test digital image, narrowing tens of thousands of cells down to an AI-generated gallery of
images that have been selected as the most diagnostically relevant images, which gives healthcare providers additional critical
information to help guide earlier detection and make better treatment decisions for patients. The Genius Digital Diagnostics
System was CE-marked for diagnostic use in November 2020, and we have submitted a De Novo request to the FDA to grant
class II marketing authorization for the product in the U.S.
Rapid Fetal Fibronectin Test
The Rapid Fetal Fibronectin Test is a single-use disposable test used to determine a woman’s risk of pre-term birth by
detecting the presence of a specific protein, fetal fibronectin, in vaginal secretions during pregnancy. The test utilizes a single-
use, disposable cassette and is analyzed on our instrument, the TLi IQ System.
Oncology Product Offerings
In February 2021, we completed the acquisition of Biotheranostics, Inc., or Biotheranostics, and now offer two proprietary
laboratory developed tests, or LDTs, that support physicians in the treatment of cancer: the Breast Cancer Index test and the
CancerTYPE ID test. The Breast Cancer Index, or BCI, test is a PCR-based gene expression test used for determining which
patients with early-stage, hormone-receptor positive, or HR+, breast cancer are likely to benefit from extended endocrine
therapy. In January 2021, the National Comprehensive Cancer Network revised its clinical practice guidelines to include BCI as
the only gene expression assay to predict benefit from extended endocrine therapy for patients with early-stage HR+ breast
cancer. In addition, in April 2022 the American Society of Clinical Oncology updated its clinical practice guidelines, which
now include BCI as the only genomic test to help guide extended endocrine therapy decisions in early-stage, HR+ breast cancer
patients. The CancerTYPE ID test is a PCR-based gene expression test that is designed to identify the source of metastatic
cancer in order to improve diagnostic accuracy and inform treatment decisions. Both of these LDTs are offered as a service
solely out of Biotheranostics' licensed, CLIA-certified, CAP-accredited laboratory in San Diego, California.
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Mobidiag Product Offerings
In June 2021, we completed the acquisition of Mobidiag Oy, or Mobidiag, a developer of innovative molecular diagnostic
tests and instrumentation, headquartered in Espoo, Finland. Mobidiag develops and markets PCR-based tests for acute care
conditions such as gastrointestinal and respiratory infections (including SARS-CoV-2), antimicrobial resistance management,
and healthcare associated infections. The Amplidiag and Novodiag platforms are automated instruments that deliver rapid
turnaround times ranging from 50 minutes to two hours. The Novodiag instrument combines real-time PCR and microarray
capabilities to provide high level multiplexing, assisting clinicians in efficiently identifying which organism is responsible for
an infection. Although Mobidiag currently does not offer any of its products in the U.S., we intend to invest in assay
development to drive growth of the Novodiag instrument, including seeking clearance for the Novodiag instrument and related
assays in the U.S.
Breast Health Products
Mammography Solutions
Our Dimensions platform includes the Selenia Dimensions and 3Dimensions systems capable of performing both 2D and
3D tomosynthesis image acquisition and display. When operating in tomosynthesis mode, each system acquires a series of low
dose x-ray images taken in a scanning motion at various angles. The images are mathematically processed into a series of small
slices, allowing for visualization of the breast in multiple contiguous slices. Our clinical results for FDA approval demonstrated
that conventional 2D digital mammography with the addition of our Genius 3D Mammography is superior to 2D digital
mammography alone for both screening and diagnostics. Hologic Clarity HD technology provides our highest resolution
imaging, and our C-View and Intelligent 2D software products provide 2D images that are mathematically synthesized from the
data within a tomosynthesis exam. Elimination of the 2D exposure reduces the breast compression time and patient dose
compared to the current "combo" exam, which includes a tomosynthesis exam and a conventional digital 2D exam.
Our 3DQuorum technology, powered by Genius AI, is an artificial intelligence, or AI, powered algorithm that expedites
mammography exam reading time without compromising image quality, sensitivity or accuracy. The 3DQuorum technology
uses Genius AI-powered analytics to uniquely reconstruct high-resolution 3D data to produce 6 mm “SmartSlices.” By utilizing
3DQuorum technology the number of 3D images to review is reduced by two-thirds, saving an estimated average of one hour
per eight hours of daily image interpretation time. The 3DQuorum technology also reduces the typical Hologic Clarity HD and
Intelligent 2D study size by approximately 50%, bringing the storage space and network impact back down to that of standard
resolution 3D imaging.
The images captured by digital mammography systems are typically transmitted electronically for review by a radiologist
at a reading workstation. To address this process, we offer the SecurViewDX workstation approved for interpretation of
mammograms from most vendors as well as images from other diagnostic breast modalities. We also offer image analytic
products such as Genius AI Detection (Hologic's first artificial intelligence cancer detection algorithm utilizing deep-learning
technology) and ImageChecker CAD to provide markings of suspicious areas of the breast that may be cancerous, as well as
Quantra software to automate breast density measurement tools for our mammography systems. These technologies provide
reviewers with the potential to focus on key patients that might otherwise be overlooked during the review process, thus
potentially increasing cancer detection.
Stereotactic Breast Biopsy Systems
We provide clinicians with the flexibility of choosing prone or upright systems for breast biopsy by offering two
minimally invasive stereotactic breast biopsy guidance systems: the Affirm Prone breast biopsy table and the Affirm upright
system. The Affirm upright attachment is used with our Dimensions systems. These breast biopsy systems provide an
alternative to open surgical biopsy and can be performed as an outpatient procedure under local anesthesia, allowing shorter
recovery times. The Affirm tomosynthesis option provides faster lesion targeting and reduced patient procedure time compared
to traditional stereotactic biopsy procedures. The Affirm system is pre-programmed for use with our Brevera, Eviva and ATEC
vacuum-assisted breast biopsy devices.
Ultrasound Solutions
Ultrasound is used extensively by clinicians across the breast health continuum including screening, diagnosis,
interventions, and surgical treatments. Ultrasound is commonly used as a complement to 3D mammography screening for
women with dense breast tissue, as a diagnostic tool to further characterize lesions prior to biopsy, and for interventional and
surgical guidance. Our UltraFast technology enables innovative imaging modes and frame rates of up to 20,000 images per
second resulting in high performance and image quality. Our portfolio consists of premium ultrasound carts including the
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Aixplorer, Mach 20, Mach 30, and Mach 40 ultrasound system. The Supersonic Mach 40 ultrasound systems offers integration
benefits with our existing breast health portfolio.
Breast Biopsy and Surgery Products
We offer a wide range of minimally invasive products for breast biopsy and breast surgery. Our breast biopsy portfolio
includes three types of tethered vacuum-assisted breast biopsy products; the Brevera, ATEC, and Eviva devices. Each tethered
device is powered by a console and utilizes our fluid management system. The ATEC device can be used under all standard
imaging guidance modalities (stereotactic x-ray, ultrasound, MRI and molecular breast imaging) whereas our Brevera and
Eviva devices are used exclusively under stereotactic x-ray guidance. We also offer the Celero and Sertera biopsy devices, both
of which are non-tethered (no separate console), spring-loaded, disposable core biopsy devices, which are used exclusively
under ultrasound-guidance. We also have products for marking, localizing and filling the void after surgery in addition to
specimen imaging products for radiology, surgery and pathology.
GYN Surgical Products
NovaSure
The NovaSure CLASSIC endometrial ablation system allows physicians to treat women suffering from abnormal uterine
bleeding. The system features Smart-Depth technology that continuously monitors and measures tissue impedance to provide a
more customized, reliable and reproducible depth of ablation for every patient. The NovaSure system consists of a disposable
device and a controller that delivers RF energy to ablate the endometrial lining of the uterus in order to eliminate or reduce the
patient’s abnormal bleeding. The NovaSure disposable device is a hand-held, single-use device that incorporates a flexible
gold-plated mesh electrode used to deliver the RF energy to the endometrial tissue. The NovaSure RF Controller generates and
delivers RF energy customized for each patient, monitors several critical treatment and safety parameters, and automatically
controls the endpoint of the procedure. We also offer the NovaSure ADVANCED and NovaSure V5 devices, which have a
slimmer diameter. These devices are designed to improve patient comfort and physician ease-of-use while maintaining the
clinical efficacy of the NovaSure system.
MyoSure
The MyoSure system is designed to provide efficient and effective hysteroscopic removal of tissue within the uterus,
including fibroids and polyps. Removal of fibroids can provide effective relief from heavy menstrual bleeding commonly
attributed to such pathology. Unlike other methods of tissue removal, the excavated tissue samples remain intact, which allows
them to be tested for abnormalities. The MyoSure system consists of a tissue removal device, control unit, and hysteroscope.
The MyoSure tissue removal device is single-use and features simultaneous tissue cutting and removal. The device incorporates
a rapidly rotating and reciprocating cutting blade. During the procedure, the tissue removal device is inserted through the
MyoSure hysteroscope. This tissue removal device is powered by a control unit, which features a simple user interface and is
foot pedal activated. We offer multiple handpiece devices that differ in size and are focused on addressing different pathology
types.
Fluent Fluid Management System
Our Fluent Fluid Management System is utilized for diagnostic and operative hysteroscopic procedures. Fluent is
designed for simplified setup and operation, and streamlined workflow for the operating room team.
Acessa ProVu System
The Acessa ProVu System is used by laparoscopic surgeons to treat fibroids using controlled radiofrequency energy (heat)
to cause coagulative necrosis. The treated tissue softens and shrinks over time, allowing fibroid symptoms to resolve without
more invasive treatment. The Acessa System includes an ultrasound probe to locate the fibroids, guidance mapping that
provides visual cues, and a percutaneous handpiece that deploys radiofrequency energy.
Advanced Energy and Surgical Stapling
The CoolSeal vessel sealing suite and JustRight surgical stapler bolster our laparoscopic surgical offerings with its
advanced vessel sealing, dividing, dissection, and stapling tools. The CoolSeal device allows for dissection, vessel sealing and
dividing all in one tool. The ability to use a combination device improves surgical efficiency by reducing the need for
instrument exchanges. In addition, the CoolSeal Mini 3 mm sealer and the JustRight 5 mm stapler are designed for small
surgical spaces such as in pediatric cases, which can help reduce the need for larger, overpowered instruments.
Skeletal Health Products
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Horizon DXA Systems
Bone densitometry is the measurement of bone density to assist in the diagnosis and monitoring of osteoporosis and other
metabolic bone diseases that can lead to frailty and debilitating bone fractures. Osteoporosis is a disease that is most prevalent
in post-menopausal women. Our Horizon line of x-ray bone densitometers incorporates advanced features designed for bone
health screening and body composition assessment. Body composition assessment is the precise measurement of bone, lean
mass, and fat mass within the body. These measurements are valued within the health and wellness and human performance
categories, informing nutrition and exercise programming decisions.
Fluoroscan Insight FD
Our Fluoroscan Insight FD is a mini C-arm imaging system that provides low intensity, real-time x-ray imaging, with
high-resolution images at radiation levels and at a cost below those of conventional x-ray and standard sized fluoroscopic
equipment. Mini C-arm systems are used primarily by orthopedic surgeons to assist in performing minimally invasive surgical
procedures on a patient’s extremities, such as the hand, wrist, knee, foot and ankle.
Marketing, Sales and Service
We sell and service our products through a combination of direct sales and service forces and a network of independent
distributors and sales representatives. In fiscal 2022, 2021, and 2020, no customer accounted for more than 10% of our
consolidated revenues. In fiscal 2020, revenues from two customers accounted for 12.5% and 10.9%, respectively, of our
Diagnostics segment revenue. These customers were large clinical laboratories reflecting the consolidation in that industry. No
other customer accounted for more than 10% of our revenues in any other business segment in fiscal 2022, 2021, or 2020.
Our U.S. sales force is structured to specifically target the customers in each of our business segments. We maintain
distinct teams focused on the Diagnostics, Breast Health, GYN Surgical, and Skeletal Health markets. Our end customers
include clinical laboratories, hospitals, healthcare providers and surgeons in both hospital and office settings, and we target
various specialists at healthcare entities who use our products, such as ob-gyns, radiologists and breast surgeons.
A critical element of our strategy in the U.S. for our Diagnostics, Breast and Skeletal Health, and GYN Surgical divisions
has been to utilize the results of our clinical trials and expanded FDA labeling to demonstrate safety, efficacy and productivity
improvements to our target customers. Our U.S. sales efforts also include the use of national account managers focused on
obtaining purchasing contracts from large purchasing entities, such as managed care organizations, integrated delivery networks
and government healthcare facilities. In addition, in certain regions of the U.S., we use a limited number of independent dealers
or distributors to sell and service certain of our products. Internationally, our products in all divisions are marketed and sold
through a combination of a direct sales force and a network of distributors.
Our service organization is responsible for installing our products and providing warranty and repair services,
applications training and biomedical training. Products sold by our direct sales force typically carry limited warranties covering
parts and labor for twelve months. Products sold through dealers also carry limited warranties that are typically for twelve
months and cover only parts and components. We also offer service contracts that generally cover one to three years after the
original warranty period. We provide both repair services and routine maintenance services under these arrangements, and also
offer repair and maintenance services on a time and materials basis to customers that do not have service contracts. Our Breast
Health business generates a majority of our service revenue, primarily relating to service contracts for our digital
mammography and related products. Internationally, we primarily use distributors, sales representatives and third parties to
provide maintenance service for our products, however we do provide direct service in countries where we have a subsidiary
(Germany, UK, France, Spain, Japan, China, and Australia).
Competition
The healthcare industry is highly competitive and characterized by continual change and improvements in technology.
This is particularly the case in the market segments in which we operate. A number of companies have developed or are
expected to develop products that compete or will compete with our products. Many of these competitors offer a broader
product portfolio and have greater brand recognition than we do, which may make these competitors more attractive to
hospitals, radiology clients, group purchasing organizations, laboratories, physicians and other potential customers. Competitors
may develop superior products or products of similar quality for sale at the same or lower prices. Moreover, our products could
be rendered obsolete by changes to industry standards or guidelines or advances in technology. We can give no assurance that
we will be able to compete successfully with existing or new competitors.
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In the current environment of managed care, economically motivated buyers, consolidation among healthcare providers,
increased competition and declining reimbursement rates, we have been increasingly required to compete on the basis of price,
value, reliability and efficiency. We believe the current global economic conditions and healthcare reform measures are putting
additional competitive pressure on us, including on our average selling prices, overall procedure rates and market sizes.
We believe that the success of our products depends on our ability to differentiate ourselves and to demonstrate that our
products deliver the clinical and operational attributes that are most important and cost-effective to customers. These attributes
include, but are not limited to, superiority in efficacy, ease of use, reliability, accuracy, quality and cost. We believe our
continued success depends in large part upon our ability to invest in product enhancements and technologies that will help us
distinguish ourselves from our competitors.
Diagnostics. Our ThinPrep liquid-based cytology product faces direct competition in the U.S. primarily from Becton,
Dickinson and Company, or BD, which manufactures a competitive offering. We also compete with the conventional Pap smear
and other alternative methods for detecting cervical cancer and/or its precursors. Internationally, our ThinPrep product
competes with a variety of companies and other non-FDA approved tests, since the devices often have lower risk classification
with fewer regulatory barriers in many international markets as compared to the U.S. Additionally, testing volume in this
category is also under pressure due to clinical guideline changes, which lengthen the interval between screenings and
increasingly afford the option of HPV testing as the primary means of detection.
We believe that our Rapid Fetal Fibronectin Test is currently the only available in vitro diagnostic test for predicting the
risk of pre-term birth in the U.S. Internationally, our Rapid Fetal Fibronectin Test competes with Actim Partus manufactured by
Medix Biochemica and PartoSure manufactured by Qiagen GmbH, or Qiagen. However, our Rapid Fetal Fibronectin Test could
also experience competition from companies that manufacture and market pregnancy-related diagnostic products and services.
In addition, healthcare providers use diagnostic techniques such as clinical examination and transvaginal ultrasound to help
diagnose the likelihood of pre-term birth and may use these techniques together with the Rapid Fetal Fibronectin Test or instead
of using the Rapid Fetal Fibronectin Test.
In the molecular diagnostics market, our products compete with many companies in the U.S. and abroad engaged in the
development, commercialization and distribution of similar products intended for clinical molecular diagnostic applications.
Clinical laboratories also may offer testing services that are competitive with our products and may use reagents purchased
from us or others to develop their own lab developed tests. The market for our COVID-19 assays is rapidly evolving both in the
United States and in the rest of the world. For example, in the United States over 400 assays have received Emergency Use
Authorization from the FDA, and we compete with the providers of all of these tests, including manufacturers of molecular
diagnostic tests (including so-called high throughput nucleic acid tests, rapid antigen tests and at-home testing solutions), and
antibody tests, as well clinical laboratories making their own lab developed tests for the detection of SARS-CoV-2.
In the global clinical diagnostics market, we compete with several companies offering alternative technologies to our
diagnostic products. For example, in the U.S., our Aptima Combo 2 test competes against Abbott Laboratories, BD, Danaher
Corporation (through its acquisition of Cephaid), and Roche Diagnostics Corporation, or Roche, and our Aptima HPV test
competes with tests marketed by BD, Qiagen and Roche.
Breast Health. Our mammography and related products and subsystems compete on a worldwide basis with products
offered by a number of competitors, including General Electric Company, or GE, Siemens AG, or Siemens, Koninklijke Philips
NV, or Philips, Planmed Oy, or Planmed, Carestream Health, Inc., or Carestream, FUJIFILM Holdings Corporation, or Fuji,
Internazionale Medico Scientifica Srl, or I.M.S., and Toshiba Corporation. In the U.S., our digital mammography systems
compete with digital mammography systems from GE, Siemens, Fuji, I.M.S., Philips and Planmed. Our digital mammography
systems also compete with Fuji’s and Carestream's Computed Radiography, or CR mammography systems, and other lower-
priced alternatives to 2D digital mammography and analog mammography systems. In the U.S., GE, Siemens and Fuji have
received FDA approval for their breast tomosynthesis systems, and we believe that other competitors are developing
tomosynthesis systems for commercial use in the U.S. Our Dimensions tomosynthesis systems also compete in certain countries
outside of the U.S. with tomosynthesis systems developed by GE, Siemens, Fuji, and I.M.S.
The primary competitor for our breast biopsy product line is Devicor Medical Products, Inc., part of Danaher
Corporation's Leica Biosystems division. In addition, other competitors include CareFusion, a BD company and Intact Medical
Corporation.
GYN Surgical. Our NovaSure system currently faces direct competition from The Cooper Companies, Inc., or
CooperSurgical, and Minerva Surgical, Inc., or Minerva, each of which currently markets an FDA-approved endometrial
ablation device for the treatment of abnormal uterine bleeding. In addition to these devices, we also compete with alternative
treatments to our NovaSure system, such as drug therapy, intrauterine devices, hysterectomy, dilation and curettage and
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rollerball ablation. Because drug therapy is an alternative to our NovaSure procedure, NovaSure’s competitors also include
many major pharmaceutical companies that manufacture hormonal drugs for women.
Our MyoSure product competes directly with hysteroscopic loop resection, as well as hysteroscopic tissue removal
systems such as Medtronic plc’s TruClear device and Minerva's Symphion device. The MyoSure product also competes with
alternative therapeutic techniques such as hysteroscopic resection with a monopolar or bipolar loop, which is currently the most
common technique for removing intrauterine fibroids and polyps.
Our Acessa ProVu System competes directly with Gynesonics, Inc., which currently markets a radiofrequency ablation
device for treating uterine fibroids. The Acessa ProVu System also competes with alternative fibroid treatment options such as
hysterectomy, laparoscopic myomectomy, and uterine artery embolization.
Our CoolSeal vessel sealing suite competes directly with Applied Medical's Voyant vessel sealing, Medtronic's LigaSure
vessel sealing, Ethicon's ENSEAL vessel sealing and Olympus' THUNDERBEAT and POWERSEAL vessel dealing devices.
CoolSeal also competes with ultrasonic energy sealing procedures done by Medtronic's Sonicision and Ethicon's HARMONIC
sealing devices.
Skeletal Health. GE is our primary competitor in the bone densitometry market, and we also compete with Orthoscan Inc.
in the mini-C arm market.
Manufacturing
We purchase many of the components, subassemblies, and raw materials used in our products from numerous suppliers
worldwide. For reasons of quality assurance, scarcity and/or cost effectiveness, certain components, subassemblies, and raw
materials used in our products are available only from one or a limited number of suppliers. We work closely with our suppliers
to develop contingency plans to ensure continuity of quality and reliable supply. We have established long-term supply
contracts with many of our suppliers, and in other instances, we developed in-house capability to offset potential shortages
caused by sole source suppliers. Due to the high standards and FDA requirements applicable to manufacturing our products,
such as the FDA's Quality System Regulation and Good Manufacturing Practices, we may not be able to quickly establish
additional or replacement sources for certain components or materials. In addition, the COVID-19 pandemic and associated
economic disruptions have had an adverse impact on our supply chains. Moreover, we use certain components in our products,
including semiconductor chips, which have been the subject of recent global supply chain shortages and disruptions. In the
event we are unable to obtain sufficient quantities of raw materials or components or subassemblies on commercially
reasonable terms or in a timely manner, our ability to manufacture our products on a timely and cost-competitive basis may be
compromised, which may have a material adverse effect on our business, financial condition and results of operations. For
additional information about supply chain shortages and disruptions to which our business is subject, see the disclosures under
the caption “Supply Chain Considerations” in Item 7 of this Annual Report.
Our current supplier of certain key raw materials for certain of our amplified NAT diagnostic assays is Roche, a direct
competitor of our Diagnostics business. Our Diagnostics business has two supply agreements with GE Healthcare Bio-Sciences
Corp., an affiliate of GE, for membranes used in connection with our ThinPrep product line and for primers used in the
manufacture of certain of our molecular products. GE is a direct competitor with our Breast Health and Skeletal Health
businesses.
We have sole source third-party contract manufacturers for each of our molecular diagnostics instrument product lines
and for our Skeletal Health products. KMC Systems, Inc., or KMC Systems, is the only manufacturer of spare parts for our
Tigris instrument; Stratec SE, or Stratec, is the only manufacturer of the Panther and Panther Fusion instruments; and
Flextronics Medical Sales and Marketing, LTD, or Flextronics, is the only manufacturer of our Skeletal Health finished goods
products. We are dependent on these sole source third-party manufacturers, and this dependence exposes us to increased risks
associated with production delays, delivery schedules, manufacturing capability, quality control, quality assurance and costs.
We have no firm long-term volume commitments with either KMC Systems, Stratec or Flextronics. If KMC Systems, Stratec,
Flextronics or any of our other third-party manufacturers experiences delays, disruptions, capacity constraints or quality control
problems in its development or manufacturing operations, curtails operations or otherwise fails to supply us with products in
sufficient quantities, instrument and equipment shipments to our customers could be delayed or cancelled, which would
decrease our revenues and may harm our competitive position and reputation. Further, because we place orders with our
manufacturers based on forecasts of expected demand for our instruments and Skeletal Health products, if we inaccurately
forecast demand, we may be unable to obtain adequate manufacturing capacity or adequate quantities of components to meet
our customers' delivery requirements.
We, and our contract manufacturers, manufacture our products at a limited number of different facilities located in the
U.S. and throughout the world. In most cases, the manufacturing of each of our products is concentrated in one or a few
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locations. An interruption in manufacturing capabilities at any of these facilities, as a result of equipment failure or other
reasons, could reduce, delay or prevent the production of our products. Some of our manufacturing operations are located
outside of the U.S., including in Costa Rica and the United Kingdom. Those manufacturing operations are also subject to
additional challenges and risks associated with international operations described under the caption “Risk Factors” set forth in
Part I, Item 1A of this Annual Report.
From time-to-time new regulations are enacted that can affect the content and manufacturing of our products. We
evaluate the necessary steps for compliance with regulations as they are enacted. In August 2012, the SEC adopted a rule
requiring disclosures of specified minerals, known as conflict minerals, which are necessary to the functionality or production
of products manufactured or contracted to be manufactured by public companies. The conflict minerals rule requires companies
annually to disclose and report whether or not such minerals originate from the Democratic Republic of Congo or an adjoining
country. The conflict minerals rule could affect sourcing at competitive prices and availability in sufficient quantities of certain
minerals used in the manufacture of our products, including tantalum, tin, gold and tungsten. The number of suppliers who
provide conflict-free minerals may be limited. In addition, there may be material costs associated with complying with the
disclosure requirements, such as costs related to determining the source of certain minerals used in our products, as well as
costs of possible changes to products, processes, or sources of supply as a consequence of such verification activities. Since our
supply chain is complex, we may not be able to sufficiently verify the origins of the relevant minerals used in our products
through the due diligence procedures that we implement, which may harm our reputation. In addition, we may encounter
challenges to satisfy those customers who require that all of the components of our products be certified as conflict-free, which
could place us at a competitive disadvantage if we are unable to do so.
Other regulations which affect the content and manufacturing of our products include, for example, the Registration,
Evaluation, Authorization and Restriction of Chemical substances, or REACH, the Restriction on the Use of Certain Hazardous
Substances in Electrical and Electronic Equipment Directive, or RoHS, and the Waste Electrical and Electronic Equipment
Directive, or WEEE, enacted in the European Union which require the registration of and regulate the use of certain hazardous
substances and chemicals in, and require the collection, reuse and recycling of waste from, certain products we manufacture.
Similar legislation that has been or is in the process of being enacted in Japan and China and various states of the U.S. may
require us to re-design our products to ensure compliance with the applicable standards, for example by requiring the use of
different types of materials. These redesigns or alternative materials may detrimentally impact the performance of our products,
add greater testing lead-times for product introductions, result in additional costs or have other similar negative effects.
Research and Development
The markets in which we participate are characterized by rapid technological change, frequent product introductions and
evolving customer requirements. Investment in research and development is critical to driving our future growth. Our research
and development efforts are focused on the further development and improvement of our existing products, the design and
development of new innovative medical technologies and regulatory compliance across all our business segments. In fiscal
2020, in response to the COVID-19 pandemic, we developed and launched the Aptima SARS-CoV-2 assay (which runs on our
Panther system) and the Panther Fusion SARS-CoV-2 assay (which runs on our Panther Fusion system).
In addition to product development, our research and development personnel play an active role in the review of product
specifications, clinical protocols and FDA submissions, as well as ensuring that certain of our products conform to European
health, safety and environmental requirements, or CE-marking.
Patents and Proprietary Rights
We rely primarily on a combination of trade secrets, patents, copyrights, trademarks and confidentiality procedures to
protect our products and technology. Due to the rapid technological changes that characterize the markets we operate in, we
believe that trade secrets and other unpatented know-how relied upon in connection with the development of new products and
the enhancement of existing products are generally as important as patent protection in establishing and maintaining a
competitive advantage. Nevertheless, we have obtained patents and will continue to make efforts to obtain patents, when
available, in connection with our product development programs. We do not consider our business to be materially dependent
upon any individual patent.
We own numerous U.S. patents and have applied for numerous additional U.S. patents relating to our technologies. We
also own or have applied for corresponding patents in selected foreign countries. These patents relate to various aspects of most
of our products. We do not know if current or future patent applications will be issued with the full scope of the claims sought,
if at all, or whether any patents issued will be challenged or invalidated. There is a risk that our patent applications will not
result in granted patents or that granted patents will not provide significant protection for our products and technology. Third
parties may infringe, misappropriate or otherwise violate our intellectual property rights, or copy or reverse engineer portions of
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our technology. Our competitors may independently develop similar or superior technology that our patents do not cover. In
addition, because patent applications in the U.S. are not generally publicly disclosed until eighteen months after the application
is filed, unpublished applications may have been filed by third parties that relate to our technology. Moreover, there is a risk
that foreign intellectual property laws will not protect our intellectual property rights to the same extent as intellectual property
laws in the U.S. The rights provided by a patent are finite in time. Over the coming years, certain patents relating to current
products will expire in the U.S. and abroad which may allow third parties to exploit those technologies. In the absence of
significant patent protection, we may be vulnerable to competitors who attempt to copy our products, processes or technology.
In addition to the patents we have been issued or we have acquired, we license patents from others on a variety of terms
and conditions.
We are engaged in intellectual property litigation as described in Note 14 to our consolidated financial statements entitled
"Litigation and Related Matters," and as may also be described herein, and we may be notified in the future of claims that we
may be infringing, misappropriating or otherwise violating the intellectual property rights of third parties. In connection with
any such claims, we may seek to enter into settlement and/or licensing arrangements. There is a risk in these situations that no
license will be available or that a license will not be available on reasonable terms. Alternatively, we may decide or be required
to litigate such claims. A successful claim against us may require us to remove the alleged infringing product from the market
or to design around the third party's patent, potentially resulting in less market demand for the product.
Regulatory
The manufacture, sale, lease and service of medical diagnostic and surgical devices intended for commercial use are
subject to extensive governmental regulation by the FDA in the U.S. and by a variety of regulatory agencies in other countries.
Under the Federal Food, Drug and Cosmetic Act, known as the FD&C Act, manufacturers of medical products and devices
must comply with certain regulations governing the design, testing, manufacturing, packaging, servicing and marketing of
medical products. Some of our products are also subject to the Radiation Control for Health and Safety Act, administered by the
FDA, which imposes performance standards and record keeping, reporting, product testing and product labeling requirements
for devices that emit radiation, such as x-rays. FDA product approvals may be withdrawn or suspended if compliance with
regulatory standards is not maintained or if problems occur following initial marketing.
The FDA classifies medical devices into three classes based on risk. Regulatory control increases from Class I (lowest
risk) to Class III (highest risk). The FDA generally must clear or approve the commercial sale of new medical devices in
Classes II and III. Commercial sales of our Class II (except for Class II exempt devices) and Class III medical devices within
the U.S. must be preceded by either a pre-market notification filing pursuant to Section 510(k) of the FD&C Act (Class II) or
the granting of a pre-market approval, or PMA (Class III). Our Class I and Class II exempt medical devices must follow
Hologic’s internal Quality System processes prior to commercialization and throughout their product lifecycle. All classes of
devices must meet FDA's quality system (QS), establishment registration, medical device listing, labeling and medical device
reporting (MDR) regulations. The FDA can authorize the emergency use of an unapproved medical product or an unapproved
use of an approved medical product, referred to as Emergency Use Authorization, or EUA, for certain emergency circumstances
after the Health and Human Services Secretary has made a declaration of emergency justifying authorization of emergency use.
An EUA allows use in an emergency to diagnose, treat, or prevent serious or life-threatening diseases or conditions caused by
emerging infectious disease threats when there are no adequate, approved, and available alternatives. The FDA may also waive
otherwise-applicable current good manufacturing practice (CGMP) requirements to accommodate emergency response needs.
In March 2020, the FDA granted EUA for our Panther Fusion SARS-CoV-2 assay for testing for the COVID-19 virus. In May
2020, the FDA granted EUA for our Aptima SARS-CoV-2 assay for use on our standard Panther instrument.
A 510(k) pre-market notification filing must contain information establishing that the device to be sold is substantially
equivalent to a device commercially distributed prior to May 28, 1976 or to a device that has been determined by the FDA to be
substantially equivalent. The PMA procedure involves a complex and lengthy testing process that is subject to review by the
FDA and may require several years to obtain. We may need to first obtain an investigational device exemption (for significant
risk devices), known as an IDE, in order to conduct extensive clinical testing of the device to obtain the necessary clinical data
for submission to the FDA. The FDA will approve a PMA only if after evaluating the supporting technical data it finds that the
PMA contains sufficient, valid scientific evidence to assure that the device is safe and effective for its intended use(s). This
approval may be granted with post-approval requirements including inspection of manufacturing facilities and/or additional
patient follow-up for an indefinite period of time.
Our Biotheranostics laboratory in San Diego, California and the laboratories that purchase certain of our products,
including the Aptima SARS-CoV-2 EUA, Aptima Flu Multiplex EUA, Fusion SARS-CoV-2 EUA, ThinPrep System, ThinPrep
Imaging System, Rapid Fetal Fibronectin Test, Aptima Combo 2, Aptima HPV tests and Aptima HIV-1 Quant, HCV Quant Dx,
HBV Quant, Aptima Trichomonas Vaginalis (Trich), Aptima Mycoplasma Genitalium (MGen), Aptima HSV 1 & 2, Aptima
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BV, Aptima CV/TV, and Panther Fusion Assays are subject to extensive regulation under the Clinical Laboratory Improvement
Amendments of 1988, or CLIA, which requires laboratories to meet specified standards in the areas of personnel qualifications,
administration, participation in proficiency testing, patient test management, quality control, quality assurance and inspections.
Adverse interpretations of current CLIA regulations or future changes in CLIA regulations could have an adverse effect on
sales of any affected products or services. These laboratories are also licensed by the appropriate state agencies in the states in
which they operate, where such licensure is required. In addition, our laboratories hold state licenses or permits, as applicable,
from various states to the extent that they accept specimens from one or more of these states, each of which requires out-of-state
laboratories to obtain licensure. If a laboratory is out of compliance with CLIA or with state laws or regulations governing
licensed laboratories, penalties may include suspension, limitation or revocation of the license or CLIA certificate, assessment
of financial penalties or fines, or imprisonment. Loss of a laboratory's CLIA certificate or state license may also result in the
inability to receive payments from state and federal health care programs as well as private third party payors.
Certain analyte specific reagents, referred to as ASR products, as with other Class I products, may be sold without 510(k)
clearance or PMA approval. However, ASR products are subject to significant restrictions. The manufacturer may not make
clinical or analytical performance claims for the ASR product, may not promote their use with specific laboratory equipment
and may only sell the ASR product to clinical laboratories that are qualified to run high complexity tests under CLIA. Each
laboratory must validate the ASR product for use in diagnostic procedures as a laboratory developed test.
We are also subject to a variety of federal, state and foreign laws which broadly relate to our interactions with healthcare
practitioners and other participants in the healthcare system, including, among others, the following:
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anti-kickback and anti-bribery laws, such as the Foreign Corrupt Practices Act, or the FCPA, the UK’s Bribery Act
2010, or the UK Anti-Bribery Act;
laws regulating the confidentiality of sensitive personal information and the circumstances under which such
information may be released and/or collected, such as the Health Insurance Portability and Accountability Act of 1996,
or HIPAA, the Health Information Technology for Economic and Clinical Health Act, or HITECH Act, and the
European Union General Data Protection Regulation, or GDPR; and
healthcare reform laws, such as the Patient Protection and Affordable Care Act and the Health Care and Education
Affordability Reconciliation Act of 2010, which we refer to together as PPACA, which include new regulatory
mandates and other measures designed to constrain medical costs, as well as stringent new reporting requirements of
financial relationships between device manufacturers and physicians and teaching hospitals.
In addition, we are subject to numerous federal, state, foreign and local laws relating to safe working conditions,
manufacturing practices, environmental protection, fire hazard control and disposal of hazardous or potentially hazardous
substances, data privacy and protection among others. We may be required to incur significant costs to comply with these laws
and regulations in the future and complying with these laws may result in a material adverse effect upon our business, financial
condition and results of operations.
Sales of medical devices outside of the U.S. are subject to foreign requirements that vary widely from country to country.
For example, our ability to market our products outside of the U.S. is contingent upon maintaining our International Standards
Organization, or ISO, Quality System certification, complying with European directives and in some cases receiving specific
marketing authorization from the appropriate foreign regulatory authorities. Foreign registration is an ongoing process as we
register additional products and/or product modifications.
The time required to obtain approval from a foreign country to market and sell our products may be longer or shorter than
that required for FDA approval and the requirements may differ. In addition, we may be required to meet the FDA’s export
requirements or receive FDA export approval for the export of our products to foreign countries.
Our products are also subject to approval and regulation by foreign regulatory and safety agencies. For example, the EU
has adopted the EU Medical Device Regulation (the "EU MDR") and the In Vitro Diagnostic Regulation (the "EU IVDR"),
each of which impose stricter requirements for the marketing and sale of medical devices, including in the area of clinical
evaluation requirements, quality systems and post-market surveillance. Manufacturers of currently approved medical devices
had until May 2021 to meet the requirements of the EU MDR and had until May 2022 to meet the EU IVDR. Complying with
the requirements of these regulations has required us to, and may continue to require us to, incur significant expenditures.
Failure to meet these requirements could adversely impact our business in the EU and other regions that tie their product
registrations to the EU requirements. The recently rebranded National Medical Products Administration (formerly CFDA), or
the NMPA, has historically been conservative leading to extended review times. However, more recently, the NMPA has been
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more interactive, which we attribute to its response to the long delays in getting lifesaving medical devices into China. If this
continues, this could favorably affect our ability to introduce new products in the Chinese market.
The regulatory environment in China continues to evolve, and officials in the Chinese government exercise broad
discretion in deciding how to interpret and apply regulations. It is possible that the Chinese government's current or future
interpretation and application of existing or new regulations will negatively impact our China operations, result in regulatory
investigations or lead to fines or penalties.
We anticipate that governmental authorities will continue to scrutinize the healthcare industry closely and that changes in
laws, regulations or policies by governmental authorities may cause increases in uncertainties and compliance costs, exposure
to litigation and other adverse effects to our business and operations. Delays in receipt of, or failure to obtain, clearances or
approvals for future products could delay or preclude realization of product revenues from new products or result in substantial
additional costs which could decrease our profitability.
For additional information about the regulations to which our business is subject and the impact such regulations may
have on our business, see the disclosures under the captions “Manufacturing” and “Reimbursement” in this Item 1, and “Risk
Factors” in Item 1A below.
Reimbursement
Market acceptance of our medical products in the U.S. and other countries is dependent upon the purchasing and
procurement practices of our customers and patient need for our products and procedures and, the coverage and reimbursement
of patients’ medical expenses by government healthcare programs, private insurers or other healthcare payors. In the U.S., the
Centers for Medicare & Medicaid Services, known as CMS, establishes coverage policies and payment rates for Medicare
beneficiaries. CMS publishes payment rates for physician, hospital, laboratory and ambulatory surgical center services on an
annual basis. Under current CMS policies and regulations, varying payment levels have been established for tests and
procedures performed using our products. Coverage policies for Medicare patients may vary by regional Medicare contractor in
the absence of a national coverage determination and payment rates for procedures may vary based on the geographic price
index. Coverage policies and reimbursement rates for Medicaid patients are dependent on each state Medicaid plan and will
vary. Coverage policies and reimbursement rates for patients with private insurance is dependent on state and federal
requirements as well as individual private payor’s decisions. Moreover, private insurance carriers may choose not to follow the
CMS coverage policies or payment rates. The use of our products outside of the U.S. is similarly affected by reimbursement
policies adopted by foreign regulatory authorities and insurance carriers.
Healthcare policy and payment reform proposals and medical cost containment measures are being adopted in the U.S.
and in many foreign countries. The ability of our customers to obtain adequate reimbursement for our products and services
from private and governmental third-party payors is critical to the success of medical technology companies because it may
affect which products customers purchase and the prices they are willing to pay. Reimbursement and coverage vary by country
and can significantly impact acceptance of new products and technologies. Even if we develop a promising new product, we
may find limited demand for the product unless reimbursement approval and coverage is obtained from private and
governmental third-party payors. Further, ongoing legislative or administrative reform to the reimbursement system in the U.S.
and other countries may impact reimbursement for procedures using our medical products and/or limit coverage for those
procedures facilitated by our products. This includes price regulation, competitive bidding and tendering, coverage and payment
policies, comparative effectiveness of therapies, technology assessments and managed-care arrangements. These trends could
have a material adverse effect on our business, financial condition or results of operations.
Human Capital
We view human capital management and the strength of our employees as integral to the long-term success of our
business and the strengthening of our communities. We understand that we rely on our employees worldwide to propel our
organization forward with great ideas, innovations and leadership.
As of September 24, 2022, we had 6,944 full-time employees, including 2,101 in manufacturing operations, 1,684 in sales
and marketing, 1,480 in support services, 925 in research and development, and 754 in general administration. Approximately
4,045 of these employees are in the U.S. and approximately 2,899 were outside the U.S. In various countries outside the U.S.,
certain of our employees are unionized and, where local law requires, participate in works councils.
Employee Engagement
Our goal is to develop and maintain a talented, engaged and diverse workforce that has a positive impact on our
performance, and on our customers and their patients. We have been conducting an annual engagement survey since 2015 in
which most of our employees regularly participate. We believe our foundation of employee engagement, our commitment to
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our employees, and their commitment to each other fortifies our leaders and teams and improves their business performance.
We also offer a range of programs to develop our managers and enhance our leadership across the Company. Our professional
development efforts are aimed at increasing organizational talent and capabilities and identifying and developing potential
successors for key leadership positions.
Compensation and Benefits
We invest in the physical, emotional and financial well-being of our employees through our robust compensation and
benefit programs. These programs (which vary by country/region) include a variety of health plan options, tax-favorable
savings accounts and other wellness offerings.
Diversity Drives Performance
We are committed to creating an inclusive and diverse work environment that promotes equal opportunity, dignity and
respect, starting with our Board and our Leadership team. Of our eight directors, three, representing 38% of the Board, are
women and one of our directors self-identifies as Asian. For each of the past 11 years, women have comprised over 30% of our
Board. Also, three of our directors were born outside of the United States, and two were predominantly educated outside of the
United States, which we believe promotes global diversity for our Board. We believe that our focus on the lives of women has
helped us to attract a diverse workforce and build an inclusive ethos where different perspectives are valued and respected.
Building a diverse workforce begins with our hiring practices and extends to our access to opportunities, strategic development
and promotion of internal talent. We seek to identify and develop high-potential women and other diverse individuals within the
Company. In addition to women holding several key roles within the Company (Chief Financial Officer; Chief Human
Resources Officer; Vice President,Global Tax and Treasury; Vice President of Finance, Breast and Skeletal Health; Vice
President of Internal Audit; and Chief of Staff), African American leaders have assumed important leadership roles as Division
President, GYN Surgical, Vice President of Sales, Breast and Skeletal Health and Corporate Secretary. Additionally, given that
our commercial teams are an important pipeline for senior management, we are pleased that a significant number of our
commercial team members below the level of vice president are women and/or people of color.
We strive to hire the most qualified person for the job and believe that, over time, this will lead to an increasingly diverse
workforce. As a part of finding the most qualified people, we are committed to ensuring that diverse slates of candidates are
identified and considered for all roles, from the boardroom and c-suite to all levels of the workforce. We believe our focus on
talent identification, development, engagement and succession planning has been particularly successful in developing a deep
and diverse talent pipeline.
Health and Safety
We seek to comply in letter and in spirit with applicable health and safety laws and regulations and implement programs,
policies and procedures to achieve compliance throughout the Company. We also establish our own environmental health and
safety standards in addition to those that are legally required. We employ management systems and procedures designed to
protect human safety, health, and the environment. We seek to reduce risk and protect our employees and communities by
employing safe technologies and operating procedures, and by maintaining a business continuity program to stay prepared for
emergencies. We have also developed safety rules and procedures to address behaviors and work practices that can lead to
accidents and injuries. Safety performance is assessed throughout the year by management and during annual performance
reviews.
In the beginning of the COVID-19 pandemic, we took precautions to protect the health and safety of our employees by
instituting robust hygiene practices, implementing temperature scanning stations, installing temporary safety structures, and
increasing our cleaning protocols. For our front-line employees who came to our facilities throughout the COVID-19 pandemic
to develop and manufacture our COVID-19 tests, or who installed Panther instruments in locked-down hospitals during the
most uncertain times of the COVID-19 pandemic, we were able to provide extraordinary financial awards.
We continue to actively monitor the COVID-19 pandemic and variants, and respond based on guidance from U.S. and
global health organizations, relevant governmental guidance and evolving practices. In addition, in response to the continuing
challenges stemming from the COVID-19 pandemic, we developed several employee-focused initiatives to support the
physical, mental, and financial well-being of our employees. These initiatives include providing enhanced accident and critical
illness insurance, increasing access to telehealth services, developing an employee assistance program that provides mental
health therapy, wellness coaching, and medication management, and offering subscriptions to self-care mobile apps.
Community Engagement and Volunteerism
We take the role we play as leaders in the communities where we live and work seriously. Our philanthropic and
charitable efforts are an important part of our culture. We center our giving efforts in three specific areas to maximize our
impact in ways that align with the values of our employees and customers: (i) women's health, and other healthcare fields in
which Hologic operates; (ii) science, technology, engineering, and math education (STEM), especially for underprivileged
groups; and (iii) social and racial equality, especially in healthcare. In fiscal 2022, we announced an expansion of our
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philanthropic activities, pledging to donate $5 million from our charitable fund over the year to further support the communities
where our employees live and work.
We also support employees in giving back to community organizations through volunteering and matching donations. To
that end, we further expanded our support for local non-profit groups, by providing our U.S. colleagues an additional paid day
off to engage in community service. We also have continued to strengthen our scholarship funds. The Hologic Scholarship
Fund awards scholarships of $2,500 to $5,000 for employees' children and grandchildren. We also support minority students
near our largest U.S. facilities by providing scholarship funding to three non-profit organizations that help students from
underserved communities become the first in their family to attend college.
Seasonality
Worldwide sales, including U.S. sales, do not reflect any significant degree of seasonality; however, customer purchases
of our GYN Surgical products have been historically lower in our second fiscal quarter compared to our other fiscal quarters.
Our respiratory infectious disease product line (including our assays for the detection of SARS-CoV-2) within our Diagnostics
segment is also subject to significant seasonal and year-over-year fluctuations. In addition, the summer months, which occur
during our fourth fiscal quarter, typically have had lower order rates internationally for most of our products.
Item 1A. Risk Factors
In evaluating our business, the risks described below, as well as other information contained in this Annual Report and in
our other filings with the SEC should be considered carefully. Additional risks not presently known to us or that we currently
deem immaterial may also adversely affect our business. The occurrence of any of these events or circumstances could
individually or in the aggregate have a material adverse effect on our business, financial condition, cash flow or results of
operations. This report contains forward-looking statements; please refer to the cautionary statements made under the heading
"Special Note Regarding Forward-Looking Statements" for more information on the qualifications and limitations on forward-
looking statements.
GLOBAL CHALLENGES, INCLUDING MACROECONOMIC CONDITIONS AND RELATED FINANCIAL RISKS
The continuing worldwide macroeconomic and geopolitical uncertainty may adversely affect our business and prospects,
both domestically and internationally.
Continued concerns about the systemic impact of potential long-term and wide-spread recession and geopolitical issues,
including the war in Ukraine, have contributed to increased market volatility and diminished expectations for economic growth
in the world. Our business and results of operations have been and may continue to be adversely impacted by changes in
macroeconomic conditions, including inflation, rising interest rates and availability of capital markets. Uncertainty about global
economic conditions, particularly in emerging markets and countries with government-sponsored healthcare systems, may also
cause decreased demand for our products and services and increased competition, which could result in lower sales volume and
downward pressure on the prices for our products, longer sales cycles, and slower adoption of new technologies. A weakening
of macroeconomic conditions may also adversely affect our suppliers, which could result in interruptions in supply.
Market acceptance of our medical products in the U.S. and other countries is dependent upon the medical equipment
purchasing and procurement practices of our customers, patient need for our products and procedures and the reimbursement of
patients' medical expenses by government healthcare programs and third-party payors. The continuing uncertainty surrounding
global economic conditions and financial markets may cause the purchasers of medical equipment to decrease their medical
health insurance premiums and procurement activities. Economic uncertainty, an increase in unemployment rates, as well as
increasing health insurance premiums, co-payments and deductibles may continue to result in cost-conscious consumers
making fewer trips to their physicians and specialists, which in turn would adversely affect demand for our products and
procedures. Furthermore, governments and other third-party payors around the world facing tightening budgets could move to
further reduce the reimbursement rates or the scope of coverage offered, which could adversely affect sales of our products.
Our international sales are often denominated in foreign currencies, including the Euro, UK Pound and Renminbi.
Changes in currency exchange rates, particularly the increase in the value of the dollar against any such foreign currencies, may
reduce the reported value of our revenues outside the U.S. and associated cash flows and our ability to compete effectively in
foreign markets. In addition, such fluctuations can also result in foreign currency exchange losses. We cannot predict changes
in currency exchange rates, the impact of exchange rate changes, nor the degree to which we will be able to manage the impact
of currency exchange rate changes. We currently have limited hedging arrangements in place to mitigate some of the impact of
negative exchange rates.
Our international operations and foreign acquisitions expose us to additional operational challenges that we might not
otherwise face.
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International expansion is a key component of our growth strategy. In fiscal 2022, 28.7% of our revenue came from
outside of the U.S. As we grow internationally, our future and existing international operations may subject us to a number of
additional risks and expenses, any of which could harm our operating results. These risks and expenses include:
political and economic changes and disruptions, export/import controls and tariff regulations;
difficulties in developing staffing and simultaneously managing operations in multiple locations as a result of, among
other things, distance, language and cultural differences;
governmental currency controls;
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requirements);
protectionist laws and business practices that favor local companies;
difficulties in the collection of trade accounts receivable;
difficulties and expenses related to implementing internal controls over financial reporting and disclosure controls and
procedures;
expenses associated with customizing products for clients in foreign countries;
possible adverse tax consequences;
the inability to obtain and maintain required regulatory approvals or favorable third-party reimbursement;
operation in parts of the world where strict compliance with anti-bribery laws may conflict with local customs and
practices;
the inability to effectively obtain, maintain, protect or enforce intellectual property rights, reduced protection for
intellectual property rights in some countries, and the inability to otherwise protect against clone or “knock off”
products;
the lack of ability to enforce non-compete agreements with former owners of acquired businesses competing with us in
China and other foreign countries; and
lower margins on a number of our products sold outside of the U.S.
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In addition, government policies on international trade and investment such as import quotas, capital controls or tariffs,
whether adopted by individual governments or addressed by regional trade blocks, can affect the demand for our products and
services, impact the competitive position of our products or prevent us from being able to sell products in certain countries. The
implementation of more restrictive trade policies, such as more detailed inspections, higher tariffs or new barriers to entry,
could negatively impact our business, results of operations and financial condition. For example, a government's adoption of
"buy national" policies or retaliation by another government against such policies could have a negative impact on our results of
operations.
Additionally, the regulatory environment in China continues to evolve, and officials in the Chinese government exercise
broad discretion in deciding how to interpret and apply regulations. It is possible that the Chinese government's current or future
interpretation and application of existing or new regulations will negatively impact our China operations, result in regulatory
investigations or lead to fines or penalties.
BUSINESS CONTINUITY AND RELIANCE ON THIRD PARTIES
Supply Chain and Manufacturing
Supply chain disruptions and constraints and inflationary pressures have had, and may continue to have, a material adverse
effect on our ability to procure raw materials and components, including semiconductor chips, and are adversely affecting
our ability to meet customer demand for, and increasing our costs to manufacture, warehouse, and transport, certain of our
products.
Global supply constraints and cost impacts as a result of worldwide economic disruptions, electronic component
shortages, fear of future or ongoing pandemics, inflation, recessionary conditions and geopolitical events, including the war in
Ukraine, are impacting our ability to procure critical raw materials and components, including semiconductor chips, and are
adversely affecting our ability to meet customer demand for, and increasing our costs to manufacture, transport and warehouse
a certain subset of our products. Obtaining alternative sources of raw materials and components could involve significant costs
and regulatory challenges and may not be available to us on reasonable terms, if at all. In particular, our ability to manufacture
our Breast Health capital equipment products, primarily, but not limited to, our 3D Dimensions systems, Trident specimen
radiography systems, Affirm Prone Biopsy systems and Brevera systems, is dependent on the supply of such raw materials and
components, including semiconductor chips. If we remain unable to obtain sufficient quantities of raw materials and
components on commercially reasonable terms or in a timely manner, our ability to manufacture our capital equipment
products, in particular, our Breast Health products, on a timely and cost-competitive basis could materially adversely affect our
revenues and results of operations and harm our competitive position and reputation.
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Our reliance on one third-party manufacturer for certain of our product lines and a limited number of suppliers for some
key raw materials, components and subassemblies for our products exposes us to increased risks associated with production
delays, delivery schedules, manufacturing capability, quality control, quality assurance and costs.
We have sole source third-party manufacturers for each of our Panther and Tigris molecular diagnostics instruments and
for our Skeletal Health products. Similarly, we rely on one or a limited number of suppliers for some key components or
subassemblies for our products due to cost, quality, expertise or other considerations. We have no firm long-term volume
commitments with certain of our sole source suppliers, including the manufacturers of our Panther or Tigris instruments.
Similarly, we rely on one or a limited number of suppliers for some key raw materials for our products due to cost, quality,
expertise or other considerations, and some of these suppliers are competitors. For example, F. Hoffmann-LaRoche Ltd, a direct
competitor of our Diagnostics business, is the parent company of Roche, our current supplier of certain key raw materials for
certain of our amplified NAT diagnostic assays. GE Healthcare Bio-Sciences Corp., an affiliate of GE, supplies us with the
membranes used in connection with our ThinPrep product line. GE is a direct competitor with our Breast Health and Skeletal
Health businesses. Moreover, we use certain components in our products, including semiconductor chips, that have been the
subject of global supply chain shortages and disruptions. If any of our sole source manufacturers or suppliers, or other third-
party manufacturers or suppliers, experiences delays, disruptions, capacity constraints or quality control problems in its
development or manufacturing operations or becomes insolvent or otherwise fails to supply us with goods in sufficient
quantities, including as a result of disruptions caused by the continued impact of COVID-19, other epidemics or pandemics,
natural disasters, supplier facility shutdowns, or otherwise, then shipments to our customers could be delayed, which would
decrease our revenues and harm our competitive position and reputation. Moreover, the failure of a supplier to provide
sufficient quantities, acceptable quality and timely delivery of goods at an acceptable price, or an interruption in the delivery of
goods from such a supplier could adversely affect our business and results of operations. Obtaining alternative sources of
supply of products, components, subassemblies or raw materials could involve significant delays and other costs and regulatory
challenges and may not be available to us on reasonable terms, if at all.
We may in the future need to find new contract manufacturers or suppliers to replace existing manufacturers or suppliers,
increase our volumes or reduce our costs. We may not be able to find contract manufacturers or suppliers that meet our needs,
including regulatory requirements, and even if we do, the process of qualifying such alternative manufacturers and suppliers is
often expensive and time consuming. As a result, we may lose revenues and our customer relationships may suffer.
Business Continuity
Interruptions, delays, shutdowns or damage at our manufacturing or laboratory facilities could harm our business.
In most cases, the manufacturing and warehousing of each of our products is concentrated in one or a few locations. In
addition, we rely on a single laboratory facility to process each of our Biotheranostics gene expression tests for breast cancer.
An interruption in manufacturing, testing capabilities or warehousing at any of these facilities, as a result of equipment failure,
transportation interruptions, disruptions caused by the continued impact of COVID-19, other epidemics or pandemics, natural
disaster, environmental factors or property damage could reduce, delay or prevent the production and distribution of our
products. Our facilities and those of our contract manufacturers or suppliers are also subject to the risk of catastrophic loss due
to unanticipated events, such as fires, earthquakes, explosions, floods or weather conditions. Our facilities may experience plant
shutdowns, strikes or other labor disruptions, or periods of reduced production as a result of equipment failures, loss of power,
gray outs, delays in deliveries or extensive damage, which could harm our business and prospects. Some of our manufacturing
operations are located outside the U.S., including in Costa Rica and the United Kingdom. Those manufacturing operations are
also subject to additional challenges and risks associated with international operations described herein.
COMPETITION AND BUSINESS DEVELOPMENT
We face intense competition from other companies and may not be able to compete successfully.
The markets in which we sell our products are intensely competitive, subject to rapid technological change and may be
significantly affected by new product introductions and other market activities of industry participants, and these competitive
pressures may reduce the demand and prices for our products. Other companies may develop products that are superior to and/
or less expensive than our products. Improvements in existing competitive products or the introduction of new competitive
products may reduce our ability to compete for sales, particularly if those competitive products demonstrate better safety or
effectiveness, clinical results, ease of use or lower costs. Organizational changes we have made or may make to streamline and
improve customer experience may not have the intended effect and may instead harm our competitive position and reputation.
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We also developed assays to detect COVID-19. While we have seen significant demand for our COVID-19 assays, other
companies are working to produce or have produced tests for COVID-19 (including so-called high throughput nucleic acid
tests, rapid antigen tests and at-home testing solutions) which may lead to the diversion of customers away from us and toward
other companies. Moreover, considerable uncertainty remains as to the demand for ongoing COVID-19 testing, and thus, for
our COVID-19 assays. There is no guarantee that current or anticipated demand will continue, or if demand does continue or
increases, that we will be able to produce in quantities to meet the demand. As COVID-19 testing declines, customers may also
consolidate their molecular testing menu to high throughput, high automation platforms which may further increase the
competition our Panther and Panther Fusion instruments face. A significant decline in demand for our COVID-19 assays or a
reduction in the reimbursement rates for our COVID-19 assays without a corresponding increase in our other businesses could
have a material, adverse effect on our results of operations, cash flow and financial position.
In addition, some companies may have significant competitive advantages over us, which may make them more attractive
to hospitals, clinics, radiology clients, group purchasing organizations, laboratories, and physicians, including:
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greater brand recognition;
larger or more established distribution networks and customer bases;
a broader product portfolio, resulting in the ability to offer rebates or bundle products to offer discounts or incentives
to gain a competitive advantage;
higher levels of automation and greater installed bases of such equipment;
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• more extensive research, development, sales, marketing, and manufacturing capabilities and greater financial
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resources; and
greater technical resources positioning them to continue to improve their technology in order to compete in an
evolving industry.
Challenges in the development of our products could materially impact our long-term success.
Our growth depends in large part on our ability to identify and develop new products or new indications for or
enhancements of existing products. The development of new products and enhancement of existing products requires
significant investment in research and development, clinical trials and regulatory approvals. The results of our product
development efforts may be affected by a number of factors, including our ability to anticipate customer needs, innovate and
develop new products, complete clinical trials, obtain regulatory clearances and approvals and reimbursement in the U.S. and
abroad, manufacture products in a cost-effective manner, obtain, maintain, protect and enforce appropriate intellectual property
protection for our products, gain and maintain market approval of our products and access capital. If we are not able to
successfully enhance existing products or develop new products, our products may be rendered obsolete or uncompetitive by
changing technology or new industry standards. We cannot assure that any products now in development or that we may seek to
develop in the future will achieve technological feasibility, obtain regulatory approval or gain market acceptance, and we may
be unable to recover all or a meaningful part of our investment in such products and technologies.
The markets for our newly developed products and newly introduced enhancements to our existing products may not develop
as expected.
The successful commercialization of our newly developed products and newly introduced enhancements to our existing
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products are subject to numerous risks, both known and unknown, including:
uncertainty of the development of a market for such product;
trends relating to, or the introduction or existence of, competing products or technologies that may be more effective,
safer or easier to use than our products or technologies;
the perception of our products as compared to other products;
recommendation and support for the use of our products by influential customers, such as highly regarded hospitals,
physicians and treatment centers;
the availability and extent of data demonstrating the clinical efficacy of our products or treatments;
competition, including the presence of competing products sold by companies with longer operating histories, more
recognizable names and more established distribution networks; and
other technological developments.
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Often, the development of a significant market for a product will depend upon the establishment of a reimbursement code
or an advantageous reimbursement level for use of the product. Moreover, even if addressed, such reimbursement codes or
levels frequently are not established until after a product is developed and commercially introduced, which can delay the
successful commercialization of a product. If we are unable to successfully commercialize and create a significant market for
our newly developed products and newly introduced enhancements to our existing products our business and prospects could be
harmed.
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If we cannot maintain our current corporate collaborations and enter into new corporate collaborations, our product
development could be delayed and our revenue could be adversely impacted.
We have relied and/or expect to rely on corporate collaborators for funding development, marketing, distribution, and the
commercialization of certain products. If any of our corporate collaborators were to breach, terminate, fail to renew our
agreements or otherwise fail to properly conduct its obligations in a timely manner, the development or commercialization and
subsequent marketing of the products contemplated by the collaboration could be delayed or terminated. Further, we would be
required to devote additional resources to product development or marketing, to terminate some development programs or to
seek alternative corporate collaborations with certain partners or companies that could make it more difficult for us to enter into
advantageous business transactions or relationships with others. Any of the foregoing risks could harm our business and
prospects.
Our long-term success will depend upon our ability to execute on business development activities and integrate acquired
businesses.
As part of our long-term strategy, we are engaged in business development activities including evaluating future
acquisitions, joint development opportunities, technology licensing arrangements and other opportunities to further expand our
presence in or diversify into priority growth areas by accessing new products and technologies. We may not be able to identify
appropriate business development activities or acquisition candidates, consummate transactions or obtain agreements with
favorable terms, if at all. We may also be subject to increasing regulatory scrutiny from competition and antitrust authorities in
connection with acquisitions. If we are successful in pursuing future acquisitions, we may face significant competition, be
required to expend significant funds, incur additional debt or other obligations, or issue additional securities, which may
negatively affect our operating results and financial condition. If we spend significant funds or incur additional debt or
obligations, our ability to obtain financing for working capital or other purposes could be adversely affected, and we may be
more vulnerable to economic downturns and competitive pressures. During fiscal 2021, we made a number of tactical
acquisitions which complemented our existing businesses. We continue to integrate those acquisitions. Any inability to
successfully integrate new businesses, including our recent acquisitions, decreases in customer loyalty or product orders, failure
to retain or develop the acquired workforce, failure to realize anticipated economic, operational and other benefits and synergies
in a timely manner, failure to establish and maintain appropriate controls or unknown or contingent liabilities could adversely
affect our ability to realize the anticipated benefits of any new product or acquisition. The integration of an acquired business,
whether or not successful, requires significant efforts which may result in additional expenses and divert the attention of our
management and technical personnel from other projects. Acquisitions, in particular, are inherently risky, and we cannot
guarantee that any past or future transaction will be successful.
GLOBAL PUBLIC HEALTH CONCERNS
Public health crises, such as the COVID-19 pandemic, have had, and could in the future have, a negative effect on our
business.
Pandemics or disease outbreaks, such as the COVID-19 pandemic, have created and may continue to create significant
volatility, uncertainty and economic disruption in the markets we sell our products into and operate in, primarily the U.S.,
Europe, and Asia-Pacific and may negatively impact business and healthcare activity globally. In response to the COVID-19
pandemic, governments around the world have imposed measures designed to reduce the transmission of COVID-19 and
individuals continue to respond to the fear of contracting COVID-19. In particular, elective procedures and exams were delayed
or cancelled, there has been a significant reduction in physician office visits, and hospitals postponed or canceled capital
purchases as well as limited or eliminated services. While elective procedures and exams and capital purchases have increased
from initially depressed levels, the reduction in elective procedures, exams and capital purchases has had, and we believe may
continue to have, a negative impact on the sales of most of our products (other than our COVID-19 assays and related systems
and ancillaries). Additionally, governments and other third-party payors around the world facing tightening budgets could move
to further reduce the reimbursement rates or the scope of coverage offered, which could further adversely affect sales of our
products.
The extent to which fear of exposure to or actual effects of COVID-19, new variants, disease outbreak, epidemic or a
similar widespread health concern impacts our business will depend on future developments, which are highly uncertain and
cannot be predicted with confidence, such as the speed and extent of geographic spread of the disease, the duration of the
outbreak, travel restrictions, the efficacy of vaccination and treatment; impact on the U.S. and international healthcare systems,
the U.S. economy and worldwide economy; the timing, scope and effectiveness of U.S. and international governmental
response; and the impact on the health, well-being and productivity of our employees.
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CUSTOMER CONCENTRATION AND DISTRIBUTORS
Our Diagnostics segment depends on a small number of customers for a significant portion of its product sales, and the loss
of any of these customers or any cancellation or delay of a large purchase by any of these customers could significantly
reduce revenues in our Diagnostics segment.
Although we do not currently have any customers that represent more than 10% of our consolidated revenues, or more
than 10% of a business segment's revenue in fiscal 2022 and 2021, historically a material portion of product sales in our
Diagnostics segment came from (and we anticipate will continue to come from) a limited number of customers. The loss of any
of these key customers, or a significant reduction in sales volume or pricing to these customers, could significantly reduce our
Diagnostics segment revenues or profitability.
We utilize distributors for a portion of our sales, the loss of which could harm our revenues in the territory serviced by these
distributors.
We rely on strategic relationships with a number of key distributors for sales and service of our products. If any of our
strategic relationships terminate without replacement or if our strategic partners fail to perform their contractual obligations, our
revenues and/or ability to service our products in the territories serviced by these distributors could be adversely affected. We
do not control our distributors, and these parties may not be successful in marketing our products. These parties may fail to
commit the necessary resources to market and sell our products to the level of our expectations.
If we elect to distribute new products directly, we will have to invest in additional sales and marketing resources,
including additional field sales personnel, which would significantly increase future selling, general and administrative
expenses. If we fail to successfully market our products, our product sales will decrease. We may also be exposed to risks as a
result of transitioning a territory from a distributor sales model to a direct sales model, such as difficulties maintaining
relationships with specific customers, hiring appropriately trained personnel or ensuring compliance with local product
registration requirements, any of which could result in lower revenues than previously received from the distributor in that
territory.
TALENT AND EMPLOYEE RETENTION
Our success depends on our ability to attract, motivate and retain key personnel and plan for future executive transitions.
The loss of any of our key personnel, particularly executive management or key research and development personnel,
could harm our business and prospects and could impede the achievement of our research and development, operational or
strategic objectives. We also continue to face the challenges of maintaining employee well-being, recognizing that the
continued additional financial, family and health burdens that many employees may be experiencing due to the ongoing impacts
of COVID-19, macroeconomic uncertainties, including inflation, and other factors, may adversely impact job performance and
employee retention. Additionally, in our industry, there is substantial competition for key personnel in the regions in which we
operate. We face intense competition for employees, particularly as employees are increasingly able to work remotely. Also,
facilitating seamless leadership transitions for key positions is a critical factor in sustaining the success of our organization. If
our succession planning efforts are not effective, it could adversely impact our business. We continue to assess the key
personnel that we believe are essential to our long-term success. Future organizational changes could also cause our employee
attrition rate to increase. If we fail to effectively manage any organizational and/or strategic changes, our financial condition,
results of operations, and reputation, as well as our ability to successfully attract, motivate and retain key employees, could be
harmed.
CYBERSECURITY AND DATA PRIVACY
Increased cybersecurity requirements, vulnerabilities, threats and more sophisticated and targeted computer crime could
pose a risk to our systems, networks, products, solutions, services and data.
Increased global cybersecurity vulnerabilities, threats, computer viruses, ransomware and phishing attacks and more
sophisticated and targeted cyber-related attacks, as well as cybersecurity failures resulting from human error and technological
errors, pose a risk to the security of Hologic and its customers, business partners' and suppliers' products, systems and networks
and the confidentiality, availability and integrity of data on these products, systems and networks. As the perpetrators of such
attacks become more capable, as cybercrime becomes commoditized, and as critical infrastructure is increasingly becoming
digitized, the risks in this area continue to grow. While we attempt to mitigate these risks by employing a number of measures,
including employee training, monitoring and testing, and maintenance of protective systems and contingency plans, we remain
potentially vulnerable to additional known or unknown threats, and we cannot assure that the impact from such threats will not
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be material. In addition to existing risks, flexible work arrangements, the adoption of new technologies and acquisitions of new
businesses may also increase our exposure to cybersecurity breaches and failures. We also have access to sensitive, confidential
or personal data or information that is subject to privacy and security laws, regulations or customer-imposed controls. Despite
our implementation of controls to protect our systems and sensitive, confidential or personal data or information, we may be
vulnerable to material security breaches, theft, misplaced, lost or corrupted data, employee errors and/or malfeasance (including
misappropriation by departing employees) that could potentially lead to the compromising of sensitive, confidential or personal
data or information, improper use of our systems, software solutions or networks, unauthorized access, use, disclosure,
modification or destruction of information, defective products, production downtimes and operational disruptions. In addition, a
cyber-related attack could result in other negative consequences, including damage to our reputation or competitiveness,
remediation or increased protection costs, litigation or regulatory action. Although we have experienced occasional actual or
attempted breaches of our computer systems, to date we do not believe any of these breaches has had a material effect on our
business, operations or reputation.
Failure to comply with laws relating to the confidentiality of sensitive personal information or standards related to the
transmission of electronic health data, may require us to make significant changes to our products, or incur penalties or
other liabilities.
State, federal and foreign laws, such as the federal Health Insurance Portability and Accountability Act of 1996, or
HIPAA, regulate the confidentiality of sensitive personal information and the circumstances under which such information may
be released. These measures may govern the disclosure and use of personal and patient medical record information and may
require users of such information to implement specified security measures, and to notify individuals in the event of privacy and
security breaches. Evolving laws and regulations in this area could restrict the ability of our customers to obtain, use or
disseminate patient information, or could require us to incur significant additional costs to re-design our products in a timely
manner, either of which could have an adverse impact on our results of operations. Other health information standards, such as
regulations under HIPAA, establish standards regarding electronic health data transmissions and transaction code set rules for
specified electronic transactions, for example transactions involving submission of claims to third-party payors. These standards
also continue to evolve and are often unclear and difficult to apply. Outside the U.S., we are impacted by privacy and data
security requirements at the international, national and regional level, and on an industry specific basis. More privacy and
security laws and regulations are being adopted, and more are being enforced, with potential for significant financial penalties.
In the EU, increasingly stringent data protection and privacy rules have been enacted. The EU General Data Protection
Regulation (GDPR) applies uniformly across the EU and includes, among other things, a requirement for prompt notice of data
breaches to data subjects and supervisory authorities in certain circumstances. The GDPR also requires companies processing
personal data of individuals residing in the EU to comply with EU privacy and data protection rules. Failure to maintain the
confidentiality of sensitive personal information in accordance with the applicable regulatory requirements, or to abide by
electronic health data transmission standards, could expose us to breach of contract claims, fines and penalties, costs for
remediation and harm to our reputation.
THIRD-PARTY REIMBURSEMENT AND GUIDELINES
Healthcare cost containment legislation and the failure of third-party payors to provide appropriate levels of coverage and
reimbursement for the use of products and treatments facilitated by our products could harm our business and prospects.
Sales and market acceptance of our diagnostics, breast and skeletal health and surgical products and the treatments
facilitated by these products are dependent upon the coverage decisions and reimbursement policies established by government
healthcare programs and private health insurers. These policies affect which products customers purchase and the prices they
are willing to pay. Reimbursement varies by country and can significantly impact the acceptance of new products and
technologies. Even if we develop a promising new product, we may find limited demand for the product unless appropriate
reimbursement approval is obtained from private and governmental third-party payors. Further legislative or administrative
reforms to the reimbursement systems in the U.S. and other countries in a manner that significantly reduces reimbursement for
procedures using our diagnostics, breast and skeletal health and surgical products or denies coverage for those procedures
facilitated by our products, including price regulation, competitive bidding and tendering, coverage and payment policies,
comparative effectiveness of therapies, technology assessments and managed-care arrangements, could have a material adverse
effect on our business, financial condition or results of operations.
Guidelines, recommendations and studies published by various organizations may reduce the use of our products.
Professional societies, government agencies, practice management groups, private health/science foundations, and
organizations involved in healthcare issues may publish guidelines, recommendations or studies to the healthcare and patient
communities. Organizations like these have in the past made recommendations about our products and those of our competitors.
If followed by healthcare providers and insurers, such publications could result in decreased use of our products. For example,
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in November 2012, the American Congress of Obstetrics and Gynecologists, known as the ACOG, released updates in which it
recommended less frequent cervical cancer screening similar to guidelines released in March 2012 by the U.S. Preventative
Services Task Force, or the USPSTF, and the American Cancer Society. We believe that these recommendations and guidelines
may have contributed to increased screening intervals for cervical cancer, which we believe has and may continue to adversely
affect our ThinPrep revenues. Our ThinPrep revenues may also be adversely affected by the July 2020 American Cancer
Society cervical cancer screening recommendation for a primary human papillomavirus (HPV) test rather than a Pap test. In
addition, on October 20, 2015, the American Cancer Society issued guidelines recommending that women start annual
mammograms at age 45 instead of 40 and have a mammogram every two years instead of annually. We believe that this
recommendation could result in a decrease in use and purchases of our mammography systems.
REGULATORY AND LEGAL
We operate in a highly regulated industry, and changes in healthcare laws and regulations or our inability to obtain in a
timely manner or at all U.S. or foreign regulatory clearances or approvals for our current and newly developed products and
services or product or service enhancements, could adversely affect our business and prospects.
We operate in a highly regulated industry. As a result, governmental actions may adversely affect our business, operations
or financial condition, including:
•
•
•
•
new laws, regulations or judicial decisions, or new interpretations of existing laws, regulations or decisions, related to
healthcare availability, method of delivery and payment for healthcare products and services;
changes in the FDA and foreign regulatory approval processes that may delay or prevent the approval of new products
and result in lost market opportunity;
changes in FDA and foreign regulations that may require additional safety monitoring, labeling changes, restrictions
on product distribution or use, or other measures after the introduction of our products to market, which could increase
our costs of doing business, adversely affect the future permitted uses of approved products, or otherwise adversely
affect the market for our products; and
new laws, regulations and judicial decisions affecting pricing or marketing practices.
Given the high level of regulatory oversight to which our products are subject, the process of obtaining clearances and
approvals can be costly and time consuming. In addition, there is a risk that any approvals or clearances, once obtained, may be
withdrawn. Most medical devices cannot be marketed in the U.S. without 510(k) clearance or pre-market approval by the FDA.
Any modifications to a device that has received a pre-market approval that affect the safety or effectiveness of the device
require a pre-market approval supplement or possibly a separate pre-market approval, either of which is likely to be time
consuming, expensive and uncertain to obtain. If the FDA requires us to seek one or more pre-market approval supplements or
new pre-market approvals for any modification to a previously approved device, we may be required to cease marketing or to
recall the modified device until we obtain approval, and we may be subject to significant criminal and/or civil sanctions,
including, but not limited to, regulatory fines or penalties. States may also regulate the manufacture, sale and use of medical
devices, particularly those that employ x-ray technology.
Our products are also subject to approval and regulation by foreign regulatory and safety agencies. For example, the EU
has adopted the EU Medical Device Regulation (the “EU MDR”) and the In Vitro Diagnostic Regulation (the “EU IVDR”),
each of which impose stricter requirements for the marketing and sale of medical devices, including in the area of clinical
evaluation requirements, quality systems and post-market surveillance. Implementation of the compliance requirements of these
regulations requires us to incur significant expenditures and utilize resources. Failure to continue to meet these requirements
could adversely impact our business in the EU and other regions that tie their product registrations to the EU requirements.
We anticipate that governmental authorities will continue to scrutinize the healthcare industry closely and that changes in
laws, regulations or policies by governmental authorities may cause increased uncertainties and compliance costs, exposure to
litigation and other adverse effects to our business and operations. Delays in receipt of, or failure to obtain or maintain,
clearances or approvals for future products could delay or preclude realization of product revenues from new or existing
products or result in substantial additional costs which could decrease our profitability.
In addition, maintaining compliance with multiple regulators, and multiple centers within the FDA, adds complexity and
cost to our manufacturing processes. Our manufacturing facilities and those of our contract manufacturers are subject to
periodic regulatory inspections by the FDA and other regulatory agencies, and these facilities are subject to the FDA's Quality
System Regulation and Good Manufacturing Practices. We or our contractors may fail to satisfy these regulatory requirements
in the future, and any failure to do so may prevent us from selling our products.
Some of our activities may subject us to risks under federal and state laws prohibiting “kickbacks” and false or fraudulent
claims.
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We are subject to the provisions of a federal law commonly known as the anti-kickback statute, and several similar state
laws, which prohibit payments intended to induce physicians or others either to refer patients or to acquire or arrange for or
recommend the acquisition of healthcare products or services. While the federal law applies only to products or services for
which payment may be made by a federal healthcare program, state laws often apply regardless of whether federal funds may
be involved. These laws constrain the sales, marketing and other promotional activities of manufacturers of medical devices by
limiting the kinds of financial arrangements, including sales programs that may be used with hospitals, physicians, laboratories
and other potential purchasers of medical devices. Other federal and state laws generally prohibit individuals or entities from
knowingly presenting, or causing to be presented, claims for payment from Medicare, Medicaid, or other third-party payors that
are false or fraudulent, or are for items or services that were not provided as claimed. Similarly, the Patient Protection and
Affordable Care Act also includes stringent reporting requirements of financial relationships between device manufacturers and
physicians and teaching hospitals. Specifically, under one provision of the law, which is commonly referred to as the Physician
Payment Sunshine Act, we are required to collect data on and annually report to CMS certain payments or other transfers of
value to physicians and teaching hospitals and annually report certain ownership and investment interests held by physicians or
their immediate family members. Anti-kickback and false claims laws and the Physician Payment Sunshine Act prescribe civil
and criminal penalties (including fines) for noncompliance that can be substantial.
Similarly, our international operations are subject to the provisions of the U.S. Foreign Corrupt Practices Act of 1977, as
amended ("FCPA"), which prohibits U.S. companies and their representatives from offering or making improper payments to
foreign officials for the purpose of obtaining or retaining business. In many countries, the healthcare professionals we regularly
interact with may meet the definition of a foreign official for purposes of the FCPA. Our international operations are also
subject to various other international anti-bribery laws such as the UK Anti-Bribery Act. Despite meaningful measures that we
undertake to facilitate lawful conduct, which include training and compliance programs and internal policies and procedures,
we may not always prevent unauthorized, reckless or criminal acts by our employees or agents, or employees or agents of
businesses or operations we may acquire. Violations of these laws, or allegations of such violations, could disrupt our
operations, involve significant management distraction and have a material adverse effect on our business, financial condition
and results of operations. We also could be subject to adverse publicity, severe penalties, including criminal and civil penalties,
disgorgement, further changes or enhancements to our procedures, policies and controls, personnel changes and other remedial
actions. Moreover, our failure to comply with domestic or foreign laws could result in various adverse consequences, including
possible delay in approval or refusal to approve a product, recalls, seizures, and withdrawal of an approved product from the
market.
We are subject to the risk of product liability claims relating to our products for which we may not have adequate insurance.
Our business involves the risk of product liability and other claims inherent to the medical device business. If even one of
our products is found to have caused or contributed to injuries or deaths, we could be held liable for substantial damages. We
maintain product liability insurance subject to deductibles and exclusions. There is a risk that the insurance coverage will not be
sufficient to protect us from product and other liability claims, or that product liability insurance will not be available to us at a
reasonable cost, if at all. An under-insured or uninsured claim could harm our business and prospects. In addition, claims could
adversely affect the reputation of the related product, which could damage that product’s competitive position in the market.
The sale and use of our diagnostic products could also lead to product liability claims if someone were to allege that one
of our products contained a design or manufacturing defect that resulted in inaccurate test results or the failure to detect a
disorder for which it was being used to screen, or caused injuries to a patient. Any product liability claim brought against us,
with or without merit, could result in an increase in our product liability insurance rates or the inability to secure additional
coverage in the future. Also, even a meritless or unsuccessful product liability claim could be time consuming and expensive to
defend. This could result in a diversion of management’s attention from our business and adversely affect the perceived safety
and efficacy of our products, which could harm our business and prospects.
We are subject to environmental, health and safety laws and regulations, including related to our use and recycling of
hazardous materials and the composition of our products.
Our research and development and manufacturing processes involve the controlled use of hazardous materials, such as
toxic and carcinogenic chemicals and various radioactive compounds, and the risk of contamination or injury from these
materials cannot be eliminated. In such event, we could be held liable for any resulting damages, and any such liability could be
extensive. From time to time new regulations are enacted, and it is difficult to anticipate how such regulations will be
implemented and enforced. We continue to evaluate the necessary steps for compliance with regulations as they are enacted.
These regulations include, for example, regulations enacted in the EU such as the Registration, Evaluation, Authorization and
Restriction of Chemical Substances, or REACH, which requires the registration of and regulates use of certain chemicals, the
Restriction on the Use of Certain Hazardous Substances in Electrical and Electronic Equipment Directive, or RoHS, which
regulates the use of certain hazardous substances in certain products we manufacture, and the Waste Electrical and Electronic
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Equipment Directive, or WEEE, which requires the collection, reuse and recycling of waste from certain products we
manufacture. These and similar legislation that has been or is in the process of being enacted in Japan, China and various states
of the U.S. may require us to re-design our products to ensure compliance with the applicable standards, for example by
requiring the use of different types of materials. These redesigns or the use of alternative materials may detrimentally impact
the performance of our products, add greater testing lead times for product introductions, result in additional costs or have other
similar effects. In addition, changes in environmental laws and regulations, in particular relating to climate change and
greenhouse gas (“GHG”) emissions, could require us, or our contract manufacturers or suppliers, to install additional
equipment, or alter operations to incorporate new technologies or processes, which may result in additional expenses and
adversely affect our operating results. We may also incur significant costs and utilize additional resources to comply with future
regulations related to climate-related disclosures.
We are also subject to other substantial regulation relating to environmental, health and safety matters, including
occupational health and safety, environmental protection, hazardous substance control, and waste management and disposal.
The failure to comply with such regulations could subject us to, among other things, fines and criminal liability. We may also
be required to incur significant costs to comply with these and future regulations, which may result in a material adverse effect
upon our business, financial condition and results of operation.
Changes in tax laws or exposures to additional tax liabilities could negatively impact the Company's operating results.
We are subject to income taxes, as well as taxes that are not income-based, in both the U.S. and jurisdictions outside of
the U.S. Our future effective tax rate could be unfavorably affected by numerous factors including a change in, or the
interpretation of, tax rules and regulations in the jurisdictions in which we operate (including changes in legislation currently
being considered), a change in our geographic earnings mix, and/or to the jurisdictions in which we operate, or a change in the
measurement of our deferred taxes. We are also subject to ongoing tax audits in various jurisdictions, and tax authorities may
disagree with certain positions we have taken and assess additional taxes.
INTELLECTUAL PROPERTY
Our business is dependent on technologies we license, and if we fail to maintain these licenses or license new technologies
and rights to particular nucleic acid sequences for targeted diseases in the future, we may be limited in our ability to develop
new products.
Our business is dependent on licenses from third parties for some of our key technologies. For example, our patented
TMA technology is based on technology we licensed from Stanford University. We anticipate that we will enter into new
licensing arrangements in the ordinary course of business to expand our product portfolio and access new technologies to
enhance our products and develop new products. Many of these licenses will provide us with exclusive rights to the subject
technology or disease marker. If our license with respect to any of these technologies or markers is terminated for any reason,
we may not be able to sell products that incorporate that technology. Similarly, we may lose competitive advantages if we fail
to maintain exclusivity under an exclusive license.
Our ability to develop additional diagnostic tests for diseases may depend on the ability of third parties to discover
particular sequences or markers and correlate them with disease, as well as the rate at which such discoveries are made. Our
ability to design products that target these diseases may depend on our ability to obtain the necessary rights from the third
parties that make any of these discoveries. In addition, there are a finite number of diseases and conditions for which our NAT
diagnostic assays may be economically viable. If we are unable to access new technologies or the rights to particular sequences
or markers necessary for additional diagnostic products on commercially reasonable terms, we may be limited in our ability to
develop new diagnostic products.
Our products and manufacturing processes may require access to technologies and materials that may be subject to patents
or other intellectual property rights held by third parties. Our business could be adversely affected if we are unable to obtain the
additional intellectual property rights necessary to commercialize our products.
Our business could be harmed if we are unable to protect our proprietary technology.
We have relied primarily on a combination of trade secrets, patents, copyrights, trademarks and confidentiality procedures
to protect our products and technology. Despite these precautions, unauthorized third parties may infringe, misappropriate or
otherwise violate our intellectual property, or copy or reverse engineer portions of our technology. The pursuit and assertion of
a patent right, particularly in areas like nucleic acid diagnostics and biotechnology, involve complex determinations and,
therefore, are characterized by substantial uncertainty. We do not know if current or future patent applications will be issued
with the full scope of the claims sought, if at all, or whether any patents that are issued will be challenged or invalidated. The
patents that we own or license could also be subjected to invalidation proceedings or similar disputes, and an unfavorable
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outcome could require us to cease using the related technology or to attempt to license rights to the technology from the
prevailing party. There is also a risk that intellectual property laws outside of the U.S. will not protect our intellectual property
rights to the same extent as intellectual property laws in the U.S. Even if our proprietary information is protected by patents or
otherwise, the initiation of actions to protect our proprietary information could be costly and divert the efforts and attention of
our management and technical personnel, and the outcome of such litigation is often uncertain. As a result of these
uncertainties, we could also elect to forego such litigation or settle such litigation without fully enforcing our proprietary rights.
In the absence of significant patent protection, we may be vulnerable to competitors who attempt to copy our products,
processes or technology. Additionally, rights provided by a patent are finite in time. Over the coming years, certain patents
relating to current products will expire in the U.S. and abroad thus allowing third parties to utilize certain of our technologies.
Our business could be harmed if we infringe upon the intellectual property rights of others.
There has been substantial litigation regarding patent and other intellectual property rights in the medical device,
diagnostic products and related industries. We are and have been involved in patent litigation and may in the future be subject
to further claims of infringement of intellectual property rights possessed by third parties. In connection with claims of patent
infringement, we may seek to enter into settlement and/or licensing arrangements. There is a risk in these situations that no
license will be available or that a license will not be available on reasonable terms. Alternatively, we may decide to litigate such
claims or to design around the technology. These actions could be costly and would divert the efforts and attention of our
management and technical personnel. As a result, any infringement claims by third parties or claims for indemnification by
customers resulting from infringement claims, whether or not proven to be true, may harm our business and prospects.
INDEBTEDNESS
We have a significant amount of indebtedness outstanding, which limits our operating flexibility, and could adversely affect
our operations and financial results and prevent us from fulfilling our obligations.
As of September 24, 2022, we had approximately $2.85 billion aggregate principal of indebtedness outstanding (exclusive
of additional funds that would be available to draw under our revolver). We also have other contractual obligations and deferred
tax liabilities, which as of September 24, 2022, are described under “Notes to Consolidated Financial Statements — Income
Taxes, and Non-cancelable Purchase Commitments.” This significant level of indebtedness and our other obligations may:
• make it more difficult for us to satisfy our obligations with respect to our outstanding indebtedness;
•
•
increase our vulnerability to general adverse economic and industry conditions, including increases in interest rates;
require us to dedicate a substantial portion of our cash flow from operations to interest and principal payments on our
indebtedness, which would reduce the availability of our cash flow to fund working capital, capital expenditures,
expansion efforts, strategic transactions and other general corporate purposes;
limit our flexibility in planning for, or reacting to, changes in our business and the markets in which we participate;
place us at a competitive disadvantage compared to our competitors that have less debt; and
limit our ability to borrow additional funds for working capital, capital expenditures, expansion efforts, strategic
transactions or other general corporate purposes.
•
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•
In addition, the terms of our financing obligations contain certain covenants that restrict our ability, and that of our
subsidiaries, to engage in certain transactions and may impair our ability to respond to changing business and economic
conditions, including, among other things, limitations on our ability to:
incur indebtedness or issue certain preferred equity;
pay dividends, repurchase our common stock, or make other distributions or restricted payments;
•
•
• make certain investments;
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agree to payment restrictions affecting the restricted subsidiaries;
sell or otherwise transfer or dispose of assets, including equity interests of our subsidiaries;
enter into transactions with our affiliates;
create liens;
designate our subsidiaries as unrestricted subsidiaries;
consolidate, merge or sell substantially all of our assets; and
use the proceeds of permitted sales of our assets.
Our credit facilities also require us to satisfy certain financial covenants. Our ability to comply with these provisions may
be affected by general economic conditions, political decisions, industry conditions and other events beyond our control. Our
failure to comply with the covenants contained in our credit facilities, including financial covenants, could result in an event of
default, which could materially and adversely affect our results of operations and financial condition.
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If there were an event of default under one of our debt instruments or a change of control, the holders of the defaulted debt
could cause all amounts outstanding with respect to that debt to be due and payable immediately and may be cross-defaulted to
other debt, including our outstanding notes. Our assets or cash flow may not be sufficient to fully repay borrowings under our
outstanding debt instruments if accelerated upon an event of default or a change of control, and there is no guarantee that we
would be able to repay, refinance or restructure the payments on such debt. See “Management’s Discussion and Analysis of
Financial Condition and Results of Operations-Liquidity and Capital Resources.”
We may not be able to generate sufficient cash flow to service all of our indebtedness and other obligations.
Our ability to make payments on and to refinance our indebtedness and to fund planned capital expenditures, strategic
transactions and expansion efforts will depend on our ability to generate cash in the future. This, to a certain extent, is subject to
general economic, financial, competitive, legislative, regulatory and other factors that are beyond our control. Our business may
not be able to generate sufficient cash flow from operations, and we cannot assure that future borrowings will be available to us
in amounts sufficient to enable us to pay our indebtedness as such indebtedness matures and to fund our other liquidity needs. If
this occurs, we will need to refinance all or a portion of our indebtedness on or before maturity, and there can be no assurance
that we will be able to refinance any of our indebtedness on commercially reasonable terms, or at all. We may need to adopt one
or more alternatives, such as reducing or delaying planned expenses and capital expenditures, selling assets, restructuring debt,
or obtaining additional equity or debt financing. These alternative strategies may not be affected on satisfactory terms, if at all.
Our ability to refinance our indebtedness or obtain additional financing, or to do so on commercially reasonable terms, will
depend on, among other things, our financial condition at the time, restrictions in agreements governing our indebtedness, and
other factors, including the condition of the financial markets and the markets in which we compete. If we do not generate
sufficient cash flow from operations, and additional borrowings, refinancings or proceeds from asset sales are not available to
us, we may not have sufficient cash to enable us to meet all of our obligations.
A significant portion of our indebtedness is subject to floating interest rates, which may expose us to higher interest
payments.
A significant portion of our indebtedness is subject to floating interest rates, which makes us more vulnerable in the event
of adverse economic conditions, increases in prevailing interest rates, or a downturn in our business. As of September 24, 2022,
approximately $1.5 billion aggregate principal of our indebtedness, which represented the outstanding principal under our credit
facilities, was subject to floating interest rates. We currently have a hedging arrangement (an interest rate swap that expires on
December 17, 2023) in place to partially mitigate the impact of higher interest rates. We cannot assure that we would be able to
extend this hedge at an attractive price and terms.
GENERAL RISK FACTORS
Provisions in our charter, bylaws, and indebtedness may have the effect of discouraging advantageous offers for our
business or common stock and limit the price that investors might be willing to pay in the future for shares of our common
stock.
Our charter, bylaws, and the provisions of the Delaware General Corporation Law include provisions that may have the
effect of discouraging or preventing a change of control. Our indebtedness also contains provisions which either accelerate or
require us to offer to repurchase the indebtedness at a premium upon a change of control. These provisions could limit the price
that our stockholders might receive in the future for shares of our common stock.
Our stock price is volatile.
The market price of our common stock has been, and may continue to be, highly volatile. We believe that a variety of
factors could cause the price of our common stock to fluctuate, perhaps substantially, including:
•
•
•
•
•
•
•
•
•
•
•
new, or changes in, recommendations, guidelines or studies that could affect the use of our products;
announcements and rumors of developments related to our business, including changes in reimbursement rates or
regulatory requirements, proposed and completed acquisitions, or the industry in which we compete;
published studies and reports relating to the comparative efficacy of products and markets in which we participate;
quarterly fluctuations in our actual or anticipated operating results and order levels;
general conditions in the U.S. or worldwide economy;
our stock repurchase program;
announcements of technological innovations;
new products or product enhancements by us or our competitors;
developments in patents or other intellectual property rights and litigation;
developments in relationships with our customers and suppliers;
the implementation of healthcare reform legislation and the adoption of additional reform legislation in the future; and
31
Table of Contents
•
the success or lack of success of integrating our acquisitions.
In addition, the stock market in general and the markets for shares of “high-tech” and life sciences companies, have
historically experienced extreme price fluctuations which have often been unrelated to the operating performance of affected
companies. Any such fluctuations in the future could adversely affect the market price of our common stock, and the market
price of our common stock may decline.
Item 1B. Unresolved Staff Comments
None.
32
Table of Contents
Item 2. Properties
We own and lease real property to support our business, including manufacturing, marketing, research and development,
logistical support and administration. The following lists those properties that we own or lease that we believe are material to
our business. We believe that we have adequate space for our anticipated needs and that suitable additional space will be
available at commercially reasonable prices as needed.
Material Properties Owned:
Newark, DE
Primary Use
DirectRay digital detector research and development and plate
manufacturing operations
Manchester, UK
Londonderry, NH
San Diego, CA
San Diego, CA
Material Properties
Leased:
Danbury, CT
Danbury, CT
Marlborough, MA
Administrative and supply chain operations
Manufacturing operations
Diagnostics headquarters, including administrative and
manufacturing operations
Diagnostics research and development, administrative and
manufacturing operations
Primary Use
Manufacturing facility
Manufacturing operations and
research and development
Headquarters, including research
and development, manufacturing
and distribution operations
Manufacturing operations
Marlborough, MA
Alajuela, Costa Rica Manufacturing facility
Manchester, England Manufacturing operations and
Ougrée, Belgium
research and development
Manufacturing operations and
research and development
Lease
Expiration
(fiscal year)
2026
2023
2025
2024
2028
2035
2032
Renewals
None
None
2, five-yr. periods
1, five-yr. period
2, five-yr. periods
None
None
We also lease various administrative and customer support centers throughout the world including in Brussels, Belgium,
Kerpen, and Berlin Germany, Madrid, Spain, and Shanghai and Beijing, China. In addition, we also lease space for smaller,
specialized research and development and manufacturing operations at various additional locations including Aix-en-Provence,
France, and Espoo, Finland.
Item 3. Legal Proceedings
For a discussion of legal matters as of September 24, 2022, please see Note 14 to our consolidated financial statements
entitled “Litigation and Related Matters,” which is incorporated by reference into this item.
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 Information. Our common stock is traded on the Nasdaq Global Select Market under the symbol “HOLX.”
Number of Holders. As of November 10, 2022, there were approximately 827 holders of record of our common stock,
including multiple beneficial holders at depositories, banks and brokers listed as a single holder in the street name of each
respective depository, bank or broker.
Dividend Policy. We have never declared or paid cash dividends on our capital stock, and we currently have no plans to
do so. Our current policy is to retain all of our earnings to finance future growth (including acquisitions), pay down our existing
indebtedness and repurchase our common stock. The existing covenants under certain of our credit facilities also place limits on
our ability to issue dividends and repurchase stock.
Recent Sales of Unregistered Securities. We did not sell unregistered securities during the fourth quarter of fiscal 2022.
Issuer's Purchases of Equity Securities
Total Number of
Shares
Purchased As
Part of Publicly
Announced
Plans or
Programs
(#) (2)
Average Price
Paid Per
Share As Part of
Publicly
Announced
Plans or
Programs
($) (2)
Maximum
Number (or
Approximate
Dollar Value) of
Shares That May
Yet Be Purchased
Under Our
Programs
(in millions)
($) (2)
Total Number of
Shares Purchased
(#) (1)
Average Price
Paid Per Share
($) (1)
1,120 $
2,245
552
3,917 $
70.14
70.95
68.42
70.36
— $
— $
565,047
1,984,671
71.44
67.86
2,549,718 $
68.66 $
324.7
284.4
1,000.0
1,000.0
Period of Repurchase
June 26, 2022 – July 23, 2022
July 24, 2022 – August 20, 2022
August 21, 2022 – September 24, 2022
Total
___________________________________
(1) For the majority of restricted stock units granted, the number of shares issued on the date that the restricted stock units vest
is net of the minimum statutory tax withholding requirements that we pay in cash to the appropriate tax authorities on
behalf of our employees. These repurchases of our common stock were to cover employee income tax withholding
obligations in connection with the vesting of restricted stock units under our equity incentive plans.
(2) On December 9, 2020, the Board of Directors authorized a share repurchase plan to repurchase up to $1.0 billion of the
Company's outstanding common stock, effective December 11, 2020. On September 22, 2022, the Board of Directors
authorized a new stock repurchase program, with a five-year term, to repurchase up to $1.0 billion of the Company’s
outstanding common stock, effective as of the close of trading on September 23, 2022. This new stock repurchase
authorization replaces the previous $1.0 billion authorization, which had approximately $150 million remaining as of
September 22, 2022.
34
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Stock Performance Graph
The following information shall not be deemed to be "filed" with the SEC nor shall the information be incorporated by
reference into any filings under the Securities Act, except to the extent that we specifically incorporate it by reference into a
document filed under the Securities Act or the Exchange Act.
The following graph compares cumulative total shareholder return on our common stock since September 30, 2017 with
the cumulative total return of the Standard & Poor’s 500 Index and the S&P Health Care Supplies Index. This graph assumes
the investment of $100 on September 30, 2017 in our common stock. Measurement points are the last trading day of each
respective fiscal year.
Item 6. Reserved
Not applicable.
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Item 7. Management's Discussion and Analysis of Financial Condition and Results of Operations
The following discussion and analysis should be read in conjunction with the Consolidated Financial Statements, the
information described under the caption “Risk Factors” in Part I, Item 1A of this Annual Report and our Special Note
Regarding Forward-Looking Statements at the outset of this Annual Report.
OVERVIEW
We are a developer, manufacturer and supplier of premium diagnostics products, medical imaging systems and surgical
products focused on women's health and well-being through early detection and treatment. We sell and service our products
through a combination of direct sales and service personnel and a network of independent distributors and sales representatives.
We operate in four segments: Diagnostics, Breast Health, GYN Surgical and Skeletal Health.
Through our Diagnostics segment, we offer a wide range of diagnostic products, which are used primarily to aid in the
screening and diagnosis of human diseases. Our primary Diagnostics products include our molecular diagnostic assays, which
run on our advanced instrumentation systems (Panther, Panther Fusion and Tigris), our ThinPrep cytology system, and the
Rapid Fetal Fibronectin Test. Our Aptima family of molecular diagnostic assays is used to detect, among other things, the
infectious microorganisms that cause common sexually transmitted diseases, or STDs, such as chlamydia and gonorrhea, or
GTGC; certain high-risk strains of human papillomavirus, or HPV; Trichomonas vaginalis, the parasite that causes
trichomoniasis; Mycoplasma genitalium; and Herpes Simplex viruses 1 and 2. We also offer viral load tests for the quantitation
of Hepatitis B virus, Hepatitis C virus, human immunodeficiency virus, and human cytomegalo virus for use on our Panther
instrument system. In addition, we offer bacterial vaginosis and candida vaginitis assays for the diagnosis of vaginitis, a
common and complex ailment affecting millions of women a year. Our assay portfolio also includes diagnostic tests for a range
of acute respiratory infections, including SARS-CoV-2, various strains of influenza and parainfluenza, and respiratory syncytial
virus that are run on the Panther Fusion system, a field upgradeable instrument addition to the base Panther system. In response
to the COVID-19 pandemic, we developed and launched the Aptima SARS-CoV-2 assay and the Aptima SARS-CoV-2/Flu
assay (each of which runs on our standard Panther system) and the Panther Fusion SARS-CoV-2 assay (which runs on our
Panther Fusion system). In May 2022, we CE-marked two new molecular assays, Panther Fusion EBV Quant assay for
quantitation of Epstein-Barr virus, and the Panther Fusion BKV Quant assay for quantitation of the BK virus. These two new
assays are the first quantitative real-time PCR assays on the Panther Fusion system. These assays, along with the Aptima CMV
Quant assay already available in Europe, expand our Panther Fusion menu of transplant monitoring assays. The ThinPrep
System is primarily used in cytology applications, such as cervical cancer screening, and the Rapid Fetal Fibronectin Test
assists physicians in assessing the risk of pre-term birth. We also generate service revenues from our CLIA-certified laboratory
for testing related to breast cancer and all metastatic cancers.
Our Breast Health segment offers a broad portfolio of solutions for breast cancer care primarily in the areas of radiology,
breast surgery, pathology and treatment. These solutions include 3D digital mammography systems, image analytics software
utilizing artificial intelligence, reading workstations, ultrasound imaging, minimally invasive breast biopsy guidance systems,
breast biopsy site markers, localization, specimen radiology, connectivity solutions and breast conserving surgery products. Our
most advanced breast imaging platforms, Selenia Dimensions and 3Dimensions, utilize tomosynthesis to produce 3D images
that show multiple contiguous slice images of the breast, which we refer to as the Genius 3D Mammography exam.
Our GYN Surgical products include our NovaSure Endometrial Ablation System, or NovaSure, our MyoSure
Hysteroscopic Tissue Removal System, or MyoSure, our Fluent Fluid Management system, or Fluent, our Acessa ProVu
laparoscopic radiofrequency ablation system, or Acessa, as well as our CoolSeal vessel sealing portfolio and our JustRight
surgical stapler. The NovaSure portfolio is comprised of the NovaSure CLASSIC and NovaSure ADVANCED devices and
most recently, the NovaSure portfolio V5 device for the treatment of abnormal uterine bleeding. The MyoSure suite of devices
offers four options to provide incision-less removal of fibroids, polyps, and other pathology within the uterus. The Fluent
system is a fluid management system that provides liquid distention during diagnostic and operative hysteroscopic procedures.
The Acessa system is a fully integrated system that uses laparoscopic ultrasound, guidance mapping and radio frequency
ablation to treat nearly all types of fibroids. The CoolSeal portfolio includes the Trinity, Reveal, and Mini advanced bipolar
vessel sealing devices. The JustRight 5 mm stapler features a smaller instrument profile and is used for laparoscopic general
and pediatric surgery.
Our Skeletal Health segment's products includes the Horizon DXA, a dual energy x-ray system, which evaluates bone
density and performs body composition assessments, and the Fluoroscan Insight FD mini C-arm, which assists in performing
minimally invasive orthopedic surgical procedures on a patient's extremities, such as the hand, wrist, knee, foot, and ankle.
Unless the context otherwise requires, references to we, us, Hologic or our company refer to Hologic, Inc. and its
consolidated subsidiaries.
Supply Chain Considerations
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The current worldwide supply chain shortages and constraints are impacting our ability to obtain certain critical raw
materials and components used primarily in our Breast Health capital equipment products. The supply chain shortages and
disruptions primarily affecting our Breast Health manufacturing lines are related to electronic components, primarily
semiconductor chips. We are dependent on a small number of semiconductor manufacturers and their allocation of chips to us.
Based on our current understanding of their allocation of chips to us we expect we will be able to increase production on a
sequential quarterly basis throughout fiscal 2023. If such allocation does not meet our expectations or we are not able to obtain
alternative sources of chips, we believe we will not be able to manufacture sufficient quantities of our capital equipment
products, primarily 3D Dimension systems, Trident specimen radiography systems, Affirm Prone biopsy systems and Brevera
systems to meet customer demand. As a result, if we are unable to obtain sufficient quantities of chips, sales of these products
may decline or will not increase in fiscal 2023 compared to fiscal 2022 levels. In addition, the prices of raw materials and
components, as well as freight, have been rising and continued supply chain shortages could increase the costs further. These
factors may result in a lower gross margin for Breast Health in fiscal 2023 for our affected products. Our procurement team has
and will continue to expend significant time and resources to try to secure sufficient quantities to meet demand.
Acquisitions
The following sets forth a description of certain of our acquisitions we have completed in our last two fiscal years:
Bolder Surgical
On November 29, 2021, we completed the acquisition of Bolder Surgical Holdings, Inc., or Bolder, for a purchase
price of $160.1 million. Bolder, located in Louisville, Colorado, is a developer and manufacturer of energy vessel sealing
surgical devices used in both laparoscopic and open procedures. Based on our preliminary valuation, we allocated $96.7 million
of the purchase price to the value of intangible assets and $68.8 million to goodwill. The allocation of the purchase price is
preliminary as we continue to gather information supporting the valuation of the acquired assets and liabilities. Bolder's results
of operations are reported in our GYN Surgical segment.
Mobidiag
On June 17, 2021, we completed the acquisition of Mobidiag Oy, or Mobidiag, for a purchase price of $729.6 million.
Mobidiag, located in Finland, manufactures molecular diagnostic solutions for gastrointestinal infections, antimicrobial
resistance management and other infections. We also acquired $66.1 million of debt, which was paid off in fiscal 2022. Based
on our valuation, we allocated $399.9 million of the purchase price to the value of intangible assets and $427.7 million to
goodwill. This acquisition expands our molecular diagnostics portfolio into the near-patient testing market. Mobidiag's results
of operations are reported in our Diagnostics segment.
Biotheranostics
On February 22, 2021, we completed the acquisition of Biotheranostics, Inc., or Biotheranostics, for a purchase price
of $231.3 million. Biotheranostics, located in San Diego, California, manufactures molecular diagnostic tests that support
physicians in the treatment of breast cancer and all metastatic cancers and performs lab testing procedures at its CLIA-certified
laboratory. Based on our valuation, we allocated $162.4 million of the purchase price to the value of intangible assets and $80.9
million to goodwill. Biotheranostics' results of operations are included in our Diagnostics segment, and its revenues are reported
within Service and Other Revenue in our Consolidated Statements of Income.
Diagenode
On March 1, 2021, we completed the acquisition of Diagenode SA, or Diagenode, for a purchase price of $155.1 million.
Diagenode, located in Belgium, is a developer and manufacturer of molecular diagnostic assays based on polymerase chain
reaction (PCR) technology to detect infectious diseases of bacterial, viral or parasite origin. Based on our valuation, we
allocated $79.0 million of the purchase price to the value of intangible assets and $83.5 million to goodwill. Diagenode's results
of operations are included in our Diagnostics segment.
Somatex Medical Technologies
On December 30, 2020, we completed the acquisition of Somatex Medical Technologies GmbH, or Somatex, for a
purchase price of $62.9 million. Somatex, located in Germany, is a manufacturer of biopsy site markers, including the Tumark
product line of tissue markers, which we distributed in the U.S. prior to the acquisition. Somatex' results of operations are
included in our Breast Health segment.
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Table of Contents
RESULTS OF OPERATIONS
Fiscal Year Ended September 24, 2022 Compared to Fiscal Year Ended September 25, 2021
Product Revenues
Product Revenues
Diagnostics
Breast Health
GYN Surgical
Skeletal Health
September 24, 2022
Fiscal Years Ended
September 25, 2021
Change
Amount
% of Total
Revenue
Amount
% of Total
Revenue
Amount
%
$
$
2,924.6
680.5
521.4
64.7
4,191.2
60.1 % $
14.0 %
10.7 %
1.3 %
86.2 % $
3,596.1
815.1
486.8
69.3
4,967.3
63.9 % $
14.5 %
8.6 %
1.2 %
88.2 % $
(671.5)
(134.6)
34.6
(4.6)
(776.1)
(18.7) %
(16.5) %
7.1 %
(6.6) %
(15.6) %
We had a decrease in product revenue of 15.6% in fiscal 2022 compared to fiscal 2021. This decrease was primarily due
to the decline in revenues in the Diagnostics business as a result of lower COVID-19 assay sales, a decrease in Breast Health
revenue, which we primarily attribute to supply chain constraints, and to a lesser extent the negative effect from the unfavorable
foreign currency exchange impact of the strengthened U.S. dollar against a number of currencies. The decrease in product
revenues in fiscal 2022 compared to fiscal 2021 was partially offset by an increase in GYN Surgical product revenue due to an
increase in sales volume of these products which we attribute to a recovery of elective procedures as COVID-19 restrictions
eased, as well as an increase from our recent acquisitions.
Diagnostics product revenues decreased 18.7% in fiscal 2022 compared to fiscal 2021 primarily due to decreases in
Molecular Diagnostics of $656.4 million and a decrease in blood-screening of $15.8 million, partially offset by an increase in
Cytology and Perinatal revenue of $0.7 million. While we divested our blood screening business in the second quarter of fiscal
2017, we continue to provide long-term access to Panther instrumentation and certain supplies to the purchaser of that business.
Molecular Diagnostics product revenue was $2,427.5 million in fiscal 2022 compared to $3,083.9 million in fiscal 2021. The
decrease was primarily attributable to a reduction of $729.0 million in sales our two SARS-CoV-2 assays (primarily the Aptima
SARS-CoV-2 assay and to a lesser extent the Panther Fusion SARS-CoV-2 assay) to $1,430.5 million in fiscal 2022 compared
to $2,159.5 million in fiscal 2021 primarily due to lower demand from an improvement in the COVID-19 pandemic and, to a
lesser extent, the impact of at-home testing alternatives and lower average selling prices on a worldwide basis . We also had a
decrease in Panther and Panther Fusion instrument sales in fiscal 2022 compared to fiscal 2021 as sales in fiscal 2021 were
higher primarily due to the COVID-19 pandemic as customers expanded their Covid assay testing capacity. These decreases
were partially offset by an increase of $53.6 million in our Aptima assays and STD collection kits (exclusive of our SARS-
CoV-2 assay), which primarily consist of our CTGC, Bacterial Vaginosis, and CV Candida assays, on a worldwide basis as
volumes increased, partially offset by lower HPV assay volumes and a decrease in average selling prices. In addition, we had an
increase of $32.6 million in worldwide sales of our Quant Viral assays and Fusion respiratory products in the current fiscal
year. The inclusion of Diagenode and Mobidiag products contributed $13.3 million of incremental product revenue in the
current fiscal year. We also experienced a decrease in revenue from international sales denominated in foreign currencies from
the unfavorable foreign currency exchange impact of the strengthened U.S. dollar against a number of currencies. We expect
that sales of our COVID-19 assays will continue to decline in fiscal 2023 compared to the current fiscal year as the pandemic
recedes and given the continued distribution of vaccines and boosters.
Breast Health product revenues decreased 16.5% in fiscal 2022 compared to fiscal 2021 primarily due to a decrease in
volumes of our digital mammography systems, primarily 3D Dimensions systems, related software and workflow products,
Affirm biopsy systems and Brevera biopsy systems. The decrease in volume was primarily driven by supply chain constraints
related to electronic components, primarily semiconductor chips, that impacted our ability to manufacture sufficient quantities
to meet customer demand. We continue to have strong back orders for our capital equipment. These decreases were partially
offset by an increase in average selling prices, as well as an increase in sales of our interventional breast solutions products,
primarily driven by ATEC and Brevera disposables. We also experienced a decrease in revenue from international sales
denominated in foreign currencies from the unfavorable foreign currency exchange impact of the strengthened U.S. dollar
against a number of currencies.
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GYN Surgical product revenues increased 7.1% in fiscal 2022 compared to fiscal 2021, primarily due to increases in the
sales volume of our Fluent Fluid Management products, Bolder products (comprised of CoolSeal vessel sealing devices and
JustRight surgical staplers), MyoSure system sales and Acessa ProVu systems. These increases were partially offset by
decreases in NovaSure system sales. We also experienced a decrease in revenue from international sales denominated in foreign
currencies from the unfavorable foreign currency exchange impact of the strengthened U.S. dollar against a number of
currencies.
Skeletal Health product revenues decreased 6.6% in fiscal 2022 compared to fiscal 2021 primarily due to a decrease in
sales volume of our Horizon DXA systems and Insight FD Fluoroscan systems. We attribute this sales volume decrease largely
to supply chain constraints. We also experienced a decrease in revenue from international sales denominated in foreign
currencies from the unfavorable foreign currency exchange impact of the strengthened U.S. dollar against a number of
currencies.
Product revenues by geography as a percentage of total revenues were as follows:
United States
Europe
Asia-Pacific
Rest of world
Years ended
September 24,
2022
September 25,
2021
69.4 %
19.7 %
7.7 %
3.2 %
100.0 %
68.3 %
21.9 %
6.7 %
3.1 %
100.0 %
The percentage of product revenue derived from the U.S. and Asia-Pacific increased while Europe decreased, which we
primarily attribute to a steeper decline in SARS-CoV-2 assay sales in Europe compared to the U.S., partially offset by an
increase in HIV assay sales in Africa, and an increase in SARS-CoV-2 assay sales in Australia and New Zealand. The
percentage of product revenue increased in Asia-Pacific is primarily due to an increase in volume of ThinPrep and HPV assays
in China. In addition, the strengthening of the U.S. dollar against a number of currencies contributed to the increase in the
percentage of revenue derived from the U.S. compared to revenue derived from the other geographic regions.
Service and Other Revenues
Years Ended
September 24, 2022
September 25, 2021
Change
Amount
% of
Total
Revenue
Amount
% of
Total
Revenue
Amount
%
Service and Other Revenues
$
671.6
13.8 % $
665.0
11.8 % $
6.6
1.0 %
Service and other revenues are primarily comprised of revenue generated from our field service organization to provide
ongoing service, installation and repair of our products. The majority of these revenues are generated within our Breast Health
segment. Service and other revenues increased 1.0% in fiscal 2022 compared to fiscal 2021 primarily due to an increase in
Breast Health service contract revenue as the Breast Health business continued to convert a high percentage of our installed
base of digital mammography systems to service contracts upon expiration of the warranty period, as well as additions from our
distributor acquisitions. This increase was partially offset by a decrease in installation and training services that are provided
with capital product sales as a result of lower unit sales in the current fiscal year. In our Diagnostics business, lab testing
revenue from the inclusion of our Biotheranostics acquisition in the second quarter of fiscal 2021, increased $35.9 million in the
current year. This was offset by a decrease in royalty revenue of $46.2 million from Grifols, S.A., or Grifols, related to
licensing our intellectual property to our COVID-19 assays for their sale in Spain, as the contract expired in December 2021.
Cost of Product Revenues
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Cost of Product Revenues
Amortization of Acquired
Intangible Assets
Impairment of Acquired
Intangible Assets and Equipment
** Percentage not meaningful
September 24, 2022
Years Ended
September 25, 2021
Change
Amount
% of Product
Sales
Amount
% of Product
Sales
Amount
%
$
1,166.1
27.8 % $
1,205.1
24.3 % $
(39.0)
(3.2) %
295.7
7.1 %
276.7
5.5 %
19.0
6.9 %
17.4
1,479.2
$
0.4 %
35.3 % $
—
1,481.8
— %
29.8 % $
17.4
(2.6)
**
(0.2) %
Product gross margin was 64.7% in fiscal 2022 compared to 70.2% in fiscal 2021.
Cost of Product Revenues. The cost of product revenues as a percentage of product revenues was 27.8% in the current
year compared to 24.3% in the prior year. Cost of product revenues as a percentage of revenue increased in fiscal 2022
primarily due to a decrease in sales of our SARS-CoV-2 assays, which have higher gross margins compared to our other
Diagnostic products, and comprised 34.1% and 43.5% of total product revenue in fiscal 2022 and fiscal 2021, respectively.
Diagnostics' product costs as a percentage of revenue increased in fiscal 2022 compared to fiscal 2021 primarily due to
lower sales of our SARS-CoV-2 assays, a slight decline in average selling prices of certain assays, an increase in inventory
reserves, higher field service costs for our expanded instrument installed base and higher freight charges internationally,
partially offset by lower sales of instruments, which carry low margins, and an increase in sales of our Aptima and Quant Viral
assays.
Breast Health’s product costs as a percentage of revenue increased in fiscal 2022 compared to fiscal 2021 primarily due to
the impact of the COVID-19 pandemic on the supply chain resulting in lower sales volumes of our higher margin products,
reduced manufacturing utilization and higher prices of raw materials and components, partially offset by a slight increase in
average selling prices of our 3Dimensions systems and related workflow products.
GYN Surgical’s product costs as a percentage of revenue increased in fiscal 2022 compared to fiscal 2021 primarily due
to product mix of higher volumes of lower margin products, mostly attributable to sales of our Fluent Fluid Management
systems, Bolder products (comprised of CoolSeal vessel sealing devices and JustRight surgical staplers) and Acessa ProVu
systems.
Skeletal Health’s product costs as a percentage of revenue increased in fiscal 2022 compared to fiscal 2021 primarily due
to increased costs for our Horizon DXA systems workstation upgrades and lower sales volumes of our Horizon DXA and
Insight FD systems primarily due to supply chain constraints, partially offset by a slight increase in average selling prices of our
Horizon DXA and Insight FD systems.
Amortization of Acquired Intangible Assets. Amortization of intangible assets included in cost of product revenues
relates to acquired developed technology, which is generally amortized over its estimated useful life of between 5 and 15 years
using a straight-line method or, if reliably determinable, based on the pattern in which the economic benefits of the assets are
expected to be consumed. Amortization expense increased in fiscal 2022 compared to fiscal 2021 primarily due to intangible
assets acquired in the Mobidiag, Biotheranostics, Diagenode and Bolder acquisitions as well as accelerated amortization related
to shortening the life of certain intangible assets acquired in the acquisitions of SuperSonic Imagine SA, or SSI and Faxitron.
This was partially offset by lower amortization of intangible assets acquired in the Cytyc acquisition which reduces over time.
Impairment of Intangible Assets and Equipment. As discussed in Note 2 to the consolidated financial statements, we
determined that certain developed technology assets acquired in the Focal and Faxitron acquisitions were impaired as a result of
decisions to no longer sell certain low-volume products. As a result, we recorded an impairment charge of $17.4 million to
write-off these developed technology assets in fiscal 2022.
Cost of Service and Other Revenues
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Years Ended
September 24, 2022
September 25, 2021
Change
Amount
% of Service
and Other
Revenues
Amount
% of Service
and Other
Revenues
Amount
%
Cost of Service and Other
Revenues
$
386.2
57.5 % $
354.7
53.3 % $
31.5
8.9 %
Service and other revenues gross margin was 42.5% in fiscal 2022 compared to 46.7% in fiscal 2021. The decrease in
gross margin was primarily due to a decrease in royalty revenue from Grifols related to licensing our intellectual property
related to our COVID-19 assays for their sale in Spain, which had a high margin. This decrease is partially offset by the
inclusion of lab testing revenue from Biotheranostics, which has higher margins than our legacy service business and an
increase in Breast Health service contract revenue which benefited gross margin as service contract revenue has higher margins
compared to revenue from spare parts, installation and training.
Operating Expenses
Operating Expenses
Research and development
$
Selling and marketing
General and administrative
Amortization of acquired
intangible assets
Impairment of acquired
intangible assets and
equipment
Contingent consideration—
fair value adjustments
Restructuring and divestiture
charges
** Percentage not meaningful
283.4
630.3
407.7
45.2
27.7
September 24, 2022
September 25, 2021
Change
Amount
% of Total
Revenue
Amount
% of Total
Revenue
Amount
%
Years Ended
5.8 % $
13.0 %
8.4 %
276.3
561.2
433.2
4.9 % $
10.0 %
7.7 %
7.1
69.1
(25.5)
2.6 %
12.3 %
(5.9) %
0.9 %
42.2
0.7 %
3.0
7.1 %
0.6 %
—
— %
27.7
(39.5)
(0.8) %
(6.7)
(0.1) %
(32.8)
**
**
2.4
— %
9.3
$
1,357.2
27.9 % $
1,315.5
0.2 %
23.4 % $
(6.9)
41.7
(74.2) %
3.2 %
Research and Development Expenses. Research and development expenses increased 2.6% in fiscal 2022 compared to
fiscal 2021 primarily due to the inclusion of incremental expenses from the Mobidiag, Biotheranostics, Diagenode and Bolder
acquisitions aggregating $26.7 million. Partially offsetting this increase was the prior year period inclusion of a $7.0 million
charge related to the purchase of intellectual property in Breast Health that has no future alternative use, the reversal of a $5.2
million research and development tax credit reserve related to the SSI acquisition in fiscal 2022, a higher credit of $3.2 million
recorded to research and development expenses in fiscal 2022 from the Biomedical Advanced Research and Development
Authority (BARDA) in connection with a grant to obtain FDA approval of our SARS-CoV-2 assays and develop sampling
pooling capability and other enhancements to our SARS-CoV-2 assays, a reduction in spend to implement the European
Medical Device Regulation (MDR) and In Vitro Diagnostic Regulation (IVDR) requirements, and lower bonus and expense
under our deferred compensation plan. At any point in time, we have a number of different research projects and clinical trials
being conducted and the timing of these projects and related costs can vary from period to period.
Selling and Marketing Expenses. Selling and marketing expenses increased 12.3% in fiscal 2022 compared to fiscal
2021 primarily due to increased spend on marketing initiatives including our sponsorship of the Women's Tennis Association
and our Super Bowl commercial, the inclusion of expenses from the Mobidiag, Biotheranostics, Diagenode and Bolder
acquisitions aggregating $28.9 million and an increase in travel, meetings and trade shows that were lower in the prior year
primarily due to canceled or curtailed events as a result of the COVID-19 pandemic. Partially offsetting these increases in the
current year is a decrease in Breast Health commissions due to lower revenue, a decrease in consulting spend and lower bonus.
General and Administrative Expenses. General and administrative expenses decreased 5.9% in fiscal 2022 compared to
fiscal 2021 primarily due to a decrease in acquisition transactions costs of $19.7 million, lower bonus and expense from our
deferred compensation plan, a decrease in bad debt expense of $10.1 million, lower litigation and settlement costs, lower
41
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integration costs and a reduction in consulting spend. Partially offsetting these decreases was the inclusion of incremental
expenses from the Mobidiag, Biotheranostics, Diagenode and Bolder acquisitions aggregating $13.1 million, an increase in
charitable donations of $9.0 million, an increase in non-income tax charges, higher information systems infrastructure project
spend, an increase in tax and accounting projects and increased travel. In addition, in fiscal 2021 we recorded a $3.5 million
credit related to services provided under the transition services agreement for the Cynosure medical aesthetics business we sold
in fiscal 2020.
Amortization of Acquired Intangible Assets. Amortization of intangible assets results from customer relationships, trade
names and distributor relationships related to our acquisitions. These intangible assets are generally amortized over their
estimated useful lives of between 5 and 30 years using a straight-line method or, if reliably determinable, based on the pattern in
which the economic benefits of the assets are expected to be consumed utilizing expected undiscounted future cash flows.
Amortization expense increased 7.1% in fiscal 2022 compared to fiscal 2021 primarily due to increases from recent
acquisitions, partially offset by assets from older acquisitions becoming fully amortized.
Impairment of Intangible Assets and Equipment. As discussed in Note 2 to the consolidated financial statements, we
recorded an impairment charge of $27.7 million during fiscal 2022 to record our only IPR&D asset to fair value. The reduction
in fair value was due to an increase in the discount rate from higher interest rates, a reduction in forecasted revenues and timing
of completing the project.
Contingent Consideration Fair Value Adjustments. In connection with the acquisition of Acessa, we are obligated to
make contingent earn-out payments. The payments are based on achieving incremental revenue growth over a three-year period
ending annually in December of each 2021, 2022, and 2023. As of the acquisition date for Acessa, we recorded a contingent
consideration liability for the estimated fair value of the amount we expected to pay to the former shareholders of the acquired
business. This liability is not contingent on future employment, and we recorded our estimate of the fair value of the contingent
consideration liability utilizing the Monte Carlo simulation based on future revenue projections of Acessa, comparable
company revenue growth rates, implied volatility and applying a risk adjusted discount rate. Increases or decreases in the fair
value of contingent consideration liabilities can result from the passage of time, changes in discount rates, and changes in the
timing, probabilities and amount of revenue estimates. In the current year, we recorded a gain of $39.5 million to decrease the
liability to its fair value. The reduction in fair value was primarily due to a decrease in forecasted revenues over the
measurement period and to a lesser extent an increase in interest rates. In 2021, we recorded a gain of $6.7 million primarily
due to a decrease in forecasted revenues over the measurement period.
Restructuring and Divestiture Charges. We have implemented various cost reduction initiatives to align our cost
structure with our operations and related to integration activities. These actions have primarily resulted in the termination of
employees. As a result, we recorded charges of $2.4 million in fiscal 2022 and $9.3 million in fiscal 2021, primarily related to
severance benefits. For additional information, please refer to Note 6 to our consolidated financial statements.
Interest Expense
September 24, 2022
September 25, 2021
Change
Amount
Amount
Amount
%
Years Ended
Interest Expense
$
(95.1) $
(93.6) $
(1.5)
1.6 %
Interest expense in fiscal 2022 and 2021 consists primarily of the cash interest costs and the related amortization of the
debt discount and deferred issuance costs on our outstanding debt. Interest expense in fiscal 2022 increased compared to fiscal
2021 primarily due to an increase in the variable interest rate under our 2021 Credit Agreement partially offset by lower interest
rate swap expense as our hedged benchmark interest rate increased throughout the year, lower debt refinancing costs of $4.0
million, and lower interest on our Senior Notes due to issuing our 2029 Senior Notes and paying off our 2025 Senior Notes in
the prior year, which had a higher fixed rate.
Debt Extinguishment Loss
Debt Extinguishment Loss
$
(0.7) $
(21.6) $
20.9
September 24, 2022
September 25, 2021
Change
Amount
Amount
Amount
Years Ended
%
(100.0) %
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Table of Contents
In the first quarter of fiscal 2022, we entered into a Refinancing Amendment No. 2 to the 2021 Credit Agreement with
Bank of America, N.A. The proceeds were used to pay off the term loan outstanding under the 2018 Credit Agreement. In
connection with this transaction we recorded a debt extinguishment charge of $0.7 million. In the first quarter of fiscal 2021, we
completed a private placement of $950 million aggregate principal amount of our 2029 Senior Notes. The proceeds under the
2029 Senior Notes offering, together with available cash, were used to redeem our 2025 Senior Notes in the same principal
amount. In connection with this transaction, we recorded a debt extinguishment loss of $21.6 million in the first quarter of fiscal
2021.
Other Income (Expense), net
Other Income (Expense), net
$
30.9 $
(5.4) $
36.3
September 24, 2022
September 25, 2021
Change
Amount
Amount
Amount
Years Ended
%
(672.2) %
In fiscal 2022, this account primarily consisted of net foreign currency exchange gains of $48.5 million, primarily from
settling forward foreign currency hedging transactions and mark-to-market of outstanding foreign currency contracts, and a
$2.4 million gain on life insurance proceeds as a result of the death of a former employee, partially offset by a loss of $12.2
million from the change in cash surrender value of life insurance contracts related to our deferred compensation plan primarily
driven by stock market losses, a $4.0 million impairment charge of an equity investment and a charge of $4.3 million to write-
off an equity method investment acquired in the Mobidiag acquisition.
In fiscal 2021, this account primarily consisted of a net foreign currency exchange loss of $17.1 million, partially driven
by the mark-to-market and settling of outstanding foreign currency contracts, and a charge of $1.8 million for the write-off of
an equity investment, partially offset by a gain of $13.4 million on the cash surrender value of life insurance contracts related to
our deferred compensation plan driven by prior year stock market gains.
Provision for Income Taxes.
Provision for Income Taxes
$
286.2 $
491.4 $
(205.2)
41.8 %
September 24, 2022
September 25, 2021
Change
Amount
Amount
Amount
%
Years Ended
Our effective tax rate for fiscal 2022 was a provision of 18.0%. The effective tax rate was lower than the U.S. statutory
tax rate primarily due to the impact of the U.S. deduction for foreign derived intangible income, reserve releases resulting from
statute of limitations expirations and favorable audit settlements (net of reserve additions for uncertain tax positions), the
geographic mix of income earned by the Company's international subsidiaries, which are taxed at rates lower than the U.S.
statutory tax rate and a tax benefit related to an internal restructuring, partially offset by state income taxes and the global
intangible low-taxed income inclusion.
Our effective tax rate for fiscal 2021 was a provision of 20.8%. The effective tax rate was lower than the U.S. statutory
tax rate primarily due to the impact of the U.S. deduction for foreign derived intangible income and the geographic mix of
income earned by our international subsidiaries, which are taxed at rates lower than the U.S. statutory tax rate, partially offset
by state income taxes and the global intangible low-taxed income inclusion.
Segment Results of Operations
We operate in four segments: Diagnostics, Breast Health, GYN Surgical, and Skeletal Health. The accounting policies of
the segments are the same as those described in the footnotes to the accompanying consolidated financial statements contained
in Item 15 of this Annual Report. We measure segment performance based on total revenues and operating income (loss).
Revenues from product sales of each of these segments are described in further detail above. The discussion that follows is a
summary analysis of total revenues and the primary changes in operating income or loss by segment.
Diagnostics
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Table of Contents
Total Revenues
Operating Income
Years Ended
September 24, 2022
September 25, 2021
Change
Amount
Amount
Amount
%
$
$
3,018.5
1,359.4
$
$
3,695.0
2,140.1
$
$
(676.5)
(780.7)
(18.3) %
(36.5) %
Operating Income as a % of Segment Revenue
45.0 %
57.9 %
Diagnostics revenues, as discussed above, decreased in fiscal 2022 compared to fiscal 2021 primarily due to a decrease in
sales of our SARS-CoV-2 assays and a decrease in royalty revenue from Grifols related to licensing our intellectual property of
our COVID-19 assays for their sale in Spain, partially offset by revenue from recent acquisitions and an increase in sales of our
Aptima and Quant Viral assays.
Operating income for this business segment decreased in fiscal 2022 compared to fiscal 2021 primarily due to a decrease
in gross profit from lower revenues and an increase in operating expenses. Gross margin was 67.1% in the current year
compared to 73.2% in the prior year. The decrease in gross margin was primarily due to decreased sales of our SARS-CoV-2
assays which have a higher margin, an increase in intangible asset amortization expense from recent acquisitions, lower Grifols
license revenue, an increase in inventory reserves, higher field service costs for our expanded install bases and an increase in
freight internationally, partially offset by the inclusion of Biotheranostics lab testing revenue which has a higher gross margin
than our legacy businesses.
Operating expenses increased in fiscal 2022 compared to fiscal 2021 primarily due to the IPR&D charge of $27.7 million,
the inclusion of operating expenses from the Biotheranostics, Mobidiag, and Diagenode acquisitions in the amount of $67.6
million, an increase in allocated advertising and charitable contributions, an increase in marketing initiatives, trade shows,
meetings and travel expenses. These increases were partially offset by lower acquisition transaction costs, lower bonus and
expense from our deferred compensation plan, lower integration costs, lower bad debt expense, lower MDR/IVDR
implementation costs, and a higher BARDA credit of $3.2 million in the current year.
Breast Health
Total Revenues
Operating Income
Years Ended
September 24, 2022
September 25, 2021
Change
Amount
Amount
Amount
%
$
$
1,227.8
183.2
$
$
1,352.2
284.2
$
$
(124.4)
(101.0)
(9.2) %
(35.5) %
Operating Income as a % of Segment Revenue
14.9 %
21.0 %
Breast Health revenues decreased in fiscal 2022 compared to fiscal 2021 primarily due to a decrease of $134.6 million in
product revenue as discussed above, partially offset by an increase of $10.1 million in service and other revenue. The increase
in service revenue is primarily due to an increase in service contract revenue as the Breast Health business continued to convert
a high percentage of our installed base of digital mammography systems to service contracts upon expiration of the warranty
period.
Operating income for this business segment decreased in fiscal 2022 compared to fiscal 2021 primarily due to a decrease
in product sales and service gross profit, partially offset by a decrease in operating expenses. Gross margin was 51.9% in the
current year compared to 56.4% in the prior year. The decrease in gross margin is primarily due to lower volumes of capital
equipment sales, the reduced manufacturing utilization from supply chain shortages, higher costs for raw materials and
components, an intangible asset charge of $17.4 million related to certain developed technology assets our Faxitron and Focal
acquisitions and an increase in intangible asset amortization expense.
Operating expenses decreased in fiscal 2022 compared to fiscal 2021 primarily due to the reversal of a research and
development credit reserve related to the SSI acquisition, a decrease in compensation and commissions from lower sales and
sales force headcount, lower bad debt expense, lower bonus and expense from our deferred compensation plan, lower MDR/
IVDR implementation costs, lower legal expenses, and a reduction of restructuring charges. These decreases are partially offset
by an increase in allocated advertising and charitable contributions, higher marketing initiatives, an increase in travel and higher
trade shows and seminars.
GYN Surgical
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Total Revenues
Operating Income
Operating Income as a % of Segment Revenue
September 24, 2022
September 25, 2021
Change
Amount
Amount
Amount
%
Years Ended
$
$
522.9
104.9
$
$
20.1 %
488.1
58.9
$
$
12.1 %
34.8
46.0
7.1 %
78.1 %
GYN Surgical revenues increased in fiscal 2022 compared to fiscal 2021 due to the increase in product revenues
discussed above.
Operating income for this business segment increased in fiscal 2022 compared to fiscal 2021 primarily due to an increase
in gross profit from higher revenues and a decrease in operating expenses. Gross margin was 59.2% in the current year,
compared to 61.0% in the prior year. The decrease in gross margin was primarily due to product mix as we sold more lower
margin products, including our Fluent Fluid Management systems, Bolder products (comprised of CoolSeal vessel sealing
devices and JustRight surgical staplers) and Acessa ProVu systems in the current fiscal year.
Operating expenses decreased in fiscal 2022 compared to fiscal 2021 primarily due to a gain of $39.5 million related to
the fair value adjustments to the contingent consideration liability related to the Acessa acquisitions compared to a gain of $6.7
million in the prior year. There was also a decrease in research and development project spend, marketing initiatives, legal
expenses and bad debt, and lower bonus and expense from our deferred compensation plan partially offset by the inclusion of
operating expenses from Bolder of $12.5 million, an increase in commissions from higher sales, an increase in allocated
marketing and charitable contributions, and an increase in travel expenses.
Skeletal Health
September 24, 2022
September 25, 2021
Change
Amount
Amount
Amount
%
Years Ended
Total Revenues
Operating Loss
Operating Loss as a % of Segment Revenue
$
$
$
$
93.6
(7.3)
(7.8) %
$
$
96.9
(2.9)
(3.0) %
(3.3)
(4.4)
(3.4) %
151.7 %
Skeletal Health revenues decreased in fiscal 2022 compared to fiscal 2021 primarily due to the decrease in product
revenues discussed above, partially offset by an increase in service revenue.
Operating loss increased in fiscal 2022 compared to fiscal 2021 primarily due to a decrease in gross profit from lower
revenues and an increase in product cost. Gross margin decreased to 28.2% in the current year compared to 31.4% in the prior
year primarily due to increased costs for our Horizon DXA systems workstation upgrades and lower sales volume of our
Horizon DXA and Insight FD systems primarily due to supply chain constraints, partially offset by a slight increase in average
selling prices of our Horizon DXA and Insight FD systems.
Operating expenses were consistent in fiscal 2022 compared to fiscal 2021.
Fiscal Year Ended September 25, 2021 Compared to Fiscal Year Ended September 26, 2020
Discussions of year-to-year comparisons between fiscal 2021 and 2020 that are not included in this Form 10-K can be
found in “Management’s Discussion and Analysis of Financial Condition and Results of Operations” in Part II, Item 7 of the
Company’s Annual Report on Form 10-K for the fiscal year ended September 25, 2021.
LIQUIDITY AND CAPITAL RESOURCES
At September 24, 2022, we had working capital of $2,924.3 million, and our cash and cash equivalents totaled $2,339.5
million. Our cash and cash equivalents balance increased by $1,169.2 million during fiscal 2022 principally due to cash
generated from operating activities partially offset by cash used in financing and investing activities related to a business
acquisition, repurchases of our common stock and the pay-off of amounts outstanding under the accounts receivable
securitization program (the "Securitization Program").
In fiscal 2022, our operating activities provided cash of $2,125.7 million, primarily due to net income of $1,302.0 million,
non-cash charges for depreciation and amortization aggregating $430.1 million, stock-based compensation expense of $66.7
million and acquired intangible asset impairment charges of $45.1 million. These adjustments to net income were partially
45
Table of Contents
offset by a decrease in net deferred taxes of $166.2 million primarily due to recording a deferred tax asset in connection with an
internal restructuring and intangible asset impairments, and a $39.5 million non-cash adjustment to decrease the contingent
consideration liability to the former shareholder of Acessa. Cash provided by operations included a net cash inflow of $454.2
million from changes in our operating assets and liabilities. The net cash inflow was primarily driven by a $384.3 million dollar
decrease in prepaid expenses and other assets primarily due to tax refunds received in the second quarter related to federal and
state loss carryback claims partially offset by a payment for our Women's Tennis Association sponsorship, and a decrease in
accounts receivable of $272.3 million due to strong collections in the current year and lower revenues in fiscal 2022 compared
to fiscal 2021. These cash inflows were partially offset by an increase in inventory of $136.6 million primarily due to a strategic
buildup of emergency sourced components for our Breast Health business to hedge against the continuing worldwide supply
constraints, a $15.8 million decrease in accrued expenses and other liabilities related to a decrease in accrued compensation and
benefits and payments of value-add taxes partially offset by accrued federal and state income taxes due to timing of payments, a
$23.3 million increase in prepaid income taxes, and a $14.4 million decrease in accounts payable due to the timing of payments.
In fiscal 2022, our investing activities used cash of $206.3 million primarily due to net cash paid for our acquisitions
(primarily Bolder) of $158.6 million and capital expenditures of $127.2 million, which consisted of the purchases of property
and equipment of $70.6 million and $56.6 million for the placement of equipment under customer usage agreements. These
uses of cash in investing activities were partially offset by $75.0 million of proceeds received from the Department of Defense
under a grant to increase production capacity of our two SARS-CoV-2 assays.
In fiscal 2022, our financing activities used cash of $756.0 million, primarily due to $542.1 million for repurchases of our
common stock, $248.5 million for the repayment under the Securitization Program, $63.7 million for the repayment of debt
acquired in the Mobidiag acquisition, $22.9 million for the payment of employee taxes withheld for the net share settlement of
vested stock units, and a $12.2 million contingent consideration payment as a result of the completion of the first annual earn-
out period related to the Acessa acquisition. Partially offsetting these uses of cash were net proceeds of $103.7 million from the
refinancing of the 2021 Credit Agreement and $33.5 million from our equity plans, primarily from the exercise of stock options.
Debt
We had total recorded debt outstanding of $2.82 billion at September 24, 2022, which was comprised of our term loan
under our 2021 Credit Agreement of $1.49 billion (principal of $1.50 billion), 2029 Senior Notes of $936.6 million (principal of
$950.0 million), and 2028 Senior Notes of $396.1 million (principal of $400.0 million).
2021 Credit Agreement
On September 27, 2021, we refinanced our existing term loan and revolving credit facility with Bank of America, N.A. in
its capacity as Administrative Agent, Swing Line Lender and L/C Issuer, and certain other lenders from time to time party
thereto (the "2018 Credit Agreement") by entering into Refinancing Amendment No. 2 dated as of September 27, 2021, to the
Amended and Restated Credit and Guaranty Agreement, dated as of October 3, 2017, as amended (the "2021 Credit
Agreement"). Borrowings under the 2021 Credit Agreement are secured by first-priority liens on, and a first priority security
interest in, substantially all of our U.S. assets and the assets of the Subsidiary Guarantors. These liens are subject to release
during the term of the facilities if we are able to achieve certain corporate or corporate family ratings and other conditions are
met. The credit facilities under the 2021 Credit Agreement (the "2021 Credit Facilities") consist of:
•
•
A $1.5 billion secured term loan ("2021 Term Loan") with a stated maturity date of September 25, 2026; and
A secured revolving credit facility (the "2021 Revolver") under which the Borrowers may borrow up to $2.0 billion,
subject to certain sublimits, with a stated maturity date of September 25, 2026.
As of the date of this Annual Report, there have been no borrowings under the 2021 Revolver.
On August 22, 2022, the Company and its subsidiaries amended the 2021 Credit Agreement by entering into an
amendment (the "Third Amendment") related to the planned phase out of LIBOR by the UK Financial Conduct Authority. The
interest rate applicable to the loans under the 2021 Credit Agreement, after giving effect to the Third Amendment, denominated
in U.S. Dollars were converted to a variant of the secured overnight financing rate (“SOFR”), as established from time to time
by the Federal Reserve Bank of New York, plus a corresponding spread. The Third Amendment converted the Eurocurrency
Rate to Term SOFR plus the SOFR Adjustment of 0.10% and the LIBOR Daily Floating Rate to Daily SOFR Rate plus the
SOFR Adjustment of 0.10%, effective September 23, 2022.
Borrowings under the 2021 Credit Agreement, other than Swing Line Loans, bear interest, at our option, at the Base Rate,
at the Term SOFR Rate, at the Alternative Currency Daily Rate, or at the Daily SOFR Rate, in each case plus the Applicable
Rate.
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Table of Contents
The Applicable Rate in regards to the Base Rate, the Term SOFR Rate, the Alternative Currency Daily Rate, the
Alternative Currency Term Rate and the Daily SOFR Rate is subject to change depending on the Total Net Leverage Ratio (as
defined in the 2021 Credit Agreement). The borrowings of the Term Loan under the 2021 Credit Facilities, after giving effect to
the Third Amendment, initially bear interest at an annual rate equal to the Term SOFR Rate plus the SOFR Adjustment of
0.10% for a one month interest period plus an Applicable Rate equal to 1.00%. As of September 24, 2022, the interest rate
under the 2021 Term Loan was 4.18% per annum.
We are also required to pay a quarterly commitment fee calculated on a daily basis equal to the Applicable Rate as of such
day multiplied by the undrawn committed amount available under the Revolver. As of September 24, 2022, this commitment
fee was 0.15% per annum for the 2021 Revolver.
We are required to make scheduled principal payments under the 2021 Term Loan in increasing amounts ranging from
$3.75 million per three-month period commencing with the three-month period ending on December 29, 2022 to $18.75 million
per three-month period commencing with the three month period ending on December 26, 2025. The remaining scheduled
balance of $1.335 billion (or such lesser aggregate principal amount of the Term Loans then outstanding) on the 2021 Term
Loan and any amounts outstanding under the 2021 Revolver are due at maturity. In addition, subject to the terms and conditions
set forth in the 2021 Credit Agreement, we may be required to make certain mandatory prepayments from the net proceeds of
specified types of asset sales (subject to certain reinvestment rights), debt issuances (excluding permitted debt) and insurance
recoveries (subject to certain reinvestment rights). Certain of the mandatory prepayments are subject to reduction or elimination
if certain financial covenants are met. These mandatory prepayments are required to be applied first to the 2021 Term Loan,
second to any outstanding amount under any Swing Line Loans, third to the 2021 Revolver, fourth to prepay any outstanding
reimbursement obligations with respect to letters of credit and fifth to cash collateralize any letters of credit. Subject to certain
limitations, we may voluntarily prepay any of the 2021 Credit Facilities without premium or penalty. As of September 24,
2022, the outstanding principal balance of the 2021 Term Loan was $1.5 billion, and there were no amounts outstanding under
the 2021 Revolver.
The 2021 Credit Agreement contains affirmative and negative covenants customarily applicable to senior secured credit
facilities, including covenants restricting our ability subject to negotiated exceptions, to incur additional indebtedness and grant
additional liens on our assets, engage in mergers or acquisitions or dispose of assets, enter into sale-leaseback transactions, pay
dividends or make other distributions, voluntarily prepay other indebtedness, enter into transactions with affiliated persons,
make investments, and change the nature of our business. In addition, the 2021 Credit Agreement requires the Borrowers to
maintain certain financial ratios. The 2021 Credit Agreement also contains customary representations and warranties and events
of default, including payments defaults, breach of representations and warranties, covenant defaults, cross defaults and an event
of default upon a change of control of the company.
The 2021 Credit Agreement contains two financial covenants (a total net leverage ratio and an interest coverage ratio)
measured as of the last day of each quarter for the previous twelve month period. As of September 24, 2022, we were in
compliance with these covenants.
2028 Senior Notes
The total aggregate principal balance of the 2028 Senior Notes is $400.0 million. The 2028 Senior Notes are general
senior unsecured obligations and are guaranteed on a senior unsecured basis by certain of our domestic subsidiaries. The 2028
Senior Notes mature on February 1, 2028 and bear interest at the rate of 4.625% per year, payable semi-annually on February 1
and August 1 of each year. We may redeem the 2028 Senior Notes at any time prior to February 1, 2023 at a price equal
to 100% of the aggregate principal amount so redeemed, plus accrued and unpaid interest, if any, to the redemption date and a
make-whole premium set forth in the indenture. We also have the option to redeem the 2028 Senior Notes on or after: February
1, 2023 through February 1, 2024 at 102.312% of par; February 1, 2024 through February 1, 2025 at 101.541% of par; February
1, 2025 through February 1, 2026 at 100.770% of par; and February 1, 2026 and thereafter at 100% of par. In addition, if there
is a change of control coupled with a decline in ratings, as provided in the indenture, we will be required to make an offer to
purchase each holder’s 2028 Senior Notes at a price equal to 101% of their principal amount, plus accrued and unpaid interest,
if any, to the repurchase date.
2029 Senior Notes
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The total aggregate principal balance of the 2029 Senior Notes is $950.0 million. The 2029 Senior Notes are general
senior unsecured obligations and are guaranteed on a senior unsecured basis by certain domestic subsidiaries. The 2029 Senior
Notes mature on February 15, 2029 and bear interest at the rate of 3.250% per year, payable semi-annually on February 15 and
August 15 of each year. We may redeem the 2029 Senior Notes at any time prior to September 28, 2023 at a price equal to
100% of the aggregate principal amount so redeemed, plus accrued and unpaid interest, if any, to the redemption date and a
make-whole premium set forth in the indenture. We may also redeem up to 40% of the aggregate principal amount of the 2029
Senior Notes with the net cash proceeds of certain equity offerings at any time and from time to time before September 28,
2023, at a redemption price equal to 103.250% of the aggregate principal amount so redeemed, plus accrued and unpaid
interest, if any, to the redemption date. We have the option to redeem the 2029 Senior Notes on or after: September 28, 2023
through September 27, 2024 at 101.625% of par; September 28, 2024 through September 27, 2025 at 100.813% of par; and
September 28, 2025 and thereafter at 100% of par. In addition, if there is a change of control coupled with a decline in ratings,
as provided in the indenture, we will be required to make an offer to purchase each holder’s 2029 Senior Notes at a price equal
to 101% of their principal amount, plus accrued and unpaid interest, if any, to the repurchase date.
Accounts Receivable Securitization Program
On June 11, 2021, we amended and restated the Credit and Security agreement to restart the Securitization Program (the
"Securitization Program") and increased the maximum borrowing amount to $320.0 million. Under the terms of the
Securitization Program, we and certain of our wholly-owned subsidiaries sell our customer receivables to a bankruptcy remote
special purpose entity, which is wholly-owned by us. The amount that the special purpose entity may borrow at a given point in
time is determined based on the amount of qualifying receivables that are present in the special purpose entity at such point in
time. The assets of the special purpose entity secure the amounts borrowed and cannot be used to pay our other debts or
liabilities. The Securitization Program provides for annual renewals.
During fiscal 2022, we repaid the outstanding balance of $248.5 million under the Securitization Program. On June 10,
2022, we amended the Credit and Security agreement and temporarily suspended the ability to borrow and the need to comply
with covenants for up to a year. As of September 24, 2022, we did not have any borrowings under this program.
Contingent Consideration Earn-Out Payments
In connection with certain of our acquisitions, we have incurred the obligation to make contingent earn-out payments tied
to performance criteria, principally revenue growth of the acquired business over a specified period. In addition, contractual
provisions relating to these contingent earn-out obligations may result in the risk of litigation relating to the calculation of the
amount due or our operation of the acquired business. Such litigation could be expensive and divert management attention and
resources. Our obligation to make contingent payments may also result in significant operating expenses.
Contingent consideration arrangements are recorded as either additional purchase price or compensation expense if
continuing employment is required to receive such payments. Pursuant to ASC 805, Business Combinations, contingent
consideration that is deemed to be part of the purchase price is recorded as a liability based on the estimated fair value of the
consideration we expect to pay to the former shareholders of the acquired business as of the acquisition date. This liability is re-
measured each reporting period with the change in fair value recorded through a separate line item within our Consolidated
Statements of Income. Increases or decreases in the fair value of contingent consideration liabilities can result from changes in
discount rates, changes in the timing, probabilities and amount of revenue estimates, and accretion of the liability for the
passage of time.
Currently, our only contingent consideration liability is from our Acessa acquisition. We have an obligation to the
former Acessa shareholders to make contingent payments based on a multiple of annual incremental revenue growth over a
three year period ending annually in December. There is no maximum earnout. Pursuant to ASC 805, the contingent
consideration was deemed to be part of the purchase price, and we recorded our estimate of the fair value of the contingent
consideration liability utilizing the Monte Carlo simulation based on future revenue projections of the business, comparable
companies revenue growth rates, implied volatility and applying a risk adjusted discount rate. The first earn-out period was
completed in December 2021, and we paid $12.2 million to the former shareholders in the second quarter of fiscal 2022. As of
September 24, 2022 this liability was recorded at its fair value of $23.4 million.
Stock Repurchase Program
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On December 9, 2020, our Board of Directors authorized a new five-year share repurchase program, to repurchase up to
$1.0 billion of our outstanding common stock. During fiscal 2022, we repurchased 7.7 million shares of our common stock for a
total consideration of $542.1 million. On September 22, 2022, our Board of Directors authorized a new stock repurchase
program, with a five-year term, to repurchase up to $1.0 billion of our outstanding common stock, effective as of the close of
trading on September 23, 2022. This new stock repurchase authorization replaced the previous $1.0 billion authorization, which
had $149.7 million remaining as of September 22, 2022. Subsequent to September 24, 2022, we repurchased 1.5 million shares
of our common stock for total consideration of $100.0 million. The timing of any future share repurchases will be based upon
our continuing analysis of market, financial, and other factors. Repurchases under the authorized share repurchase program may
be made using a variety of methods, which may include, but are not limited to, open market purchases, privately negotiated
transactions, accelerated share repurchase agreements, or purchases pursuant to a Rule 10b5-1 plan under the Exchange Act.
The authorized share repurchase program may be suspended, delayed or discontinued at any time.
Future Liquidity Considerations
We expect to continue to review and evaluate potential strategic transactions that we believe will complement our current
or future business. Subject to the "Risk Factors" set forth in Part I, Item 1A of this Annual Report and the general disclaimers
set forth in our Special Note Regarding Forward-Looking Statements at the outset of this Annual Report, we believe that our
cash and cash equivalents, cash flows from operations, the cash available under our 2021 Revolver will provide us with
sufficient funds in order to fund our expected normal operations and debt payments over the next twelve months. Our longer-
term liquidity is contingent upon future operating performance. We may also require additional capital in the future to fund
capital expenditures, repayment of debt, acquisitions, strategic transactions or other investments. As described above, we have
significant indebtedness outstanding under our 2021 Credit Agreement, 2028 Senior Notes, and 2029 Senior Notes. These
capital requirements could be substantial. Our operating performance may also be affected by matters discussed under the
above-referenced Risk Factors set forth elsewhere in this report. These risks, trends and uncertainties may also adversely affect
our long-term liquidity.
Legal Contingencies
We are currently involved in certain legal proceedings and claims. In connection with these legal proceedings and claims,
management periodically reviews estimates of potential costs to be incurred by us in connection with the adjudication or
settlement, if any, of these proceedings. These estimates are developed, as applicable in consultation with outside counsel, and
are based on an analysis of potential litigation outcomes and settlement strategies. In accordance with ASC 450, Contingencies,
loss contingencies are accrued if, in the opinion of management, an adverse outcome is probable and such financial outcome
can be reasonably estimated. It is possible that future results for any particular quarter or annual period may be materially
affected by changes in our assumptions or the effectiveness of our strategies relating to these proceedings.
Guarantees and Other Off-Balance Sheet Arrangements
We do not have guarantees or other off-balance sheet financing arrangements, including variable interest entities, of a
magnitude that we believe could have a material impact on our financial condition or liquidity.
CRITICAL ACCOUNTING POLICIES AND ESTIMATES
The discussion and analysis of our financial condition and results of operations are based upon our consolidated financial
statements, which have been prepared in accordance with U.S. generally accepted accounting principles. The preparation of
these consolidated financial statements requires us to make estimates and judgments that affect the reported amounts of assets,
liabilities, revenues and expenses, and related disclosure of contingent assets and liabilities. On an on-going basis, we evaluate
our estimates, including those related to revenue recognition for multiple element arrangements, allowance for doubtful
accounts, reserves for excess and obsolete inventories, valuations, purchase price allocations and contingent consideration
related to business combinations, expected future cash flows including growth rates, discount rates, terminal values and other
assumptions used to evaluate the recoverability of long-lived assets and goodwill, estimated fair values of intangible assets and
goodwill, amortization methods and periods, warranty reserves, certain accrued expenses, restructuring and other related
charges, stock-based compensation, contingent liabilities, tax reserves and recoverability of our net deferred tax assets and
related valuation allowances. We base our estimates on historical experience and various other assumptions that are believed to
be reasonable under the circumstances. Actual results could differ from these estimates if past experience or other assumptions
do not turn out to be substantially accurate. Any differences may have a material impact on our financial condition and results
of operations.
The following is a discussion of what we believe to be the more significant critical accounting policies and estimates used
in the preparation of our consolidated financial statements.
Inventory
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Our inventories include material, labor and overhead, and are stated at the lower of cost (first-in, first-out) or market. As a
developer and manufacturer of high technology medical equipment and diagnostic test kits, we may be exposed to a number of
economic and industry factors that could result in portions of our inventory becoming either obsolete or in excess of anticipated
usage. Our policy is to establish inventory reserves when conditions exist that suggest that our inventory may be in excess of
anticipated demand or is obsolete based upon our assumptions about future demand for our products and market conditions.
Although considerable effort is made to ensure the accuracy of our forecasts of future product demand, any significant
unanticipated changes in demand or expected usage could have a significant negative impact on the value of our inventory and
our operating results.
Business Combinations
We record tangible and intangible assets acquired and liabilities assumed in business combinations under the purchase
method of accounting. Amounts paid for each acquisition are allocated to the assets acquired and liabilities assumed based on
their fair values at the dates of acquisition. Contingent consideration, which is not deemed to be linked to continuing
employment, is recorded at fair value measured on the date of acquisition using an appropriate valuation model, such as the
Monte Carlo simulation model. The value recorded is based on estimates of future financial projections under various potential
scenarios, in which the model runs many simulations based on comparable companies' growth rates and their implied volatility.
These cash flow projections are discounted with a risk adjusted rate. Each quarter until such contingent amounts are earned, the
fair value of the liability is remeasured at each reporting period and adjusted as a component of operating expenses based on
changes to the underlying assumptions. The estimates used to determine the fair value of the contingent consideration liability
are subject to significant judgment, specifically projected revenues, and given the inherent uncertainties in making these
estimates, actual results are likely to differ from the amounts originally recorded and could be materially different.
The fair value of identifiable intangible assets is based on detailed valuations that use information and assumptions
provided by management, which consider management’s best estimate of inputs and assumptions that a market participant
would use. We allocate any excess purchase price over the fair value of the net tangible and intangible assets acquired and
liabilities assumed to goodwill.
We generally use the income approach in which cash flow projections on an after-tax basis are discounted using a risk
adjusted rate to determine the estimated fair value of certain identifiable intangible assets including developed technology, in-
process research and development projects, customer relationships, and trade names. The significant assumptions used to
estimate the fair value of intangible assets include discount rates and certain assumptions that form the basis of the forecasted
results specifically revenue growth rates. These significant assumptions are forward looking and could be affected by future
economic and market conditions.
With respect to property, plant and equipment, we estimate the fair value of these assets using a combination of the cost
and market approaches, depending on the component. Generally, we apply the cost or income approach as the primary methods
in estimating the fair value of land and buildings as the market approach is less reliable based on potential significant
differences between the property being valued and the potentially comparable sales of similar properties.
Goodwill
We test goodwill at the reporting unit level for impairment on an annual basis and between annual tests if events and
circumstances indicate it is more likely than not that the fair value of a reporting unit is less than its carrying value. Events that
could indicate impairment and trigger an interim impairment assessment include, but are not limited to current economic and
market conditions, including a decline in market capitalization, a significant adverse change in legal factors, business climate,
operational performance of the business or key personnel, and an adverse action or assessment by a regulator. Our annual
impairment test date is the first day of our fiscal fourth quarter.
In performing the test, we either use the qualitative assessment permitted by ASC 350, Intangibles—Goodwill and Other,
or the single step quantitative approach prescribed under ASC 350 including amendments under ASU 2017-04. Under the
qualitative approach we consider a number of factors, including the amount by which the previous quantitative test's fair value
exceeded the carrying value of the reporting units, the forecasts in our then-current strategic plan compared to the forecasts in
the previous quantitative test, an evaluation of discount rates, long-term growth rates including the terminal year rate, if tax
rates would have significantly changed, an evaluation of current economic factors for both the worldwide economy and
specifically the medical device industry, and any significant changes in customer and supplier relationships. We weigh these
factors to determine if it is more likely than not that the fair value of the reporting unit exceeds its carrying value. If after
performing a qualitative assessment, indicators are present, or we identify factors that cause us to believe it is appropriate to
perform a more precise calculation of fair value, we would move beyond the qualitative assessment and perform a quantitative
impairment test.
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Under the quantitative impairment test, we perform a comparison of the reporting unit’s carrying value to its fair value.
We consider a number of factors to determine the fair value of a reporting unit, including an independent valuation to conduct
this test. The valuation is based upon expected future discounted operating cash flows of the reporting unit as well as analysis of
recent sales and ratio comparisons of similar companies. We base the discount rate on the weighted average cost of capital, or
WACC, of market participants. If the carrying value of a reporting unit exceeds its estimated fair value, we apply the single step
approach under ASU 2017-04. As a result of this simplified approach the goodwill impairment is calculated as the amount by
which the carrying value of the reporting unit exceeds its fair value to the extent of the goodwill balance.
We conducted our fiscal 2022 annual impairment test on the first day of the fourth quarter and utilized the quantitative
approach. We used discounted cash flows, or DCF, and market approaches to estimate the fair value of our reporting units as of
June 26, 2022 and ultimately used the fair value determined by the DCF in making our impairment test conclusions. We believe
we used reasonable estimates and assumptions about future revenue, cost projections, cash flows, market multiples and discount
rates as of the measurement date. As a result of completing this analysis, all of our reporting units had fair values exceeding
their carrying values.
At September 24, 2022, we believe that our reporting units, with goodwill aggregating $3.2 billion, were not at risk of
failing the goodwill impairment test based on our current forecasts and qualitative assessment.
Since the fair value of our reporting units was determined by use of the DCF, and the key assumptions that drive the fair
value in this model are the WACC, terminal values, growth rates, and the amount and timing of expected future cash flows,
significant judgment is applied in determining fair value. If the current economic environment were to deteriorate, this would
likely result in a higher WACC because market participants would require a higher rate of return. In the DCF as the WACC
increases, the fair value decreases. The other significant factor in the DCF is our projected financial information (i.e., amount
and timing of expected future cash flows and growth rates) and if these assumptions were to be adversely impacted, this could
result in a reduction of the fair value of a reporting unit.
Intangible Assets
Intangible assets are initially recorded at fair value and stated net of accumulated amortization and impairments. We
amortize intangible assets that have finite lives using either the straight-line method, or if reliably determinable, based on the
pattern in which the economic benefit of the asset is expected to be utilized. We evaluate the recoverability of our definite lived
intangible assets whenever events or changes in circumstances or business conditions indicate that the carrying value of these
assets may not be recoverable based on expectations of future undiscounted cash flows for each asset group. If the carrying
value of an asset or asset group exceeds its undiscounted cash flows, we estimate the fair value of the assets, generally utilizing
a discounted cash flow analysis based on the present value of estimated future cash flows to be generated by the assets using a
risk-adjusted discount rate. To estimate the fair value of the assets, the Company uses market participant assumptions pursuant
to ASC 820, Fair Value Measurements.
Indefinite lived intangible assets, such as IPR&D assets, are initially recorded at fair value and are required to be tested
for impairment annually, or more frequently if indicators of impairment are present. The Company’s annual impairment test
date is as of the first day of its fourth quarter. We estimate the fair value of IPR&D assets utilizing a discounted cash flow
analysis and key assumptions are revenue growth rates, timing of completion of the project, costs to complete the project and
discount rates. These estimates require significant judgment and adverse changes in assumptions could result in a lower fair
value.
Revenue Recognition
We generate revenue from the sale of our products, primarily medical imaging systems and diagnostic and surgical
disposable products, and related services, which are primarily support and maintenance services on our medical imaging
systems. See Note 3 for further discussion of revenue recognition.
We consider revenue to be earned when all of the following criteria are met: we have a contract with a customer that
creates enforceable rights and obligations; promised products or services are identified; the transaction price, or the amount that
we expect to receive, including an estimate of uncertain amounts subject to a constraint to ensure revenue is not recognized in
an amount that would result in a significant reversal upon resolution of the uncertainty, is determinable; and we have transferred
control of the promised items to the customer. A performance obligation is a promise in a contract to transfer a distinct good or
service to the customer and is the unit of account in the contract. The transaction price for the contract is measured as the
amount of consideration we expect to receive in exchange for the goods and services expected to be transferred. A contract's
transaction price is allocated to each distinct performance obligation and recognized as revenue when, or as, control of the
distinct good or service is transferred. Transfer of control for our products is generally at shipment or delivery, depending on
contractual terms, but occurs when title and risk of loss transfers to the customer which represents the point in time when the
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customer obtains the use of and substantially all of the remaining benefit of the product. As such, the performance obligation
related to product sales is satisfied at a point in time. Revenue from support and maintenance contracts and extended warranties
are recognized over time based on the contract term, which represents a faithful depiction of the transfer of goods and services
given the stand-ready nature of the performance obligations. Service revenue related to professional services for installation,
training and repairs is recognized as the services are performed based on the specific nature of the service.
We recognize receivables when we have an unconditional right to payment, which represents the amount we expect to
collect in a transaction and is most often equal to the transaction price in the contract. Payment terms are typically 30 days in
the U.S. but may be longer in international markets. We treat shipping and handling costs performed after a customer obtains
control of the good as a fulfillment cost and record these costs within costs of product revenue when the corresponding revenue
is recognized.
Some of our contracts have multiple performance obligations. For contracts with multiple performance obligations, we
are required to allocate the transaction price to each performance obligation using our best estimate of the standalone selling
price of each distinct good or service in the contract. We determine the best estimate of standalone selling price using average
selling prices over 3- to 12-month periods of data depending on the products or nature of the services coupled with current
market considerations. If the product or service does not have a history of sales or if sales volume is not sufficient, we rely on
prices set by our pricing committees or applicable marketing department adjusted for expected discounts.
We exercise judgement in estimating variable consideration, which includes volume discounts, sales rebates, product
returns and other adjustments. These amounts are recorded as a reduction to revenue and classified as a current liability. We
base our estimates for volume discounts and sales rebates on historical information to the extent it is reasonable to be used as a
predictive tool of expected future rebates. To the extent the transaction price includes variable consideration, we apply
judgment in constraining the estimated variable consideration due to factors that may cause reversal of revenue recognized. We
evaluate constraints based on our historical and projected experience with similar customer contracts. Our contracts for the sale
of capital equipment and related components, and assays and tests typically do not provide the right to return product, however,
our contracts for the sale of our interventional breast and surgical handpieces provide for a right of return for a limited period of
time. In general, estimates of variable consideration and constraints are not material to our financial statements.
We also place instruments (or equipment) at customer sites but retain title to the instrument (for example, the ThinPrep
Processor, ThinPrep Imaging System, and the Panther system). The customer has the right to use the instrument for a period of
time, and then we recover the cost of providing the instrument through the sales of disposables, namely tests and assays in
Diagnostics and handpieces in GYN Surgical. These types of agreements include an embedded operating lease for the right to
use an instrument and no instrument revenue is recognized at the time of instrument delivery. We recognize a portion of the
revenue allocated to the embedded lease concurrent with the sale of disposables over the term of the agreement.
Income Taxes
We use the asset and liability method for accounting for income taxes in accordance with ASC 740, Income Taxes. Under
this method, we recognize deferred income tax assets and liabilities for the future tax consequences of differences between the
financial statement carrying amount of existing assets and liabilities and their respective tax bases, and also for operating loss
and tax credit carry-forwards at each reporting period. We measure deferred tax assets and liabilities using enacted tax rates and
laws applicable to the period and jurisdiction in which we expect the differences to affect taxable income. We evaluate both the
positive and negative evidence that affects the realizability of net deferred tax assets and assess the need for a valuation
allowance. The future benefit to be derived from our deferred tax assets is dependent upon our ability to generate sufficient
future taxable income in each jurisdiction of the right type to realize the assets. We establish a valuation allowance when
necessary to reduce deferred tax assets to the amounts expected to be realized. To the extent we establish or release a valuation
allowance, a tax charge or benefit will be recorded as a component of the income tax provision on the statement of operations in
the reporting period that such determination is made.
We have recognized $74.6 million in net deferred tax liabilities at September 24, 2022 and $228.6 million at
September 25, 2021. The decrease was primarily due to recording a deferred tax asset in connection with an internal
restructuring and intangible asset impairments in fiscal 2022. The liabilities primarily relate to deferred taxes associated with
our acquisitions. The tax assets primarily relate to net operating and capital loss carryforwards, accruals and reserves, stock-
based compensation, and research credits.
Accounting for income taxes requires a two-step approach to recognize and measure uncertain tax positions. The first
step is to evaluate the tax position for recognition by determining if, based on the technical merits, it is more likely than not that
the position will be sustained upon audit, including resolutions of related appeals or litigation processes, if any. The second step
is to measure the tax benefit as the largest amount that is more than 50% likely of being realized upon ultimate settlement. We
evaluate these uncertain tax positions on a quarterly basis. This evaluation is based on factors including, but not limited to,
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changes in facts or circumstances, changes in tax law, effectively settled issues under audit and new audit activity. Any change
in these factors could result in the recognition of a tax benefit or an additional charge to the tax provision.
As of September 24, 2022, we had $247.6 million in gross unrecognized tax benefits excluding interest, of which $231.6
million, if recognized, would reduce our effective tax rate. As of September 25, 2021, we had $212.8 million in gross
unrecognized tax benefits excluding interest, of which $197.0 million, if recognized, would have reduced our effective tax rate.
In the ordinary course of business, there are many transactions and calculations where the ultimate tax outcome is
uncertain. Judgment is required in determining our worldwide income tax provision. In our opinion, we have made adequate
provisions for income taxes for all years subject to audit. While we consider our estimates reasonable, no assurance can be
given that the final tax outcome will not be different than amounts reflected in our historical income tax provisions and
accruals. If our assumptions are incorrect, the differences could have a material impact on our income tax provision and
operating results in the period in which such determination is made.
Recent Accounting Pronouncements
See Note 2 to our consolidated financial statements contained in Item 15 of this Annual Report.
Item 7A. Quantitative and Qualitative Disclosures About Market Risk
Financial Instruments, Other Financial Instruments, and Derivative Commodity Instruments. Financial instruments
consist of cash and cash equivalents, accounts receivable, equity investments, foreign currency derivative contracts, an interest
rate swap agreement, insurance contracts, accounts payable and debt obligations. Except for our outstanding 2028 and 2029
Senior Notes, the fair value of these financial instruments approximate their carrying amount. The fair value of our 2028 and
2029 Senior Notes was approximately $365.7 million and $783.9 million, respectively, as of September 24, 2022. Amounts
outstanding under our 2021 Credit Agreement of $1.5 billion aggregate principal as of September 24, 2022 are subject to
variable rates of interest based on current market rates, and as such, we believe the carrying amount of these obligations
approximates fair value.
Primary Market Risk Exposures. Our primary market risk exposure is in the areas of interest rate risk and foreign
currency exchange rate risk. We incur interest expense on borrowings outstanding under our 2028 and 2029 Senior Notes, and
2021 Credit Agreement. The 2028 and 2029 Senior Notes have fixed interest rates. Effective September 25, 2022 (the first day
of fiscal 2023), borrowings under our 2021 Credit Agreement bear interest at the SOFR Rate plus SOFR Adjustment of 0.10%
plus the applicable margin of 1.00% per annum.
As of September 24, 2022, there was $1.5 billion of aggregate principal outstanding under the 2021 Credit Agreement.
Since this debt obligation is a variable rate instrument, our interest expense associated with this debt instrument is subject to
change. A hypothetical 10% adverse movement (increase in the SOFR rate) would increase annual interest expense by
approximately $1.6 million, which is net of the impact of our interest rate swap hedge. We previously entered into an interest
rate swap agreement to help mitigate the interest rate volatility associated with the variable rate interest on the amounts
outstanding under our credit facilities. The critical terms of the interest rate swap were designed to mirror the terms of our
SOFR-based borrowings under the 2021 Credit Agreement, and therefore the interest rate swap is highly effective at offsetting
the cash flows being hedged. We designated this derivative instrument as a cash flow hedge of the variability of the Term
SOFR-based interest payments on $1.0 billion of principal. The interest rate swap contract expires on December 17, 2023.
The return from cash and cash equivalents will vary as short-term interest rates change. A hypothetical 10% increase or
decrease in interest rates, however, would not have a material adverse effect on our financial condition.
Foreign Currency Exchange Risk. Our international business is subject to risks, including, but not limited to: unique
economic conditions, changes in political climate, differing tax structures, other regulations and restrictions, and foreign
exchange rate volatility. Accordingly, our future results could be materially adversely impacted by changes in these or other
factors.
We conduct business worldwide and maintain sales and service offices outside the U.S. as well as manufacturing
facilities in Costa Rica and the United Kingdom. Our international sales are denominated in a number of currencies, primarily
the Euro, U.S. dollar, UK Pound and Chinese Renminbi. The majority of our foreign subsidiaries functional currency is the
local currency, although certain foreign subsidiaries functional currency is the U.S. dollar based on the nature of their
operations or functions. Fluctuations in the foreign currency rates could affect our sales, cost of goods and operating margins
and could result in exchange losses. In addition, currency devaluations can result in a loss if we hold deposits of that currency.
We have executed forward foreign currency contracts to hedge a portion of results denominated in the Euro, UK Pound,
Australian dollar, Japanese Yen, Canadian dollar and Chinese Renminbi. These contracts do not qualify for hedge accounting.
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As a result, we may experience volatility in our Consolidated Statements of Income due to (i) the impact of unrealized gains
and losses reported in other income, net on the mark-to-market of outstanding contracts and (ii) realized gains and losses
recognized in other income, net, whereas the offsetting economic gains and losses are reported in the line item of the underlying
cash flow, for example, revenue.
We believe that the operating expenses of our international subsidiaries that are incurred in local currencies will not have
a material adverse effect on our business, results of operations or financial condition. Our operating results and certain assets
and liabilities that are denominated in foreign currencies are affected by changes in the relative strength of the U.S. dollar
against those currencies. Our expenses, denominated in foreign currencies, are positively affected when the U.S. dollar
strengthens against those currencies and adversely affected when the U.S. dollar weakens. However, we believe that the foreign
currency exchange risk is not significant. We believe a hypothetical 10% increase or decrease in foreign currencies that we
transact in would not have a material adverse impact on our financial condition or results of operations. During fiscal 2022, we
incurred net foreign exchange gains of $48.5 million, net foreign exchange losses of $15.1 million in fiscal 2021 and net foreign
exchange gains of $3.4 million in fiscal 2020.
Item 8. Financial Statements and Supplementary Data
Our Consolidated Financial Statements and Supplementary Data are set forth under Part IV, Item 15, which is
incorporated herein by reference.
Item 9. Changes in and Disagreements with Accountants on Accounting and Financial Disclosure
None.
Item 9A. Controls and Procedures
Evaluation of Disclosure Controls and Procedures
We maintain disclosure controls and procedures that are designed to ensure that information required to be disclosed in
our Exchange Act reports is recorded, processed, summarized and reported within the time periods specified in the SEC’s rules
and forms, and that such information is accumulated and communicated to our management, including our Chief Executive
Officer and Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosure. In designing and
evaluating the disclosure controls and procedures, management recognized that any controls and procedures, no matter how
well designed and operated, can provide only reasonable assurance of achieving the desired control objectives, as ours are
designed to do, and management necessarily was required to apply its judgment in evaluating the cost-benefit relationship of
possible controls and procedures.
As of September 24, 2022, we carried out an evaluation, under the supervision and with the participation of our
management, including our Chief Executive Officer and Chief Financial Officer, of the effectiveness of the design and
operation of our disclosure controls and procedures, as defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act.
Based upon that evaluation, our Chief Executive Officer and Chief Financial Officer concluded that our disclosure controls and
procedures are effective.
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Report of Management on Internal Control over Financial Reporting
We are responsible for establishing and maintaining adequate internal control over financial reporting. Internal control
over financial reporting is defined in Rule 13a-15(f) and 15d-15(f) under the Exchange Act, as amended, as a process designed
by, or under the supervision of our principal executive and principal financial officers and effected by our board of directors,
management and other personnel to provide reasonable assurance regarding the reliability of financial reporting and the
preparation of financial statements for external purposes in accordance with U.S. generally accepted accounting principles and
includes those policies and procedures that:
•
•
•
pertain to the maintenance of records that in reasonable detail accurately and fairly reflect the transactions and
disposition of our assets;
provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in
accordance with generally accepted accounting principles, and that our receipts and expenditures are being made only in
accordance with authorization of our management and directors; and
provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use or disposition of
our assets that could have a material effect on the financial statements.
Our internal control system was designed to provide reasonable assurance to our management and board of directors
regarding the preparation and fair presentation of published financial statements. 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 risks 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 assessed the effectiveness of our internal control over financial reporting as of September 24, 2022. In
making this assessment, we used the criteria set forth by the Committee of Sponsoring Organizations of the Treadway
Commission (2013 framework) (COSO) in Internal Control-Integrated Framework.
Management has excluded from our assessment of and conclusion on the effectiveness of internal control over financial
reporting the internal controls of Bolder Surgical Holdings, Inc., which is included in the consolidated financial statements of
Hologic, Inc. as of and for the year ended September 24, 2022 and constituted $168.2 million and $142.4 million of our total
assets and net assets, respectively, as of September 24, 2022 and $9.9 million and $18.0 million of revenues and pre-tax losses,
respectively, for the year then ended.
Subject to the foregoing, based on management’s assessment, we believe that, as of September 24, 2022, our internal
control over financial reporting is effective at a reasonable assurance level based on these criteria.
Ernst & Young LLP, an independent registered public accounting firm, has issued an attestation report on the
effectiveness of our internal control over financial reporting. This report in which they expressed an unqualified opinion is
included below.
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Report of Independent Registered Public Accounting Firm
To the Board of Directors and Stockholders of Hologic, Inc.
Opinion on Internal Control over Financial Reporting
We have audited Hologic, Inc.’s internal control over financial reporting as of September 24, 2022, based on criteria
established in Internal Control—Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway
Commission (2013 framework) (the COSO criteria). In our opinion, Hologic, Inc. (the Company) maintained, in all material
respects, effective internal control over financial reporting as of September 24, 2022, based on the COSO criteria.
As indicated in the accompanying Report of Management on Internal Control over Financial Reporting, management’s
assessment of and conclusion on the effectiveness of internal control over financial reporting did not include the internal
controls of Bolder Surgical Holdings, Inc., which is included in the 2022 consolidated financial statements of the Company and
constituted $168.2 million and $142.4 million of total and net assets, respectively, as of September 24, 2022 and $9.9 million
and $18.0 million of revenues and pre-tax losses, respectively, for the year then ended. Our audit of internal control over
financial reporting of the Company also did not include an evaluation of the internal control over financial reporting of Bolder
Surgical Holdings, Inc.
We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United
States) (PCAOB), the 2022 consolidated financial statements of the Company and our report dated November 15, 2022
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 Report of
Management 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 the U.S. federal securities laws and the applicable
rules and regulations of the Securities and Exchange Commission and the PCAOB.
We conducted our audit 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, testing and evaluating the design and operating effectiveness of internal control based on the assessed
risk, and performing such other procedures as we considered necessary in the circumstances. We believe that our audit provides
a reasonable basis for our opinion.
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 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.
56
Table of Contents
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/ Ernst & Young LLP
Boston, Massachusetts
November 15, 2022
57
Table of Contents
Changes in Internal Control over Financial Reporting
During the quarter ended September 24, 2022, there have been no changes in our internal control over financial reporting
that have materially affected, or are reasonably likely to materially affect, our internal control over financial reporting.
Item 9B. Other Information
None.
58
Table of Contents
PART III
Item 10. Directors, Executive Officers and Corporate Governance
Pursuant to Section 406 of the Sarbanes-Oxley Act of 2002, we have adopted a Code of Ethics for Senior Financial
Officers that applies to our principal executive officer, principal financial officer, and principal accounting officer and
controller, and other persons performing similar functions. Our Code of Ethics for Senior Financial Officers is publicly
available on our website at investors.hologic.com as Appendix A to our Code of Conduct. We intend to satisfy the disclosure
requirement under Item 5.05 of Current Report on Form 8-K regarding an amendment to, or waiver from, a provision of this
code by posting such information on our website, at the address specified above.
The additional information required by this item is incorporated by reference to our Definitive Proxy Statement for our
annual meeting of stockholders to be filed with the SEC within 120 days after the close of our fiscal year.
Item 11. Executive Compensation
The information required by this item is incorporated by reference to our Definitive Proxy Statement for our annual
meeting of stockholders to be filed with the SEC within 120 days after the close of our fiscal year.
Item 12. Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters
We maintain a number of equity compensation plans for employees, officers, directors and others whose efforts
contribute to our success. The table below sets forth certain information as of the end of our fiscal year ended September 24,
2022 regarding the shares of our common stock available for grant or granted under stock option plans and equity incentives
that (i) were approved by our stockholders, and (ii) were not approved by our stockholders.
Equity Compensation Plan Information
Plan Category
Equity compensation plans approved by security
holders (1)
Equity compensation plans not approved by security
holders
Total
___________
Number of
securities to be
issued upon
exercise of
outstanding
options, warrants
and rights
(a)
Weighted-average
exercise price of
outstanding
options,
warrants and rights
(b) (2)
Number of securities
remaining available for
future issuance under
equity compensation
plans (excluding
securities reflected in
column (a))
(c)
7,255,678 $
— $
7,255,678 $
48.46
—
48.46
3,345,813
—
3,345,813
(1) Includes 2,920,969 shares that are issuable upon restricted stock units (RSUs), performance stock units (PSUs) and market
stock units (MSUs) vesting. The remaining balance consists of outstanding stock option grants.
(2) The weighted average exercise price does not take into account the shares issuable upon vesting of outstanding RSUs,
PSUs and MSUs, which have no exercise price.
The additional information required by this item is incorporated by reference to our Definitive Proxy Statement for our
annual meeting of stockholders to be filed with the SEC within 120 days after the close of our fiscal year.
Item 13. Certain Relationships and Related Transactions and Director Independence
The information required by this item is incorporated by reference to our Definitive Proxy Statement for our annual
meeting of stockholders to be filed with the SEC within 120 days after the close of our fiscal year.
Item 14. Principal Accounting Fees and Services
The information required by this item is incorporated by reference to our Definitive Proxy Statement for our annual
meeting of stockholders to be filed with the SEC within 120 days after the close of our fiscal year. Our independent public
accounting firm is Ernst & Young LLP, New York, NY, PCAOB Auditor ID [PCAOB ID: 42].
59
Table of Contents
PART IV
Item 15. Exhibits and Financial Statement Schedules
(a) The following documents are filed as part of this report:
(1) Financial Statements
Report of Independent Registered Public Accounting Firm on Consolidated Financial Statements
Consolidated Statements of Income for the years ended September 24, 2022, September 25, 2021 and
September 26, 2020
Consolidated Statements of Comprehensive Income for the years ended September 24, 2022, September 25,
2021 and September 26, 2020
Consolidated Balance Sheets as of September 24, 2022 and September 25, 2021
Consolidated Statements of Stockholders’ Equity for the years ended September 24, 2022, September 25,
2021 and September 26, 2020
Consolidated Statements of Cash Flows for the years ended September 24, 2022, September 25, 2021 and
September 26, 2020
Notes to Consolidated Financial Statements
(2) Financial Statement Schedules
All schedules have been omitted because they are not required or because the required information is given
in the Consolidated Financial Statements or Notes thereto.
(b) Listing of Exhibits
Exhibit
Number
Exhibit Description
2.1 Asset Purchase Agreement, dated December 14, 2016, by and among Hologic,
Inc., Grifols Diagnostic Solutions Inc. and Grifols, S.A.
Securities Purchase Agreement, dated as of November 20, 2019, by and among
Hologic, Inc., Hologic Holdings Limited and Lotus Buyer, Inc. (6)
2.2
2.3 Share Purchase Agreement, dated as of April 8, 2021, by and among Hologic,
Inc. and certain sellers listed therein (6)
3.1
Certificate of Incorporation of Hologic, with amendments
3.2
4.1
Seventh Amended and Restated Bylaws of Hologic, Inc.
Specimen Certificate for Shares of Hologic’s Common Stock (filed in paper
format)
4.2
Indenture, dated September 28, 2020, by and among Hologic, Inc., the
guarantors party thereto and Wells Fargo Bank, National Association, as Trustee
4.3 First Supplemental Indenture dated as of May 18, 2021 among Hologic, Inc.,
The Subsidiary Guarantor Party Hereto and Wells Fargo Bank, National
Association, as Trustee
4.4 Form of 3.250% Senior Note due 2029 (included in Exhibit 4.2)
4.5
Indenture dated January 19, 2018, by and among Hologic, the Guarantors party
thereto and Wells Fargo Bank, National Association, as Trustee
60
Incorporated by
Reference
Form
8-K
8-K
8-K
Filing Date/
Period End
Date
12/15/2016
11/20/2019
04/08/2021
10-K
09/30/2017
8-K
8-A
8-K
06/25/2019
01/31/1990
09/28/2020
10-K
09/25/2021
8-K
8-K
09/28/2020
01/19/2018
Exhibit
Number
Exhibit Description
4.6 First Supplemental Indenture dated January 19, 2018, by and among Hologic,
the Guarantors party thereto and Wells Fargo Bank, National Association, as
Trustee
4.7 Form of 4.625% Senior Note due 2028 (included in Exhibit 4.5)
4.8 Second Supplemental Indenture dated as of November 9, 2018 among Hologic,
Inc., The Subsidiary Guarantor Parties Hereto and Wells Fargo Bank, National
Association, as Trustee
4.9 Third Supplemental Indenture dated as of January 8, 2019 among Hologic, Inc.,
the Subsidiary Guarantors Party Hereto and Wells Fargo Bank, National
Association, as Trustee
4.10 Fourth Supplemental Indenture dated as of March 14, 2019 among Hologic, Inc.,
The Subsidiary Guarantor Party Hereto and Wells Fargo Bank, National
Association, as Trustee
4.11 Fifth Supplemental Indenture dated as of May 18, 2021 among Hologic, Inc., the
Subsidiary Guarantor Party Hereto and Wells Fargo Bank, National Association,
as Trustee
4.12 Description of Securities
10.1* Hologic Amended and Restated 2008 Equity Incentive Plan.
10.2* Form of Stock Option Award Agreement Under 2008 Equity Incentive Plan
(adopted fiscal 2016).
10.3* Form of Stock Option Award Agreement Under 2008 Equity Incentive Plan
(adopted fiscal 2017).
Incorporated by
Reference
Form
8-K
8-K
10-K
Filing Date/
Period End
Date
01/19/2018
01/19/2018
09/25/2021
10-K
09/25/2021
10-K
09/25/2021
10-K
09/25/2021
10-K
09/28/2019
8-K
8-K
8-K
03/15/2018
10/14/2015
11/09/2016
10.4* Form of Stock Option Award Agreement Under 2008 Equity Incentive Plan
(Outside US) (adopted fiscal 2017)
Filed
Herewith
10.5* Form of Restricted Stock Unit Award Agreement Under 2008 Equity Incentive
8-K
11/09/2016
Plan (adopted fiscal 2017).
10.6* Form of Restricted Stok Unit Award Agreement Under 2008 Equity Incentive
Plan (Outside US) (adopted fiscal 2017)
Filed
Herewith
10.7* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (relative TSR) (adopted fiscal 2020).
10.8* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (ROIC) (adopted fiscal 2020).
10.9* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (Free Cash Flow) (adopted fiscal 2020).
10.10* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (relative TSR) (adopted fiscal 2021).
10.11* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (ROIC) (adopted fiscal 2021).
10.12* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (Free Cash Flow) (adopted fiscal 2021).
10.13* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (ROIC – Outside US) (adopted fiscal 2021).
10.14* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (relative TSR – Outside US) (adopted fiscal 2021).
61
8-K
8-K
8-K
8-K
8-K
8-K
8-K
8-K
11/08/2019
11/08/2019
11/08/2019
11/06/2020
11/06/2020
11/06/2020
11/06/2020
11/06/2020
Exhibit
Number
Exhibit Description
10.15* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (Free Cash Flow – Outside US) (adopted fiscal 2021).
10.16* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (relative TSR) (adopted fiscal 2022).
10.17* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (ROIC) (adopted fiscal 2022).
10.18* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (Free Cash Flow) (adopted fiscal 2022).
10.19* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (ROIC – Outside US) (adopted fiscal 2022).
10.20* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (relative TSR – Outside US) (adopted fiscal 2022).
10.21* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (Free Cash Flow – Outside US) (adopted fiscal 2022).
10.22* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (relative TSR) (adopted fiscal 2023).
10.23* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (ROIC) (adopted fiscal 2023).
10.24* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (Free Cash Flow) (adopted fiscal 2023).
10.25* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (ROIC – Outside US) (adopted fiscal 2023).
10.26* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (relative TSR – Outside US) (adopted fiscal 2023).
10.27* Form of Performance Stock Unit Award Agreement Under 2008 Equity
Incentive Plan (Free Cash Flow – Outside US) (adopted fiscal 2023).
Incorporated by
Reference
Form
8-K
8-K
8-K
8-K
8-K
8-K
8-K
8-K
8-K
8-K
8-K
8-K
8-K
Filing Date/
Period End
Date
11/06/2020
11/04/2021
11/04/2021
11/04/2021
11/04/2021
11/04/2021
11/04/2021
11/04/2022
11/04/2022
11/04/2022
11/04/2022
11/04/2022
11/04/2022
10.28* Form of Independent Director Restricted Stock Unit Award Agreement Under
10-K
09/28/2013
2008 Equity Incentive Plan (annual grant).
10.29* Hologic, Inc. 2012 Employee Stock Purchase Plan, as amended
10.30* Hologic Short-Term Incentive Plan, as amended and restated
10.31* Hologic Amended and Restated Deferred Equity Plan
10.32*
Rabbi Trust Agreement.
10.33* Form of Indemnification Agreement (as executed with each director of Hologic).
10.34*
Employment Agreement dated December 6, 2013 by and between Stephen P.
MacMillan and Hologic.
10.35*
Amended and Restated Employment Agreement by and between the Company
and Stephen P. MacMillan, dated September 18, 2015.
8-K
8-K
8-K
03/04/2016
11/07/2018
12/16/2015
10-K
09/28/2013
8-K
8-K
8-K
03/06/2009
12/09/2013
09/21/2015
10.36* Amendment No. 1 to Amended and Restated Employment Agreement by and
between the Company and Stephen P. MacMillan, dated September 24, 2016.
10-K
09/24/2016
10.37* Amendment No. 2 to Amended and Restated Employment Agreement by and
8-K
10/06/2020
between the Company and Stephen P. MacMillan, dated October 5, 2020.
10.38* Form of Matching Restricted Stock Unit Award Agreement
8-K
12/09/2013
62
Exhibit
Number
Exhibit Description
10.39* Change of Control Agreement dated December 6, 2013 by and between Stephen
P. MacMillan and Hologic.
Incorporated by
Reference
Form
8-K
Filing Date/
Period End
Date
12/09/2013
10.40* Severance and Change of Control Agreement dated July 31, 2018 by and
8-K
07/31/2018
between Karleen M. Oberton and Hologic, Inc.
10.41* Severance and Change of Control Agreement dated February 2, 2015 by and
10-Q
03/28/2015
between John M. Griffin and Hologic.
10.42* Severance and Change of Control Agreement dated September 15, 2020 by and
8-K
09/15/2020
between Kevin R. Thornal and Hologic, Inc.
10.43* Amended Contract of Employment between Jan Verstreken and Hologic dated
10-Q
12/26/2020
December 11, 2020
10.44* Severance and Change of Control Agreement dated June 28, 2021 by and
10-Q
06/26/2021
between Elisabeth (Lisa) Hellmann and Hologic, Inc.
10.45* Transition Agreement by and between Sean S. Daugherty and Hologic, Inc.
dated October 1, 2022
10.46* Form of Division President Severance Agreement (1)
10.47* Form of Senior Vice President Severance Agreement (2)
10.48* Form of Change of Control Agreement (3)
Filed
Herewith
Filed
Herewith
Filed
Herewith
Filed
Herewith
10.49
Office Lease dated December 31, 2003 between Cytyc and Marlborough
Campus Limited Partnership.
10.50 First Amendment to that Office Lease dated December 31, 2003 between Cytyc
and Marlborough Campus Limited Partnership, entered into August 23, 2017, by
and between Hines Global REIT Marlborough Campus LLC and Hologic, Inc.
(4)
Cytyc
Corporation
10-K
12/31/2003
10-K
09/30/2017
10.51
Lease Agreement by and between Zona Franca Coyol S.A. and Cytyc Surgical
Products Costa Rica S.A. dated April 23, 2007.
10-K
09/29/2007
10.52 Addendum 1 to Lease Agreement by and between Zona Franca Coyol S.A. and
10-K
09/28/2019
Cytyc Surgical Products Costa Rica S.A. dated July 22, 2007. (5) (6)
10.53 Addendum 2 to Lease Agreement by and between Zona Franca Coyol S.A. and
10-K
09/28/2019
Cytyc Surgical Products Costa Rica S.A. dated September 22, 2008. (5) (6)
10.54 Addendum No. 3 to Current Lease by and Between BCR Fondo de Inversion
10-Q
12/30/2017
Inmobiliario and Hologic Surgical Products Costa Rica S.R.L. (4)
10.55
Lease Agreement by and between 445 Simarano Drive, Marlborough LLC and
Cytyc dated July 11, 2006.
10-K
09/29/2007
10.56
First Amendment to Lease by and between 445 Simarano Drive Marlborough
LLC and Hologic, Inc. dated July 14, 2016. (5)
10-K
09/28/2019
10.57 Lease of land situate at Crewe Road, Wythenshawe in the City of Manchester
10-K
09/25/2021
between the Council of the City of Manchester and V.G. Instruments Group
Limited dated February 8, 1988 (5)
63
Exhibit
Number
10.58
10.59
Exhibit Description
Amended and Restated Credit and Guaranty Agreement, originally dated May
29, 2015, and amended and restated as of October 3, 2017 among Hologic,
Hologic GGO 4 Ltd, each Designated Borrower from time to time party thereto,
the Guarantors from time to time party thereto, each Lender from time to time
party thereto and Bank of America, N.A., as Administrative Agent, Swing Line
Lender and L/C Issuer.
Incorporated by
Reference
Form
8-K
Filing Date/
Period End
Date
10/04/2017
Refinancing Amendment No. 1 dated as of December 17, 2018 to the Amended
and Restated Credit and Guaranty Agreement dated as of October 3, 2017.
8-K
12/18/2018
10.60 Refinancing Amendment No. 2, dated as of September 27, 2021, to the
8-K
09/27/2021
Amended and Restated Credit and Guaranty Agreement dated as of October 3,
2017, as amended.
10.61 Refinancing Amendment No. 3, dated as of August 22, 2022, to the Amended
and Restated Credit and Guaranty Agreement dated as of October 3, 2017, as
amended.
Filed
Herewith
10.62
Supply Agreement for Panther Instrument System effective November 22, 2006
between Gen-Probe Incorporated and STRATEC Biomedical Systems AG. (4)
Gen-Probe
10-Q
09/30/2007
10.63 Amendment No. 1 dated June 1, 2011 to Supply Agreement for Panther
10-K
09/24/2016
Instrument System. (4)
10.64 Amendment No. 2 dated February 28, 2013 to Supply Agreement for Panther
10-K
09/24/2016
Instrument System. (4)
10.65
Intellectual Property License, dated as of January 31, 2017, by and among
Hologic, Inc., Gen-Probe Incorporated and Grifols Diagnostics Solutions Inc.
8-K
02/02/2017
10.66 First Amendment, dated as of April 9, 2019, to Intellectual Property License,
dated as of January 31, 2017, by and among Hologic, Inc., Gen-Probe
Incorporated and Grifols Diagnostic Solutions.
10-Q
03/30/2019
21.1
Subsidiaries of Hologic.
23.1
Consent of Independent Registered Public Accounting Firm.
31.1
Certification of Hologic’s CEO pursuant to Item 601(b)(31) of Regulation S-K,
as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
Filed
herewith
Filed
herewith
Filed
herewith
31.2
Certification of Hologic’s CFO pursuant to Item 601(b)(31) of Regulation S-K,
as adopted pursuant to Section 302 of the Sarbanes-Oxley Act of 2002.
Filed
herewith
32.1
Certification of Hologic’s CEO pursuant to 18 U.S.C. Section 1350, as adopted
pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
32.2
Certification of Hologic’s CFO pursuant to 18 U.S.C. Section 1350, as adopted
pursuant to Section 906 of the Sarbanes-Oxley Act of 2002.
101.INS
Inline XBRL Instance Document - the instance document does not appear in the
Interactive Data File because its XBRL tags are embedded within the Inline
XBRL document.
101.SCH
101.CAL
Inline XBRL Taxonomy Extension Schema Document.
Inline XBRL Taxonomy Extension Calculation Linkbase Document.
Furnished
herewith
Furnished
herewith
Filed
herewith
Filed
herewith
Filed
herewith
64
Incorporated by
Reference
Exhibit
Number
101.DEF
101.LAB
101.PRE
Inline XBRL Taxonomy Extension Definition Linkbase Document.
Exhibit Description
Inline XBRL Taxonomy Extension Label Linkbase Document.
Inline XBRL Taxonomy Extension Presentation Linkbase Document.
104 Cover Page Interactive Data File (formatted as inline XBRL and contained in
Exhibit 101)
Form
Filed
herewith
Filed
herewith
Filed
herewith
Filed
herewith
Filing Date/
Period End
Date
Indicates management contract or compensatory plan, contract or arrangement.
______________
*
(1) The registrant has entered into this agreement with the following executive officers: Essex D. Mitchell.
(2) The registrant has entered into this agreement with the following executive officers: Erik S. Anderson.
(3) The registrant has entered into this agreement with the following executive officers: Essex D. Mitchell and Erik S.
Anderson.
(4)
Confidential treatment has been granted with respect to certain portions of this exhibit. A complete version of this
exhibit has been filed separately with the SEC.
Certain portions of this exhibit are considered confidential and have been omitted as permitted under SEC rules and
regulations.
Schedules and exhibits have been omitted pursuant to Item 601(b)(2) of Regulation S-K.
(5)
(6)
65
Item 16. Form 10-K Summary
None.
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
HOLOGIC, INC.
By:
/S/ STEPHEN P. MACMILLAN
Stephen P. MacMillan
Chairman, President and Chief Executive Officer
Date: November 15, 2022
Pursuant to the requirements of the Securities Exchange Act of 1934, this report has been signed below by the
following persons on behalf of the registrant and in the capacities and on the dates indicated.
Signature
Title
Date
/S/ STEPHEN P. MACMILLAN
STEPHEN P. MACMILLAN
/S/ KARLEEN M. OBERTON
KARLEEN M. OBERTON
/S/ BENJAMIN J. COHN
BENJAMIN J. COHN
/S/ SALLY W. CRAWFORD
SALLY W. CRAWFORD
/S/ CHARLES DOCKENDORFF
CHARLES DOCKENDORFF
/S/ SCOTT T. GARRETT
SCOTT T. GARRETT
/S/ LUDWIG N. HANTSON
LUDWIG N. HANTSON
/S/ NAMAL NAWANA
NAMAL NAWANA
/S/ CHRISTIANA STAMOULIS
CHRISTIANA STAMOULIS
/S/ AMY M. WENDELL
AMY M. WENDELL
Chairman, President and Chief
Executive Officer (Principal Executive
Officer)
November 15, 2022
Chief Financial Officer (Principal
Financial Officer)
November 15, 2022
Vice President, Corporate Controller
(Principal Accounting Officer)
November 15, 2022
Lead Independent Director
November 15, 2022
November 15, 2022
November 15, 2022
November 15, 2022
November 15, 2022
November 15, 2022
November 15, 2022
Director
Director
Director
Director
Director
Director
66
Table of Contents
Hologic, Inc.
Consolidated Financial Statements
Years ended September 24, 2022, September 25, 2021 and September 26, 2020
Contents
Report of Independent Registered Public Accounting Firm
Consolidated Financial Statements
Consolidated Statements of Income
Consolidated Statements of Comprehensive Income
Consolidated Balance Sheets
Consolidated Statements of Stockholders’ Equity
Consolidated Statements of Cash Flows
Notes to Consolidated Financial Statements
F-2
F-5
F-6
F-7
F-8
F-10
F-12
F-1
Table of Contents
Report of Independent Registered Public Accounting Firm
To the Board of Directors and Stockholders of Hologic, Inc.
Opinion on the Financial Statements
We have audited the accompanying consolidated balance sheets of Hologic, Inc. (the Company) as of September 24,
2022 and September 25, 2021, the related consolidated statements of income, comprehensive income, stockholders’ equity and
cash flows for each of the three years in the period ended September 24, 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 September 24, 2022 and September 25, 2021, and the results of its operations
and its cash flows for each of the three years in the period ended September 24, 2022, in conformity with U.S. generally
accepted accounting principles.
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 September 24, 2022, based on criteria
established in Internal Control—Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway
Commission (2013 framework) and our report dated November 15, 2022 expressed an unqualified opinion thereon.
Basis for Opinion
These financial statements are the responsibility of the Company’s management. Our responsibility is to express an
opinion on the Company’s 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 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
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 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 financial statements. We believe that our audits provide a reasonable basis for our opinion.
Critical Audit Matters
The critical audit matters communicated below are matters arising from the current period audit of the financial
statements that were communicated or required to be communicated to the audit committee and that: (1) relate to accounts or
disclosures that are material to the financial statements and (2) involved our especially challenging, subjective or complex
judgments. The communication of critical audit matters 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 matters below, providing separate opinions on
the critical audit matters or on the accounts or disclosures to which they relate.
Description of
the Matter
Product Revenue Recognition
As discussed in Note 3 to the consolidated financial statements, the Company generates product revenue
from the sale of medical imaging systems and diagnostic and surgical disposable products. The
Company’s contracts for capital equipment sales generally have multiple performance obligations.
Auditing the timing and amount of revenue recognized for product sales required significant auditor
judgment because it involves several subjective management assumptions and estimates including the
identification of performance obligations within the contracts, the estimation of the standalone selling
price of each performance obligation, the determination of the transaction price and the allocation of the
transaction price to each performance obligation, and a determination of the point in time at which those
performance obligations were satisfied.
F-2
Table of Contents
How We
Addressed the
Matter in Our
Audit
We obtained an understanding, evaluated the design and tested the operating effectiveness of controls
over the Company’s processes to account for product revenue recognition, including management’s
controls over determining the transaction price, the identification of performance obligations in revenue
contracts, the estimation of the standalone selling price for each performance obligation, the allocation of
the transaction price to each performance obligation, and the determination of the point in time at which
the Company transferred control of the promised items to the customer.
To test product revenue, we evaluated whether management’s revenue recognition policies are appropriate
and in accordance with ASC 606 Revenue from Contracts with Customers. We tested management’s
determination of the transaction price by comparing the price to the customer contract for a sample of
transactions. We tested management’s identification of the performance obligations and the allocation of
transaction price to each performance obligation by performing an independent assessment, in comparison
to the standard, on a sample of customer contracts. We tested management’s estimated standalone selling
prices for its identified performance obligations based on actual prices charged for similar products and
services sold on a standalone basis. We also tested management’s assertion that control was transferred
to the customer by inspecting documentation supporting the transfer of control for a sample of contracts.
In addition, we performed other procedures which included, among others, analytical procedures over
product revenue and testing a sample of revenue transactions that occurred near the end of the fiscal year
to evaluate accounting cut-off. We also compared the Company’s revenue recognition disclosures
included in Note 3 to the consolidated financial statements to disclosures required by the relevant
accounting guidance.
Description of
the Matter
Business Combination
As described in Note 5 to the consolidated financial statements, during 2022, the Company completed one
business combination for total consideration of $160.1 million. The business combination resulted in the
recognition of intangible assets of $96.7 million.
Auditing the Company’s accounting for the business combination was complex due to the significant
estimation required by management to determine the fair value of identified intangible assets, which
principally consisted of developed technology related to currently marketed products, totaling $73.6
million. The Company used an income approach to measure the fair value of the acquired developed
technology intangible assets. The significant assumptions used to estimate the fair value of these
intangible assets included discount rates and certain assumptions that form the basis of the forecasted
results, specifically revenue growth rates. These significant assumptions are forward looking and could be
affected by future economic and market conditions.
F-3
Table of Contents
How We
Addressed the
Matter in Our
Audit
We obtained an understanding, evaluated the design and tested the operating effectiveness of the controls
over the Company’s accounting for the business combination. For example, we tested controls over the
identification and valuation of intangible assets, including the valuation models and underlying
assumptions used to develop such estimates.
To test the estimated fair value of the developed technology, we performed audit procedures that included,
among others, evaluating the Company's use of the selected valuation model for each estimate and testing
the significant assumptions described above that were used in the models. We tested the completeness and
accuracy of the underlying data used in each analysis. For example, to evaluate revenue growth rates, we
compared the assumptions used to current industry, market and economic trends, to the historical results
of the acquired business, and to other guideline companies within the same industry. We also performed
sensitivity analyses over the significant assumptions used to evaluate the changes in the fair value of each
estimate that would result from changes in the assumptions. We involved our valuation professionals to
test the models and the significant assumptions noted above. We also compared the Company’s
disclosures included in Note 5 to the consolidated financial statements to disclosures required by the
relevant accounting guidance.
/s/ Ernst & Young LLP
We have served as the Company’s auditor since 2002.
Boston, Massachusetts
November 15, 2022
F-4
Table of Contents
Consolidated Statements of Income
(In millions, except number of shares, which are reflected in thousands, and per share data)
Hologic, Inc.
Revenues:
Product
Service and other
Costs of revenues:
Product
Amortization of acquired intangible assets
Impairment of acquired intangible assets and
equipment
Service and other
Gross Profit
Operating expenses:
Research and development
Selling and marketing
General and administrative
Amortization of acquired intangible assets
Impairment of acquired intangible assets and
equipment
Contingent consideration – fair value adjustments
Restructuring and divestiture charges
Income from operations
Interest income
Interest expense
Debt extinguishment loss
Other income (expense), net
Income before income taxes
Provision (benefit) for income taxes
Net income
Net loss attributable to noncontrolling interest
Net income attributable to Hologic
Net income per common share attributable to Hologic:
Basic
Diluted
Weighted average number of shares outstanding:
Basic
Diluted
September 24,
2022
Years ended
September 25,
2021
September 26,
2020
$
4,191.2 $
4,967.3 $
3,227.0
671.6
4,862.8
1,166.1
295.7
17.4
386.2
2,997.4
283.4
630.3
407.7
45.2
27.7
(39.5)
2.4
1,357.2
1,640.2
12.9
(95.1)
(0.7)
30.9
1,588.2
286.2
1,302.0 $
—
1,302.0 $
665.0
5,632.3
1,205.1
276.7
—
354.7
3,795.8
276.3
561.2
433.2
42.2
—
(6.7)
9.3
1,315.5
2,480.3
1.4
(93.6)
(21.6)
(5.4)
2,361.1
491.4
1,869.7 $
(1.8)
1,871.5 $
549.4
3,776.4
953.7
253.2
25.8
316.2
2,227.5
222.5
484.6
355.7
39.7
4.4
0.3
15.3
1,122.5
1,105.0
4.3
(116.5)
—
9.1
1,001.9
(108.6)
1,110.5
(4.7)
1,115.2
5.18 $
5.13 $
7.28 $
7.21 $
4.24
4.21
251,527
253,845
257,046
259,706
262,727
264,613
$
$
$
$
See accompanying notes.
F-5
Table of Contents
Net income
Hologic, Inc.
Consolidated Statements of Comprehensive Income
(In millions)
September 24,
2022
Years ended
September 25,
2021
September 26,
2020
$
1,302.0 $
1,869.7 $
1,110.5
Changes in foreign currency translation adjustment
(224.1)
(20.2)
Changes in pension plans, net of taxes of $0.4 in 2022,
$0.2 in 2021, and $0.1 in 2020.
Gain (loss) recognized, net of tax of $13.7 in 2022, $2.5 in
2021, and $(8.3) in 2020 for interest rate swaps
Changes in value of hedged interest rate caps, net of tax of
$0.2 in 2021, and $0.5 in 2020
Gain (loss) recognized in other comprehensive loss
Loss reclassified from accumulated other
comprehensive loss to the statement of operations,
net
Other comprehensive loss
Comprehensive income
Components of comprehensive income attributable to
noncontrolling interest:
Net loss attributable to noncontrolling interest
Comprehensive loss attributable to noncontrolling interest
1.0
44.0
—
—
0.5
9.4
0.4
0.5
18.5
(0.1)
(27.6)
(0.5)
2.3
(179.1)
(9.4)
(7.4)
$
1,122.9 $
1,860.3 $
1,103.1
—
—
1.8
1.8
4.7
4.7
Comprehensive income attributable to Hologic
$
1,122.9 $
1,862.1 $
1,107.8
See accompanying notes.
F-6
Table of Contents
Consolidated Balance Sheets
(In millions, except number of shares, which are reflected in thousands, and par value)
Hologic, Inc.
September 24,
2022
September 25,
2021
ASSETS
Current assets:
Cash and cash equivalents
Accounts receivable
Inventory
Prepaid expenses and other current assets
Prepaid income taxes
Total current assets
Property, plant and equipment, net
Intangible assets, net
Goodwill
Other assets
Total assets
LIABILITIES AND STOCKHOLDERS’ EQUITY
Current liabilities:
Current portion of long-term debt
Accounts payable
Accrued expenses
Deferred revenue
Finance lease obligations
Total current liabilities
Long-term debt, net of current portion
Finance lease obligations, net of current portion
Deferred income tax liabilities
Deferred revenue, net of current portion
Other long-term liabilities
Commitments and contingencies (Note 13 and 14)
Stockholders’ equity:
Preferred stock, $0.01 par value – 1,623 shares authorized; 0 shares issued
Common stock, $0.01 par value – 750,000 shares authorized; 298,533 and
297,306 shares issued, respectively
Additional paid-in-capital
Retained earnings
Treasury stock, at cost – 51,401 and 43,653 shares, respectively
Accumulated other comprehensive loss
Total stockholders’ equity
Total liabilities and stockholders’ equity
See accompanying notes.
$
$
$
$
2,339.5 $
617.6
623.7
232.2
49.0
3,862.0
481.6
1,280.6
3,236.5
210.5
9,071.2 $
15.0 $
197.7
535.3
186.5
3.2
937.7
2,808.4
18.0
90.8
9.4
330.7
1,170.3
942.7
501.2
528.8
25.7
3,168.7
564.7
1,659.2
3,281.6
245.7
8,919.9
313.0
215.9
596.2
198.0
3.7
1,326.8
2,712.2
22.8
250.5
20.3
368.7
—
—
3.0
6,042.6
1,600.3
(2,531.5)
(238.2)
4,876.2
9,071.2 $
3.0
5,965.8
298.3
(1,989.4)
(59.1)
4,218.6
8,919.9
F-7
Table of Contents
Balance at September 28,
2019
Noncontrolling interest
created in acquisition
Accounting standard
transition adjustment - ASC
842
Exercise of stock options
Vesting of restricted stock
units, net of shares withheld
for employee taxes
Common stock issued
under the employee stock
purchase plan
Stock-based compensation
expense
Net income (loss)
Foreign currency
translation adjustment
Adjustment to minimum
pension liability, net
Repurchase of common
stock
Accelerated share
repurchase agreement
Unrealized loss on interest
rate cap
Unrealized loss on interest
rate swap
Interest cost of interest rate
cap reclassified to income
Purchase of non-controlling
interest
Balance at September 26,
2020
Exercise of stock options
Vesting of restricted stock
units, net of shares withheld
for employee taxes
Common stock issued
under the employee stock
purchase plan
Stock-based compensation
expense
Net income (loss)
Foreign currency
translation adjustment
Adjustment to minimum
pension liability, net
Repurchase of common
stock
Unrealized gain on interest
rate cap
Unrealized gain on interest
rate swap
Interest cost of interest rate
cap reclassified to income
Purchase of non-controlling
interest
Balance at September 25,
2021
Hologic, Inc.
Consolidated Statements of Stockholders' Equity
(In millions, except number of shares, which are reflected in thousands)
Common Stock
Number of
Shares
Par
Value
Additional
Paid-in-
Capital
Retained
Earnings
(Accumulated
Deficit)
Accumulated
Other
Comprehensive
Loss
Treasury Stock
Number of
Shares
Amount
Noncontrolling
Interest
Total
Stockholders’
Equity
292,323 $ 2.9 $ 5,769.8 $
(2,688.7) $
(42.3)
24,638 $
(926.0) $
— $
2,115.7
—
—
—
—
—
1,761
—
—
48.3
611
—
(14.2)
412
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
17.6
83.3
—
—
—
—
—
—
—
—
—
0.3
—
—
—
1,115.2
—
—
—
—
—
—
—
— $ — $
— $
— $
—
—
—
—
—
—
—
18.5
(0.1)
—
—
(0.5)
(27.6)
2.3
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
9,064
(448.6)
3,907
(205.0)
—
—
—
— $
—
—
—
—
8.6
—
—
—
—
—
(4.7)
—
—
—
—
—
—
—
(1.8)
8.6
0.3
48.3
(14.2)
17.6
83.3
1,110.5
18.5
(0.1)
(448.6)
(205.0)
(0.5)
(27.6)
2.3
(1.8)
295,107 $ 2.9 $ 5,904.8 $
(1,573.2) $
(49.7)
37,609 $ (1,579.6) $
2.1 $
2,707.3
857
—
32.9
980
0.1
(47.6)
362
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
18.9
65.0
—
—
—
—
—
—
—
—
—
(8.2)
—
—
—
—
1,871.5
—
—
—
—
—
—
—
—
—
—
—
—
(20.2)
0.5
—
0.4
9.4
0.5
—
—
—
—
—
—
—
—
—
—
—
—
—
—
—
6,044
(409.8)
—
—
—
—
—
—
—
—
—
—
—
—
(1.8)
—
—
—
—
—
—
32.9
(47.5)
18.9
65.0
1,869.7
(20.2)
0.5
(409.8)
0.4
9.4
0.5
(0.3)
(8.5)
297,306 $ 3.0 $ 5,965.8 $
298.3 $
(59.1)
43,653 $ (1,989.4) $
— $
4,218.6
F-8
Table of Contents
Exercise of stock options
Vesting of restricted stock
units, net of shares withheld
for employee taxes
Common stock issued
under the employee stock
purchase plan
Stock-based compensation
expense
Net income
Foreign currency
translation adjustment
Adjustment to minimum
pension liability, net
Repurchase of common
stock
Unrealized gain on interest
rate swap
Balance at September 24,
2022
336
—
13.8
561
—
(22.9)
330
—
—
—
—
—
—
—
—
—
—
—
—
—
19.2
66.7
—
—
—
—
—
—
—
—
—
1,302.0
—
—
—
—
—
—
—
—
—
(224.1)
1.0
—
44.0
—
—
—
—
—
—
—
—
—
—
—
—
—
—
7,748
(542.1)
—
—
—
—
—
—
—
—
—
—
—
13.8
(22.9)
19.2
66.7
1,302.0
(224.1)
1.0
(542.1)
44.0
298,533 $ 3.0 $ 6,042.6 $
1,600.3 $
(238.2)
51,401 $ (2,531.5) $
— $
4,876.2
See accompanying notes.
F-9
Table of Contents
Hologic, Inc.
Consolidated Statements of Cash Flows
(In millions)
Years ended
September 24,
2022
September 25,
2021
September 26,
2020
$
1,302.0 $
1,869.7
$
1,110.5
83.1
292.9
83.3
(94.4)
30.2
0.3
—
27.0
(427.1)
(25.3)
(3.8)
(286.2)
(4.9)
96.0
15.0
896.6
(119.4)
139.3
(98.3)
—
(58.1)
—
(5.1)
OPERATING ACTIVITIES
Net income
Adjustments to reconcile net income to net cash provided by operating activities:
Depreciation
Amortization
Stock-based compensation expense
Deferred income taxes and other non-cash taxes
Intangible asset and equipment impairment charges
Contingent consideration fair value adjustments
Debt extinguishment loss
Other adjustments and non-cash items
Changes in operating assets and liabilities, excluding the effect of
acquisitions and dispositions:
Accounts receivable
Inventory
Prepaid income taxes
Prepaid expenses and other assets
Accounts payable
Accrued expenses and other liabilities
Deferred revenue
89.2
340.9
66.7
(166.2)
45.1
(39.5)
0.7
32.6
272.3
(136.6)
(23.3)
384.3
(14.4)
(15.8)
(12.3)
88.0
318.9
65.0
(70.1)
—
(6.7)
21.6
31.0
110.9
(84.1)
13.0
(56.3)
20.4
(4.9)
14.0
Net cash provided by operating activities
2,125.7
2,330.4
INVESTING ACTIVITIES
Acquisition of businesses, net of cash acquired
(158.6)
(1,164.7)
Net proceeds from sale of business
Purchase of property and equipment
Proceeds from the Department of Defense
Increase in equipment under customer usage agreements
Purchase of intellectual property
Other activity
—
(70.6)
75.0
(56.6)
—
4.5
—
(118.3)
21.5
(59.4)
(6.5)
(2.2)
Net cash used in investing activities
(206.3)
(1,329.6)
(141.6)
FINANCING ACTIVITIES
Proceeds from long-term debt, net of issuance costs
Repayment of long-term debt
Proceeds from senior notes, net of issuance costs
Repayment of senior notes
Proceeds from revolving credit line
Repayments under revolving credit line
Proceeds from accounts receivable securitization agreement
Repayments under accounts receivable securitization agreement
Repayment of acquired long-term debt
Purchase of non-controlling interest
Payment of contingent consideration
Payment of deferred acquisition consideration
Repurchases of common stock
F-10
1,491.2
(1,387.5)
—
—
—
—
—
(248.5)
(63.7)
—
(12.2)
—
—
(75.0)
936.3
(970.8)
—
(250.0)
320.0
(71.5)
—
(8.5)
—
(1.9)
(542.1)
(409.8)
—
(45.8)
—
—
750.0
(500.0)
16.0
(250.0)
—
(1.8)
—
(24.3)
(653.6)
Table of Contents
Net proceeds from issuance of common stock under employee stock plans
33.5
51.3
65.6
Payment of minimum tax withholdings on net share settlements of equity
awards
Payments under finance lease obligations
Net cash used in financing activities
Effect of exchange rate changes on cash and cash equivalents
Net increase in cash and cash equivalents
Cash and cash equivalents, beginning of period
Cash and cash equivalents, end of period
(22.9)
(3.8)
(756.0)
5.8
1,169.2
1,170.3
(47.5)
(2.4)
(529.8)
(1.7)
469.3
701.0
$
2,339.5 $
1,170.3
$
(14.3)
(1.7)
(659.9)
4.1
99.2
601.8
701.0
See accompanying notes.
F-11
Table of Contents
Notes to Consolidated Financial Statements
(all tabular amounts in millions, except number of shares which are reflected in thousands)
Hologic, Inc.
1. Operations
Hologic, Inc. (the “Company” or “Hologic”) develops, manufactures and supplies premium diagnostics products, medical
imaging systems, and surgical products with an emphasis on women's health and well-being through early detection and
treatment. Until December 30, 2019, the Company's product portfolio included light-based aesthetic and medical treatment
systems sold by its former Medical Aesthetics business. The Company completed the sale of its Medical Aesthetics segment on
December 30, 2019 (the first day of the second quarter of fiscal 2020).
2. Summary of Significant Accounting Policies
Principles of Consolidation
The consolidated financial statements include the accounts of the Company and its wholly owned subsidiaries. All
intercompany transactions and balances have been eliminated in consolidation. The Company’s fiscal year ends on the last
Saturday in September. Fiscal 2022, 2021 and 2020 ended on September 24, 2022, September 25, 2021 and September 26,
2020, respectively. Fiscal 2022, 2021 and 2020 were 52-week years. Fiscal 2023 will be a 53-week year.
Subsequent Events Consideration
The Company considers events or transactions that occur after the balance sheet date but prior to the issuance of the
financial statements to provide additional evidence for certain estimates or to identify matters that may require additional
disclosure. Subsequent events have been evaluated as required. There were no material recognized or unrecognized subsequent
events recorded in the consolidated financial statements as of and for the year ended September 24, 2022.
Management’s Estimates and Uncertainties
The preparation of financial statements in conformity with U.S. generally accepted accounting principles ("GAAP")
requires management to make significant estimates and assumptions that affect the reported amounts of assets and liabilities and
disclosure of contingent assets and liabilities at the date of the financial statements and the reported amounts of revenues and
expenses during the reporting periods. Significant estimates and assumptions by management affect the Company’s revenue
recognition for multiple performance obligation arrangements, valuations, purchase price allocations and contingent
consideration related to business combinations, expected future cash flows including growth rates, discount rates, terminal
values and other assumptions and estimates used to evaluate the recoverability of long-lived assets and goodwill, estimated fair
values of intangible assets and goodwill, amortization methods and periods, accounts receivable reserves, inventory excess and
obsolescence reserves, warranty reserves, certain accrued expenses, restructuring and other related charges, contingent
liabilities, tax reserves, deferred tax rates and recoverability of the Company’s net deferred tax assets and related valuation
allowances, and stock-based compensation.
Although the Company regularly assesses these estimates, actual results could differ materially from these estimates.
Changes in estimates are recorded in the period in which they become known. The Company bases its estimates on historical
experience and various other assumptions that it believes to be reasonable under the circumstances.
The Company is subject to a number of risks similar to those of other companies of similar size in its industry, including
supply chain constraints primarily related to electronic components, primarily semiconductor chips, dependence on third-party
reimbursements to support the markets of the Company’s products, early stage of development of certain products, rapid
technological changes, recoverability of long-lived assets (including intangible assets and goodwill), competition, stability of
world financial markets, ability to obtain regulatory approvals, changes in the regulatory environment, limited number of
suppliers, customer concentration, integration of acquisitions, substantial indebtedness, government regulations, management of
international activities, protection of proprietary rights, patent and other litigation, dependence on contract manufacturers and
dependence on key individuals.
Cash Equivalents
Cash equivalents are highly liquid investments with insignificant interest rate risk and maturities of three months or less
at the time of acquisition.
F-12
Table of Contents
Concentrations of Credit Risk
Financial instruments that subject the Company to credit risk primarily consist of cash and cash equivalents, equity
investments and trade accounts receivable. The Company invests its cash and cash equivalents with high credit quality financial
institutions.
The Company’s customers are principally located in the U.S., Europe and Asia. The Company performs ongoing credit
evaluations of the financial condition of its customers and generally does not require collateral. Although the Company is
directly affected by the overall financial condition of the healthcare industry, as well as global economic conditions,
management does not believe significant credit risk exists as of September 24, 2022. The Company generally has not
experienced any material losses related to receivables from individual customers or groups of customers in the healthcare
industry. The Company maintains an allowance for doubtful accounts based on accounts past due and historical collection
experience.
There were no customers with a balance greater than 10% of accounts receivable as of September 24, 2022 and
September 25, 2021. There were no customers that represented greater than 10% of consolidated revenues for fiscal years 2022,
2021 and 2020.
Concentration of Suppliers
The Company purchases certain components of its products from a single or small number of suppliers. A change in or
loss of these suppliers could cause a delay in filling customer orders and a possible loss of sales, which could adversely affect
results of operations.
Supplemental Cash Flow Statement Information
Years ended
Cash paid during the period for income taxes
Cash paid during the period for interest
Non-Cash Financing Activities:
Fair value of contingent consideration at acquisition
$
$
$
36.2 $
99.7 $
615.1 $
93.2 $
— $
— $
265.9
109.5
82.7
September 24, 2022
September 25, 2021
September 26, 2020
Cash paid for income taxes presented above is net of tax refunds of $430.4 million, $13.7 million and $15.5 million for
fiscal years 2022, 2021 and 2020, respectively, driven primarily by federal and state loss carryback claims.
Inventories
Inventories are valued at the lower of cost or market on a first-in, first-out basis. Work-in-process and finished goods
inventories consist of materials, labor and manufacturing overhead. The valuation of inventory requires management to estimate
excess and obsolete inventory. The Company employs a variety of methodologies to determine the net realizable value of its
inventory. Provisions for excess and obsolete inventory are primarily based on management’s estimates of forecasted sales,
usage levels and expiration dates, as applicable for certain disposable products. A significant change in the timing or level of
demand for the Company’s products compared to forecasted amounts may result in recording additional charges for excess and
obsolete inventory in the future. The Company records charges for excess and obsolete inventory within cost of product
revenues.
Inventories consisted of the following:
Raw materials
Work-in-process
Finished goods
September 24, 2022
September 25, 2021
$
$
252.9 $
60.1
310.7
623.7 $
163.3
53.0
284.9
501.2
F-13
Table of Contents
Property, Plant and Equipment
Property, plant and equipment is recorded at cost less accumulated depreciation and impairments. The straight-line
method of depreciation is used for all property and equipment.
Property, plant and equipment consisted of the following:
Equipment
Equipment under customer usage agreements
Buildings and improvements
Leasehold improvements
Land
Furniture and fixtures
Finance lease right-of-use asset
Less - accumulated depreciation and
amortization
Estimated Useful Life
3–10 years
3–8 years
20–35 years
Shorter of the Original Term
of Lease
or Estimated Useful Life
5–7 years
September 24, 2022
September 25, 2021
$
$
394.8 $
486.5
196.0
44.8
40.9
16.7
7.5
1,187.2
(705.6)
481.6 $
467.1
484.6
191.2
49.7
41.3
16.8
9.9
1,260.6
(695.9)
564.7
Equipment under customer usage agreements primarily consists of diagnostic instruments located at customer sites but
owned by the Company. Generally, the customer has the right to use the equipment for a period of time provided they meet
certain agreed to conditions. The Company recovers the cost of providing the equipment from the sale of disposables, primarily
assays, tests and handpieces. The depreciation costs associated with equipment under customer usage agreements are charged to
cost of product revenues over the estimated useful life of the equipment. The costs to maintain the equipment in the field are
charged to cost of product revenue as incurred.
In September 2020 and October 2020, the Company was awarded grants of $7.6 million and $119.3 million, respectively,
from the Department of Defense Joint Acquisition Task Force ("DOD") to expand production capacity for the Company's two
SARS-CoV-2 assays. These grants are specifically to fund capital equipment and labor investments to increase manufacturing
capacity to enable the Company to provide a certain amount of COVID-19 tests per month for the U.S. market. The Company is
accounting for the funds received under these grants as a reimbursement of the purchased capital equipment. The Company
procures and pays for the capital equipment and necessary resources to build out its facility and construct the manufacturing
lines to meet the requirements specified in the grant agreement. Subsequent to the Company paying for the capital equipment,
the DOD will reimburse the Company upon it meeting certain requirements. However, the DOD retains title to assets purchased
under the agreement, and title is transferred to the Company upon meeting certain milestones of the manufacturing efforts and
obtaining approval from the DOD that the respective milestone has been met. As of September 24, 2022, the Company had
$20.5 million of capital equipment that was awaiting approval from the DOD pending completion of the defined milestones. In
fiscal 2022 and 2021, the Company received $75.0 million and $21.5 million, respectively, from the DOD for reimbursement of
capital equipment, which has been recorded as a reduction of the cost basis of the purchased equipment. In addition, a portion
of the DOD grant funds expenditures in connection with the project that don't qualify for capitalization and are recorded as a
reduction to expenses, which was $7.6 million and $1.3 million in fiscal 2022 and 2021, respectively. Payments under these
grants are subject to satisfaction of the conditions of the grants, including applicable governmental appropriations.
Long-Lived Assets
The Company reviews its long-lived assets, which includes property, plant and equipment and identifiable intangible
assets (see below for discussion of intangible assets), for impairment whenever events or changes in circumstances indicate that
the carrying amount of an asset may not be recoverable in accordance with ASC 360-10-35-15, Property, Plant and Equipment
—Impairment or Disposal of Long-Lived Assets (ASC 360). Recoverability of these assets is evaluated by comparing the
carrying value of the assets to the undiscounted cash flows estimated to be generated by those assets over their remaining
economic life. If the undiscounted cash flows are not sufficient to recover the carrying value of the assets, the assets are
considered impaired. The impairment loss is measured by comparing the fair value of the assets to their carrying value. Fair
value is determined by either a quoted market price, if any, or a value determined by a discounted cash flow technique.
Business Combinations and Acquisition of Intangible Assets
F-14
Table of Contents
The Company accounts for the acquisition of a business in accordance with ASC 805, Business Combinations (ASC 805).
Amounts paid to acquire a business are allocated to the assets acquired and liabilities assumed based on their fair values at the
date of acquisition. Contingent consideration not deemed to be linked to continuing employment is recorded at fair value on the
date of acquisition. The value recorded is based on estimates of future financial projections under various potential scenarios
using a Monte Carlo simulation. These cash flow projections are discounted with an appropriate risk adjusted rate. Each quarter
until such contingent amounts are earned, the fair value of the liability is remeasured and adjusted as a component of operating
expenses based on changes to the underlying assumptions. The estimates used to determine the fair value of the contingent
consideration liability are subject to significant judgment and actual results are likely to differ from the amounts originally
recorded. The Company determines the fair value of acquired intangible assets based on detailed valuations that use certain
information and assumptions provided by management. The Company allocates any excess purchase price over the fair value of
the net tangible and intangible assets acquired to goodwill.
The Company uses the income approach to determine the fair value of developed technology and in-process research and
development ("IPR&D") acquired in a business combination. This approach determines fair value by estimating the after-tax
cash flows attributable to the respective asset over its useful life and then discounting these after-tax cash flows back to a
present value. The Company bases its revenue assumptions on estimates of relevant market sizes, expected market growth rates,
expected trends in technology and expected product introductions by competitors. Developed technology represents patented
and unpatented technology and know-how. The value of the in-process projects is based on the project's stage of completion,
the complexity of the work completed as of the acquisition date, the projected costs to complete, the contribution of core
technologies and other acquired assets, the expected introduction date, the estimated cash flows to be generated upon
commercial release and the estimated useful life of the technology. The Company believes that the estimated developed
technology and IPR&D amounts represent the fair value at the date of acquisition and do not exceed the amount a third-party
would pay for the assets. The significant assumptions used to estimate the fair value of intangible assets include discount rates
and certain assumptions that form the basis of the forecasted results specifically revenue growth rates. These significant
assumptions are forward looking and could be affected by future economic and market conditions.
The Company also uses the income approach, as described above, to determine the estimated fair value of certain other
identifiable intangible assets including customer relationships, and trade names. Customer relationships represent established
relationships with customers, which provide a ready channel for the sale of additional products and services. Trade names
represent acquired company and product names.
Intangible Assets and Goodwill
Intangible Assets
Intangible assets are initially recorded at fair value and stated net of accumulated amortization and impairments. The
Company amortizes its intangible assets that have finite lives using either the straight-line method, or if reliably determinable,
based on the pattern in which the economic benefit of the asset is expected to be utilized. Amortization is recorded over the
estimated useful lives ranging from 5 to 30 years. The Company evaluates the recoverability of its definite lived intangible
assets whenever events or changes in circumstances or business conditions indicate that the carrying value of these assets may
not be recoverable based on expectations of future undiscounted cash flows for each asset group. If the carrying value of an
asset or asset group exceeds its undiscounted cash flows, the Company estimates the fair value of the assets, generally utilizing
a discounted cash flow analysis based on the present value of after-tax cash flows to be generated by the assets using a risk-
adjusted discount rate. To estimate the fair value of the assets, the Company uses market participant assumptions pursuant to
ASC 820, Fair Value Measurements.
Indefinite lived intangible assets, such as IPR&D assets, are initially recorded at fair value and are required to be tested
for impairment annually, or more frequently if indicators of impairment are present. The Company’s annual impairment test
date is as of the first day of its fourth quarter.
F-15
Table of Contents
Intangible assets consisted of the following:
Description
Acquired intangible assets:
Developed technology
In-process research and development
Customer relationships
Trade names
Total acquired intangible assets
Internal-use software
Capitalized software embedded in products
Total intangible assets
September 24, 2022
September 25, 2021
Gross
Carrying
Value
Accumulated
Amortization
Gross
Carrying
Value
Accumulated
Amortization
$
$
$
4,565.6 $
33.0
601.9
265.2
5,465.7 $
26.0
26.5
5,518.2 $
3,458.2 $
—
535.6
203.3
4,197.1 $
19.9
20.6
4,237.6 $
4,597.7 $
71.6
591.7
268.1
5,529.1 $
23.5
25.5
5,578.1 $
3,184.2
—
510.1
191.8
3,886.1
17.2
15.6
3,918.9
During the fourth quarter of fiscal 2022, the Company performed its annual impairment test of its only IPR&D
intangible asset, which was acquired in the Mobidiag Oy acquisition. The Company determined the fair value of the asset
utilizing a DCF model and recorded a $27.7 million impairment charge. The reduction in fair value was due to an increase in
the discount rate from higher interest rates, a reduction in forecasted revenues and timing of completing the project. During the
fourth quarter of fiscal 2022, the Company identified a certain product line associated with the Focal Therapeutics, Inc.
acquisition that would no longer be commercially sold. As a result, the Company recorded an impairment charge to write-off a
developed technology asset of $8.2 million. During the third quarter of fiscal 2022, the Company identified certain product
lines associated with the Faxitron Bioptics, LLC acquisition that would no longer be commercially sold. As a result, the
Company recorded an impairment charge to write-off the developed technology assets of $9.2 million. During the first quarter
of fiscal 2022, the Company acquired Bolder Surgical Holdings, Inc. and recorded $73.6 million of developed technology,
$21.7 million of customer relationships and $1.4 million of trade names based on its preliminary purchase accounting.
During the third quarter of fiscal 2021, the Company acquired Mobidiag and recorded $285.0 million of developed
technology, $74.0 million of in-process research and development, $20.9 million of customer relationships and $20.0 million of
trade names. During the second quarter of fiscal 2021, the Company acquired Biotheranostics, Inc. and recorded $160.3 million
of developed technology and $2.1 million of trade names. During the second quarter of fiscal 2021, the Company acquired
Diagenode SA and recorded $69.8 million of developed technology and $9.2 million of customer relationships. During the
second quarter of fiscal 2021, the Company acquired Somatex Medical Technologies GmbH and recorded $38.0 million of
developed technology, $1.2 million of customer relationships and $0.9 million of trade names.
Amortization expense related to developed technology is classified as cost of product revenues—amortization of
intangible assets. Amortization expense related to customer relationships, and trade names is classified as a component of
amortization of intangible assets within operating expenses.
The estimated amortization expense at September 24, 2022 for each of the five succeeding fiscal years was as follows:
Fiscal 2023
Fiscal 2024
Fiscal 2025
Fiscal 2026
Fiscal 2027
$
$
$
$
$
234.8
221.1
207.4
175.8
84.6
F-16
Table of Contents
Goodwill
In accordance with ASC 350, Intangibles—Goodwill and Other (ASC 350), the Company tests goodwill for impairment
annually at the reporting unit level and between annual tests if events and circumstances indicate it is more likely than not that
the fair value of a reporting unit is less than its carrying value. Events that could indicate impairment and trigger an interim
impairment assessment include, but are not limited to, current economic and market conditions, including a decline in market
capitalization, a significant adverse change in legal factors, business climate, operational performance of the business or key
personnel, and an adverse action or assessment by a regulator.
In performing the impairment test, the Company utilizes the single-step approach prescribed under Accounting Standards
Update No. 2017-04, Intangibles-Goodwill and Other (Topic 350): Simplifying the Test for Goodwill Impairment (ASU
2017-04). This approach requires a comparison of the carrying value of each reporting unit to its estimated fair value and to the
extent the carrying value exceeds the fair value a charge is recorded up to the amount of goodwill in the reporting unit. To
estimate the fair value of its reporting units, the Company primarily utilizes the income approach. The income approach is
based on a DCF analysis and calculates the fair value by estimating the after-tax cash flows attributable to a reporting unit and
then discounting the after-tax cash flows to present value using a risk-adjusted discount rate. Assumptions used in the DCF
require significant judgment, including judgment about appropriate discount rates and terminal values, growth rates, and the
amount and timing of expected future cash flows. The forecasted cash flows are based on the Company’s most recent budget
and strategic plan and for years beyond this period, the Company’s estimates are based on assumed growth rates expected as of
the measurement date. The Company believes its assumptions are consistent with the plans and estimates used to manage the
underlying businesses. The discount rates used are intended to reflect the risks inherent in future cash flow projections and are
based on estimates of the weighted-average cost of capital (“WACC”) of market participants. The market approach considers
comparable market data based on multiples of revenue or earnings before interest, taxes, depreciation and amortization
(“EBITDA”) and is primarily used as a corroborative analysis to the results of the DCF analysis. The Company believes its
assumptions used to determine the fair value of its reporting units are reasonable. If different assumptions were used,
particularly with respect to forecasted cash flows, terminal values, WACCs, or market multiples, different estimates of fair
value may result and there could be the potential that an impairment charge could result. Actual operating results and the related
cash flows of the reporting units could differ from the estimated operating results and related cash flows.
The Company conducted its fiscal 2022 impairment test for its reporting units on the first day of the fourth quarter, and as
noted above used DCF and market approaches to estimate the fair value of its reporting units as of June 26, 2022, and
ultimately used the fair value determined by the DCF approach in making its impairment test conclusions. As a result of
completing this analysis, all of the Company's reporting units had fair values exceeding their carrying values.
At September 24, 2022, the Company believes that its reporting units, with goodwill aggregating $3.2 billion, were not at
risk of failing the goodwill impairment test based on its current forecasts and qualitative assessment.
The Company conducted its fiscal 2021 and 2020 impairment tests for its reporting units on the first day of the fourth
quarter of its respective fiscal year, and as noted above used DCF and market approaches to estimate the fair value of its
reporting units as of the measurement date, and ultimately used the fair value determined by the DCF approach in making its
impairment test conclusions. The Company believes it used reasonable estimates and assumptions about future revenue, cost
projections, cash flows, market multiples and discount rates as of each measurement date. As a result of completing these
analyses, all of the Company's reporting units had fair values exceeding their carrying values.
A rollforward of goodwill activity by reportable segment from September 25, 2021 to September 24, 2022 is as follows:
Diagnostics
Breast Health
GYN Surgical
Skeletal Health
Total
Balance at September 25, 2021 $
Mobidiag acquisition
Bolder acquisition
Foreign currency and other
adjustments
Balance at September 24, 2022 $
1,410.8 $
(4.9)
—
797.1 $
—
—
1,065.6 $
—
68.8
8.1 $
—
—
3,281.6
(4.9)
68.8
(92.1)
1,313.8 $
(15.3)
781.8 $
(1.5)
1,132.9 $
(0.1)
8.0 $
(109.0)
3,236.5
Other Assets
Other assets consisted of the following:
F-17
Table of Contents
September 24, 2022
September 25, 2021
Other Assets
Tax receivable
Operating lease right of use
assets
Life insurance contracts
Deferred tax assets
Equity investments
Other
$
$
30.4 $
68.9
49.2
16.2
5.5
40.3
210.5 $
24.7
83.6
64.3
21.9
9.5
41.7
245.7
The right of use assets were recorded in connection with the adoption of ASC 842, Leases, and pertains to operating
leases. Life insurance contracts were purchased in connection with the Company’s Nonqualified Deferred Compensation Plan
(“DCP”) and are recorded at their cash surrender value (see Note 12 for further discussion).
Research and Software Development Costs
Costs incurred for the research and development of the Company’s products are expensed as incurred. Nonrefundable
advance payments for goods or services to be received in the future by the Company for use in research and development
activities are deferred. The deferred costs are expensed as the related goods are delivered or the services are performed.
The Company accounts for the development costs of software embedded in the Company’s products in accordance with
ASC 985, Software. Costs incurred in the research, design and development of software embedded in products to be sold to
customers are charged to expense until technological feasibility of the ultimate product to be sold is established. The
Company’s policy is that technological feasibility is achieved when a working model, with the key features and functions of the
product, is available for customer testing. Software development costs incurred after the establishment of technological
feasibility and until the product is available for general release are capitalized, provided recoverability is reasonably assured.
Capitalized software development costs are amortized over their estimated useful life and recorded within cost of revenues -
product.
Foreign Currency Translation
The financial statements of the Company’s foreign subsidiaries are translated in accordance with ASC 830, Foreign
Currency Matters. The reporting currency for the Company is the U.S. dollar. The functional currency of the Company’s
foreign subsidiaries is determined based on the guidance in ASC 830. The majority of the Company's foreign subsidiaries'
functional currency is the applicable local currency, although certain of the Company's foreign subsidiaries' functional currency
is the U.S. dollar based on the nature of their operations or functions. Assets and liabilities of subsidiaries whose functional
currency is the local currency are translated at the exchange rate in effect at each balance sheet date. Before translation, the
Company re-measures foreign currency denominated assets and liabilities, including inter-company accounts receivable and
payable, into the functional currency of the respective entity, resulting in unrealized gains or losses recorded in other income
(expense), net in the Consolidated Statements of Income. Revenues and expenses are translated using average exchange rates
during the respective period. Foreign currency translation adjustments are accumulated as a component of other comprehensive
income (loss), which is a separate component of stockholders’ equity. Gains and losses arising from transactions denominated
in foreign currencies are included in other income (expense), net in the Consolidated Statements of Income. During fiscal years
2022, 2021 and 2020, the Company recorded net foreign exchange gains (losses) of $48.5 million, $(15.1) million, and
$3.4 million, respectively.
Accumulated Other Comprehensive Income (Loss)
Other comprehensive income (loss) includes certain transactions that have generally been reported in the statement of
stockholders’ equity. The following tables summarize the components and changes in accumulated balances of other
comprehensive loss for the periods presented:
F-18
Table of Contents
Year Ended September 24, 2022
Year Ended September 25, 2021
Foreign
Currency
Translation
Pension
Plans
Hedged
Interest
Rate
Swaps
Foreign
Currency
Translation
Pension
Plans
Hedged
Interest
Rate Caps
Total
Hedged
Interest
Rate
Swaps
Total
Beginning Balance
$
(43.1) $
(1.3) $
(14.7) $
(59.1) $
(22.9) $
(1.8) $
(0.9) $
(24.1) $
(49.7)
Other comprehensive income
(loss) before reclassifications
Charges reclassified to statement
of operations
(224.1)
—
1.0
—
44.0
(179.1)
(20.2)
—
—
—
0.5
—
0.4
0.5
9.4
—
(9.9)
0.5
Ending Balance
$
(267.2) $
(0.3) $
29.3 $
(238.2) $
(43.1) $
(1.3) $
— $
(14.7) $
(59.1)
Derivatives
Interest Rate Risk - Cash Flow Hedge
The Company is exposed to certain risks arising from both its business operations and economic conditions. The
Company manages its exposure to some of its interest rate risk through the use of interest rate swaps, which are derivative
financial instruments. The Company does not use derivatives for speculative purposes. For a derivative that is designated as a
cash flow hedge, changes in the fair value of the derivative are recognized in accumulated other comprehensive income
("AOCI") to the extent the derivative is effective at offsetting the changes in the cash flows being hedged until the hedged item
affects earnings.
During fiscal 2018, the Company entered into separate interest rate cap agreements with multiple counter-parties to
mitigate the interest rate volatility associated with the variable interest rate on its amounts borrowed under the term loan feature
of its credit facilities (see Note 7). Interest rate cap agreements provide the right to receive cash if the reference interest rate
rises above a contractual rate. During fiscal 2019, the Company entered into additional separate interest rate cap agreements
with multiple counter-parties to extend the expiration date of its hedges by an additional year.
The critical terms of the interest rate caps were designed to mirror the terms of the Company’s LIBOR-based borrowings
under its Credit Agreement, that has been amended multiple times, and therefore were highly effective at offsetting the cash
flows being hedged. The Company designated these derivatives as cash flow hedges of the variability of the LIBOR-based
interest payments on $1.0 billion of principal, which ended on December 27, 2019 (the first quarter of fiscal 2020) for the
contracts entered into in fiscal 2018, and on December 23, 2020 (the first quarter of fiscal 2021) for the interest rate cap
agreements entered into in fiscal 2019.
During fiscal 2021 and 2020, interest expense of $0.5 million and $2.3 million, respectively, was reclassified from AOCI
to the Company's Consolidated Statements of Income related to the interest rate cap agreements. The last interest rate cap
agreement matured as of December 26, 2020.
In fiscal 2019, in order to hedge a portion of its variable rate debt, the Company entered into an interest rate swap contract
with an effective date of December 23, 2020 and a termination date of December 17, 2023. On August 25, 2022, the interest
rate swap agreement (consistent with the Company's Credit Agreement; see Note 7) was restructured to convert the benchmark
interest rate from LIBOR to the SOFR rate effective September 23, 2022 with a termination date of December 17, 2023. The
Company applied the practical and optional expedients in ASC 848, Reference Rate Reform, in evaluating the impact of
modifying the contract, which resulted in no change to the accounting for this derivative contract. The notional amount of this
swap is $1.0 billion. The restructured interest rate swap effectively fixes the SOFR component of the variable interest rate on
$1.0 billion of the notional amount under the 2021 Credit Agreement at 1.23%. The critical terms of the restructured interest
rate swap are designed to mirror the terms of the Company’s SOFR-based borrowings under its credit agreement and therefore
are highly effective at offsetting the cash flows being hedged. The Company designated this derivative as a cash flow hedge of
the variability of the SOFR-based interest payments on $1.0 billion of principal. Therefore, changes in the fair value of the
swap are recorded in AOCI and net of taxes were a gain of $44.0 million, a gain of $9.4 million and a loss of $27.6 million for
fiscal years 2022, 2021, and 2020, respectively. The fair value of this derivative was in an asset position of $38.9 million as of
September 24, 2022.
Forward Foreign Currency Contracts and Foreign Currency Option Contracts
The Company enters into forward foreign currency exchange contracts and foreign currency option contracts to mitigate
certain operational exposures from the impact of changes in foreign currency exchange rates. Such exposures result from the
portion of the Company's cash and operations that are denominated in currencies other than the U.S. dollar, primarily the Euro,
the UK Pound, the Australian dollar, the Canadian dollar, the Chinese Yuan and the Japanese Yen. These foreign currency
exchange contracts are entered into to support transactions made in the ordinary course of business and are not speculative in
nature. The contracts are generally for periods of one year or less. The Company did not elect hedge accounting for these
contracts; however, the Company may seek to apply hedge accounting in future scenarios. The change in the fair value of these
contracts is recognized directly in earnings as a component of other income, net.
F-19
Table of Contents
September 24, 2022
September 25, 2021
September 26, 2020
Years Ended
Amount of realized (loss) gain recognized in income
Forward foreign currency contracts
Foreign currency option contracts
Amount of unrealized (loss) gain recognized in income
Forward foreign currency contracts
Foreign currency option contracts
Amount of gain (loss) recognized in income
Total
$
$
$
$
$
68.5 $
—
68.5 $
14.7 $
5.5
20.2 $
(3.6) $
(6.1)
(9.7) $
0.5 $
(4.0)
(3.5) $
88.7 $
(13.2) $
0.7
(1.9)
(1.2)
(0.2)
4.0
3.8
2.6
As of September 24, 2022, the Company had outstanding forward foreign currency contracts that were not designated for
hedge accounting and are used to hedge fluctuations in the U.S. dollar of certain of the Company's cash balances denominated
in the Euro and UK pound, as well as forecasted transactions denominated in the Euro, UK pound, Australian Dollar, Canadian
Dollar, Chinese Yuan and Japanese Yen with an aggregate notional amount of $458.1 million.
Financial Instrument Presentation
The table below presents the fair value of the Company's derivative financial instruments as well as their classification on
the balance sheet as of September 24, 2022:
Balance Sheet Location
September 24, 2022
September 25, 2021
Assets:
Derivative instrument designated as a cash flow hedge:
Interest rate swap contract
Prepaid expenses and
other current assets
Interest rate swap contract
Other assets
Derivatives not designated as hedging instruments:
Forward foreign currency contracts
Foreign currency option contracts
Prepaid expenses and
other current assets
Prepaid expenses and
other current assets
Liabilities:
Derivative instruments designated as a cash flow hedge:
Interest rate swap contract
Interest rate swap contract
Total
Accrued expenses
Other long-term
liabilities
Derivatives not designated as hedging instruments:
Forward foreign currency contracts
Accrued expenses
$
$
$
$
$
$
$
31.9 $
7.0
38.9 $
15.8 $
10.6
26.4 $
— $
—
— $
— $
—
—
—
1.7
—
1.7
11.1
7.6
18.7
0.6
The following table presents the unrealized gain (loss) recognized in AOCI related to the interest rate caps and interest
rate swap for the following reporting periods:
F-20
Table of Contents
Amount of gain (loss) recognized in other
comprehensive income (loss), net of taxes:
Interest rate swap
Interest rate cap agreements
Total
September 24,
2022
Years Ended
September 25,
2021
September 26,
2020
$
$
44.0 $
—
44.0 $
9.4 $
0.4
9.8 $
(27.6)
(0.5)
(28.1)
Trade Receivables and Allowance for Credit Losses
Effective September 27, 2020, the Company adopted ASU No. 2016-13, Financial Instruments - Credit Losses (Topic
326), which requires that financial assets measured at amortized cost be presented at the net amount expected to be collected.
The expected credit losses are developed using an estimated loss rate method that considers historical collection experience,
current conditions, and reasonable and supportable forecasts that affect the collectability of the reported amount. The estimated
loss rates are applied to trade receivables with similar risk characteristics such as the length of time the balance has been
outstanding and the location of the customer. In certain instances, the Company may identify individual trade receivable assets
that do not share risk characteristics with other trade receivables, in which case the Company records its expected credit losses
on an individual asset basis. For example, potential adverse changes to customer liquidity from new macroeconomic events,
such as the COVID-19 pandemic, must be taken into consideration. To date, the Company has not experienced significant
customer payment defaults, or identified other significant collectability concerns as a result of the COVID-19 pandemic. In
connection with assessing credit losses for individual trade receivable assets, the Company considers significant factors relevant
to collectability including those specific to the customer such as bankruptcy, length of time an account is outstanding, and the
liquidity and financial position of the customer. If a trade receivable asset is evaluated on an individual basis, the Company
excludes those assets from the portfolios of trade receivables evaluated on a collective basis.
The following is a rollforward of the allowance for credit losses for fiscal 2022, 2021 and 2020:
Period Ended:
September 24, 2022
September 25, 2021
September 26, 2020
Balance at
Beginning
of Period
Charged to
Costs and
Expenses
Divested
Write-
offs and
Payments
Balance at
End of
Period
$
$
$
40.5 $
31.6 $
17.8 $
3.4 $
15.0 $
26.8 $
— $
— $
(5.8) $
(6.2) $
(6.1) $
(7.2) $
37.7
40.5
31.6
Cost of Service and Other Revenues
Cost of service and other revenues primarily represents payroll and related costs associated with the Company’s
professional services, employees, consultants, infrastructure costs and overhead allocations, including depreciation, rent and
materials consumed in providing the service.
Stock-Based Compensation
The Company accounts for share-based payments in accordance with ASC 718, Stock Compensation (ASC 718). As
such, all share-based payments to employees, including grants of stock options, restricted stock units, performance stock units
and market stock units and shares issued under the Company’s employee stock purchase plan, are recognized in the
Consolidated Statements of Income based on their fair values on the date of grant. In addition, all excess tax benefits and
deficiencies are recognized as a component of the provision for income taxes on a discrete basis in the period in which the
equity awards vest and/or are settled.
Net Income Per Share
Basic net income per share is computed by dividing net income by the weighted average number of common shares
outstanding. Diluted net income per share is computed by dividing net income by the weighted average number of common
shares and the dilutive effect of potential future issuances of common stock from outstanding stock options and restricted stock
units for the period outstanding determined by applying the treasury stock method. In accordance with ASC 718, the assumed
proceeds under the treasury stock method include the average unrecognized compensation expense of in-the-money stock
options and restricted stock units. This results in the assumed buyback of additional shares, thereby reducing the dilutive impact
of equity awards.
F-21
Table of Contents
A reconciliation of basic and diluted share amounts for fiscal 2022, 2021, and 2020 was as follows:
Basic weighted average common shares outstanding
Weighted average common stock equivalents from
assumed exercise of stock options and restricted stock
units
Diluted weighted average common shares outstanding
Weighted-average anti-dilutive shares related to:
September 24, 2022
September 25, 2021
September 26, 2020
251,527
257,046
262,727
2,318
253,845
2,660
259,706
1,886
264,613
Outstanding stock options and restricted stock units
1,049
528
1,158
Product Warranties
The Company generally offers a one-year warranty for its products. The Company provides for the estimated cost of
product warranties at the time product revenue is recognized. Factors that affect the Company’s warranty reserves include the
number of units sold, historical and anticipated rates of warranty repairs and the cost per repair. The Company periodically
assesses the adequacy of the warranty reserve and adjusts the amount as necessary.
Product warranty activity for fiscal 2022 and 2021 was as follows:
Period ended:
September 24, 2022
September 25, 2021
Advertising Costs
Balance at
Beginning of
Period
Provisions
Acquired
Settlements/
Adjustments
Balance at End
of Period
$
$
8.8
9.9
$
$
6.3 $
7.7 $
—
0.3
$
$
(7.1) $
(9.1) $
8.0
8.8
Advertising costs are charged to operations as incurred. The Company does not have any direct-response advertising.
Advertising costs, which include trade shows and conventions, were approximately $78.1 million, $9.8 million and $15.6
million for fiscal 2022, 2021 and 2020, respectively, and were included in selling and marketing expense in the Consolidated
Statements of Income. The increase in advertising costs in fiscal 2022 was primarily due to the Company's agreement to be a
sponsor of the Women's Tennis Association and the production and running of its Super Bowl commercial.
New Accounting Pronouncements
In December 2019, the FASB issued ASU No. 2019-12, Income Taxes (Topic 740) Simplifying the Accounting for Income
Taxes. The FASB issued this Update as part of its initiative to reduce complexity in accounting standards (the Simplification
Initiative). For public business entities, the amendments in this Update are effective for fiscal years, and interim periods within
those fiscal years, beginning after December 15, 2020, and are applicable to the Company in fiscal 2022. The adoption of ASU
No. 2019-12 did not have a material impact on the Company's consolidated financial position and results of operations.
In January 2020, the FASB issued ASU No. 2020-01, Investments - Equity Securities (Topic 321), Investments - Equity
Method and Joint Ventures (Topic 323), and Derivatives and Hedging (Topic 815). The FASB issued this Update to clarify
certain interactions between the guidance to account for certain equity securities under Topic 321, the guidance to account for
investments under the equity method of accounting in Topic 323, and the guidance in Topic 815. This update could change how
an entity accounts for an equity security under the measurement alternative or a forward contract or purchased option to
purchase securities that, upon settlement of the forward contract or exercise of the purchased option, would be accounted for
under the equity method of accounting or the fair value option in accordance with Topic 825, Financial Instruments. For
entities that have adopted the amendments in Update 2020-01, the updated guidance is effective for annual periods beginning
after December 15, 2020, and is applicable to the Company in fiscal 2022. The adoption of ASU No. 2020-01 did not have a
material impact on the Company's consolidated financial position and results of operations.
In January 2020, the FASB issued ASU No. 2020-04, Reference Rate Reform (Topic 848). The FASB issued this Update
as optional guidance for a limited period of time to ease the potential burden in accounting for or recognizing the effects of
reference rate reform on financial reporting. This update will provide optional expedients and exceptions for applying GAAP to
only contracts, hedging relationships, and other transactions that reference LIBOR or another reference rate expected to be
F-22
Table of Contents
discontinued because of reference rate reform. For entities that have adopted the amendments in Update 2020-04, the updated
guidance is effective for all entities as of March 12, 2020 through December 31, 2022. The Company adopted ASU 2020-04 in
the first quarter of fiscal 2022, which did not have a material impact on the Company's consolidated financial position and
results of operations.
In January 2021, FASB issued ASU No. 2021-01, Reference Rate Reform (Topic 848) Scope. The FASB issued this
Update in response to stakeholder concerns about potential diversity in practice. The FASB decided to clarify the scope of
Topic 848 so that derivatives affected by the discounting transition are explicitly eligible for certain optional expedients and
exceptions in Topic 848. This update provides optional expedients and exceptions for applying generally accepted accounting
principles (GAAP) to only contracts, hedging relationships, and other transactions that reference LIBOR or another reference
rate expected to be discontinued because of reference rate reform. For entities that have adopted the amendments in Update
2021-01, the updated guidance is effective for all entities immediately as of January 2021. The Company adopted ASU 2021-01
in the first quarter of fiscal 2022, which did not have a material impact on the Company's consolidated financial position and
results of operations.
In May 2021, the FASB issued ASU No. 2021-05, Leases (Topic 842), Lessors - Certain Leases with Variable Lease
Payments. This Update addresses an issue related to a lessor's accounting for certain leases with variable lease payments. The
amendments in this Update affect lessors with lease contracts that (1) have variable lease payments that do not depend on a
reference index or a rate and (2) would have resulted in the recognition of a selling loss at lease commencement if classified as
a sales-type lease or a direct financing lease. The Company adopted the amendments in ASU No. 2021-05 in the first quarter of
fiscal 2022, which did not have a material effect on the Company's consolidated financial statements.
3. Revenue
The Company accounts for revenue pursuant to ASC 606, Revenue from Contracts with Customer (ASC 606) and
generates revenue from the sale of its products, primarily medical imaging systems and related components and software,
diagnostic tests and assays and surgical disposable products, and related services, which are primarily support and maintenance
services on its medical imaging systems, and to a lesser extent installation, training and repairs. In addition, the Company
generates service revenue from performing laboratory testing services acquired in its Biotheranostics, Inc. acquisition, which is
included in its Molecular Diagnostics business. The Company's products are sold primarily through a direct sales force, and
within international markets, there is more reliance on distributors and resellers. Revenue is recorded net of sales tax. The
following table provides revenue from contracts with customers by business and geographic region on a disaggregated basis:
F-23
Table of Contents
Business (in
millions)
Diagnostics:
Cytology &
Perinatal
Molecular
Diagnostics
Blood
Screening
September 24, 2022
September 25, 2021
September 26, 2020
United
States
Intl.
Total
United
States
Intl.
Total
United
States
Intl.
Total
Years Ended
$ 300.4 $ 174.3 $ 474.7 $ 304.6 $ 169.3 $ 473.9 $ 266.3 $ 143.8 $ 410.1
1,694.5
816.9 2,511.4
2,038.9 1,132.6 3,171.5
1,272.5
375.9 1,648.4
32.4
—
32.4
49.6
—
49.6
43.6
—
43.6
Total
2,027.3
991.2 3,018.5
2,393.1 1,301.9 3,695.0
1,582.4
519.7 2,102.1
Breast Health:
Breast
Imaging
Interventional
Breast
Solutions
735.1
216.5
951.6
830.4
253.0 1,083.4
722.0
231.6
953.6
222.1
54.1
276.2
221.4
47.5
268.9
166.6
31.7
198.3
Total
957.2
270.6 1,227.8
1,051.8
300.5 1,352.3
888.6
263.3 1,151.9
GYN Surgical
423.8
99.1
522.9
396.4
91.7
488.1
310.1
66.0
376.1
Skeletal Health
59.6
34.0
93.6
61.0
35.9
96.9
51.2
29.8
81.0
Medical Aesthetics
—
—
—
—
—
—
30.9
34.4
65.3
Total
$ 3,467.9 $ 1,394.9 $ 4,862.8 $ 3,902.3 $ 1,730.0 $ 5,632.3 $ 2,863.2 $ 913.2 $ 3,776.4
Geographic Regions (in millions)
September 24,
2022
September 25,
2021
September 26,
2020
Years Ended
United States
Europe
Asia-Pacific
Rest of World
$
3,467.9 $
888.5
359.7
146.7
3,902.3 $
1,201.8
365.0
163.2
2,863.2
569.8
226.8
116.6
$
4,862.8 $
5,632.3 $
3,776.4
The following table provides revenue recognized by source:
Revenue by type (in millions)
Disposables
Capital equipment,
components and software
Service
Other
Years Ended
September 24,
2022
September 25,
2021
September 26,
2020
$
3,603.6 $
4,198.2 $
2,561.1
587.6
652.4
19.2
4,862.8 $
769.1
598.1
66.9
5,632.3 $
665.9
516.6
32.8
3,776.4
$
The Company considers revenue to be earned when all of the following criteria are met: the Company has a contract with
a customer that creates enforceable rights and obligations; promised products or services are identified; the transaction price, or
the amount the Company expects to receive, including an estimate of uncertain amounts subject to a constraint to ensure
revenue is not recognized in an amount that would result in a significant reversal upon resolution of the uncertainty, is
F-24
Table of Contents
determinable; and the Company has transferred control of the promised items to the customer. A performance obligation is a
promise in a contract to transfer a distinct good or service to the customer and is the unit of account in the contract. The
transaction price for the contract is measured as the amount of consideration the Company expects to receive in exchange for
the goods and services expected to be transferred. A contract's transaction price is allocated to each distinct performance
obligation and recognized as revenue when, or as, control of the distinct good or service is transferred. Transfer of control for
the Company's products is generally at shipment or delivery, depending on contractual terms, but occurs when title and risk of
loss transfers to the customer which represents the point in time when the customer obtains the use of and substantially all of
the remaining benefit of the product. As such, the Company's performance obligation related to product sales is satisfied at a
point in time. Revenue from support and maintenance contracts, extended warranty and professional services for installation,
training and repairs is recognized over time based on the period contracted or as the services are performed as these methods
represent a faithful depiction of the transfer of goods and services.
The Company recognizes a receivable when it has an unconditional right to payment, which represents the amount the
Company expects to collect in a transaction and is most often equal to the transaction price in the contract. Payment terms are
typically 30 days in the U.S. but may be longer in international markets. The Company treats shipping and handling costs
performed after a customer obtains control of the good as a fulfillment cost and records these costs within costs of product
revenue when the corresponding revenue is recognized.
The Company also places instruments (or equipment) at customer sites but retains title to the instrument. The customer
has the right to use the instrument for a period of time, and the Company recovers the cost of providing the instrument through
the sales of disposables, namely tests and assays in Diagnostics and handpieces in GYN Surgical. These types of agreements
include an embedded lease, which is generally an operating lease, for the right to use an instrument and no instrument revenue
is recognized at the time of instrument delivery. The Company recognizes a portion of the revenue allocated to the embedded
lease concurrent with the sale of disposables over the term of the agreement.
Revenue from laboratory testing services, which are generated by the Company's Biotheranostics acquisition, is
recognized based upon contracted amounts with payors and historical cash collection experience for the same test or same
payor group. Revenue is recognized once the laboratory services have been performed, the results have been delivered to the
ordering physician, the payor has been identified, and insurance has been verified. The estimated timeframes for cash collection
are three months for Medicare payors, six months for Medicare Advantage payors, and nine months for commercial payors.
Some of the Company's contracts have multiple performance obligations. For contracts with multiple performance
obligations, the Company allocates the transaction price to each performance obligation using its best estimate of the standalone
selling price of each distinct good or service in the contract. The Company determines its best estimate of standalone selling
price using average selling prices over 3- to 12-month periods of data depending on the products or nature of the services
coupled with current market considerations. If the product or service does not have a history of sales or if sales volume is not
sufficient, the Company relies on prices set by its pricing committees or applicable marketing department adjusted for expected
discounts.
Variable Consideration
The Company exercises judgment in estimating variable consideration, which includes volume discounts, sales rebates,
product returns and other adjustments. These amounts are recorded as a reduction to revenue and classified as a current liability.
The Company bases its estimates for volume discounts and sales rebates on historical information to the extent it is reasonable
to be used as a predictive tool of expected future rebates. To the extent the transaction price includes variable consideration, the
Company applies judgment in constraining the estimated variable consideration due to factors that may cause reversal of
revenue recognized. The Company evaluates constraints based on its historical and projected experience with similar customer
contracts. The Company's contracts for the sale of capital equipment and related components, and assays and tests typically do
not provide the right to return product, however, its contracts for the sale of its GYN Surgical and Interventional Breast
Solutions surgical handpieces provide for a right of return for a limited period of time. In general, estimates of variable
consideration and constraints are not material to the Company's financial statements.
Remaining Performance Obligations
As of September 24, 2022, the estimated revenue expected to be recognized in the future related to performance
obligations that are unsatisfied was approximately $867.6 million. These remaining performance obligations primarily relate to
support and maintenance obligations and extended warranty in the Company's Breast Health and Skeletal Health reportable
segments. The Company expects to recognize approximately 43% of this amount as revenue in 2023, 29% in 2024, 17% in
2025, 8% in 2026, and 3% thereafter. As permitted, the Company does not include remaining performance obligations related
to contracts with original expected durations of one year or less in the amounts above.
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Table of Contents
Contract Assets and Liabilities
The Company discloses accounts receivable separately in the Consolidated Balance Sheets at their net realizable value.
Contract assets primarily relate to the Company's conditional right to consideration for work completed but not billed at the
reporting date. Contract assets at the beginning and end of the period, as well as the changes in the balance, were immaterial.
Contract liabilities primarily relate to payments received from customers in advance of performance under the contract.
The Company records a contract liability, or deferred revenue, when it has an obligation to provide service, and to a much
lesser extent product, to the customer and payment is received or due in advance of performance. Deferred revenue primarily
relates to support and maintenance contracts and extended warranty obligations within the Company's Breast Health and
Skeletal Health reportable segments. Contract liabilities are classified as other current liabilities and other long-term liabilities
on the Consolidated Balance Sheets. The Company recognized revenue of $119.7 million and $112.1 million in the years ended
September 24, 2022 and September 25, 2021, respectively, that was included in the contract liability balance at September 25,
2021 and September 26, 2020, respectively.
Practical Expedients
The Company applies a practical expedient to expense costs to obtain a contract with a customer as incurred when the
amortization period would have been one year or less. These costs solely comprise sales commissions and typically the
commissions are incurred at the time of shipment of product and upon billings for support and maintenance contracts.
4. Leases
In February 2016, the FASB issued ASU No. 2016-02, Leases (Topic 842), referred to as ASC 842. The purpose of ASU
2016-02 was to increase the transparency and comparability among organizations by recognizing lease assets and liabilities on
the balance sheet, including those previously classified as operating leases under GAAP, and disclosing key information about
leasing arrangements. ASC 842, as amended, was effective for the Company in fiscal 2020. The Company adopted the standard
using the transition method provided by ASC Update No. 2018-11, Leases (Topic 842): Targeted Improvements. Under this
method, the Company applied the new lease standard on September 29, 2019, rather than at the earliest comparative period
presented in the financial statements.
Upon transition, the Company applied the package of practical expedients permitted under ASC 842 transition guidance to
its entire lease portfolio at September 29, 2019. As a result, the Company was not required to reassess (i) whether any expired
or existing contracts are or contain leases, (ii) the classification of any expired or existing leases, and (iii) initial direct costs for
any existing leases. Furthermore, as a lessee the Company elected to combine lease and non-lease components together for the
majority of its leases. As a result, for these applicable classes of underlying assets, the Company accounted for each separate
lease component and the non-lease components associated with that lease component as a single lease component.
Under ASC 842 as a lessor, in instances where the Company places instruments (or equipment) at customer sites as part of
its reagent rental contracts, certain of the Company's reagent rental contracts could be classified as sales-type leases. Under
sales-type leases, there is accelerated expense recognition for the cost of the placed equipment and potentially up-front revenue
in the event there are fixed rental payments, a portion of which would be allocated to the equipment. The Company does not
have a significant amount of sales-type leases. Prior to the adoption of ASC 842, all instruments placed under the Company's
reagent rental programs were classified as operating leases and instrument revenue and cost were recognized over the term of
the contract.
Lessee Activity - Leases where Hologic is the Lessee
The majority of the Company's facilities are occupied under operating lease arrangements with various expiration dates
through 2035, some of which include options to extend the term of the lease, and some of which include options to terminate
the lease within one year. The Company has operating leases for office space, land, warehouse and manufacturing space,
vehicles and certain equipment. Leases with an initial term of 12 months or less are generally not recorded on the balance sheet
and expense for these leases is recognized on a straight-line basis over the lease term. For leases executed in fiscal 2020 and
later, the Company accounts for the lease components and the non-lease components as a single lease component. The
Company's leases have remaining lease terms of one year to approximately 13 years, some of which may include options to
extend the leases for up to 10 years and some include options to terminate early. These options have been included in the
F-26
Table of Contents
determination of the lease liability when it is reasonably certain that the option will be exercised. The Company does not have
any leases that include residual value guarantees.
The Company determines whether an arrangement is or contains a lease based on the unique facts and circumstances
present at the inception of an arrangement. The right-of-use assets and related liabilities for operating leases are included in
other assets, accrued expenses, and other long-term liabilities in the consolidated balance sheet as of September 24, 2022.
Right-of-use assets represent the Company's right to use an underlying asset for the lease term and lease liabilities
represent the Company's obligation to make lease payments arising from the lease contract. Operating and finance lease
liabilities and their corresponding right-of-use assets are recorded based on the present value of fixed lease payments over the
expected lease term. The interest rate implicit in lease contracts is typically not readily determinable. As such, the Company
utilizes the incremental borrowing rate, which is the estimated rate that would be incurred to borrow on a collateralized basis
over a similar term at an amount equal to the lease payments in a similar economic environment. The weighted average
discount rate utilized on the Company's operating and finance lease liabilities as of September 24, 2022 was 1.97%.
The following table presents supplemental balance sheet information related to the Company's operating and finance
leases:
Balance Sheet Location
Operating Leases Finance Leases Operating Leases Finance Leases
September 24, 2022
September 25, 2021
Assets
Lease right-of-use assets
Finance lease right-of-use
assets (non-current)
Liabilities
Operating lease liabilities
(current)
Finance lease liabilities
(current)
Operating lease liabilities
(non-current)
Finance lease liabilities (non-
current)
Other assets
Property, plant and
equipment, net
Accrued expenses
Finance lease obligations -
short term
Other long-term liabilities
Finance lease obligations -
long term
$
$
$
$
$
$
68.9 $
— $
83.6 $
— $
6.0 $
— $
23.2 $
— $
26.8 $
— $
3.2 $
— $
53.8 $
— $
66.1 $
—
9.3
—
3.7
—
— $
18.0 $
— $
22.8
In connection with the Diagenode SA acquisition, the Company acquired two finance leases. The Company accounted for
these lease agreements pursuant to ASC 842 and ASC 805 and recorded both an asset and liability at the present value of future
lease payments as part of the purchase accounting. The finance leases are for two facilities with remaining lease terms of 7 and
11 years and contain a bargain purchase option of 3% at the end of the lease term.
The following table presents the weighted average remaining lease term and discount rate information related to the
Company's operating and finance leases:
Weighted average remaining lease term
Weighted average discount rate
4.51
1.3 %
6.53
4.3 %
4.95
1.6 %
7.52
4.3 %
As of September 24, 2022
As of September 25, 2021
Operating Leases
Finance Lease
Operating Leases
Finance Lease
The following table provides information related to the Company’s operating and finance leases:
F-27
Table of Contents
Year Ended
September 24, 2022
Year Ended
September 25, 2021
Operating lease cost (a)
Finance lease cost - amortization of right-of-use assets
Finance lease cost - interest cost
Cash paid for amounts included in the measurement of lease liabilities:
Operating cash flows from finance leases
Operating cash flows from operating leases
Financing cash flows from finance leases
Total cash paid for amounts included in the measurement of lease
liabilities
ROU assets arising from entering into new operating lease obligations
ROU assets arising from entering into new finance lease obligations
$
$
$
$
$
$
$
$
$
28.6 $
0.8 $
1.0 $
1.0 $
29.3 $
3.3 $
33.6 $
16.6 $
— $
30.1
0.6
1.0
1.0
28.2
2.4
31.6
28.6
9.1
(a) Includes short-term lease expense and variable lease costs, which were immaterial for the year ended September 24,
2022.
The following table presents the future minimum lease payments under non-cancellable operating lease liabilities and
finance lease as of September 24, 2022:
Fiscal Year
2023
2024
2025
2026
2027
Thereafter
Total future minimum lease payments
Less: imputed interest
Present value of lease liabilities
Lessor Activity - Leases where Hologic is the Lessor
Operating Leases
Finance Leases
$
$
24.2 $
19.5
14.0
8.8
6.2
6.8
79.5
(2.5)
77.0 $
4.0
3.8
3.7
3.7
3.9
4.9
24.0
(2.8)
21.2
Certain assets, primarily diagnostics instruments, are leased to customers under contractual arrangements that typically
include an operating lease and performance obligations for disposables, reagents and other consumables. These contractual
arrangements are subject to termination provisions which are evaluated in determining the lease term for lease accounting
purposes. Contract terms vary by customer and may include options to terminate the contract or options to extend the contract.
Where instruments are provided under operating lease arrangements, some portion or the entire lease revenue may be variable
and subject to subsequent non-lease component (e.g., reagent) sales. Sales-type leases are immaterial. The allocation of revenue
between the lease and non-lease components is based on stand-alone selling prices. Lease revenue represented less than 3% of
the Company’s consolidated revenue for all periods presented.
In connection with the disposition of the Medical Aesthetics business in fiscal 2020, the Company entered into an
agreement to sublease to Cynosure its U.S. headquarters and manufacturing location. As such, the Company derecognized
$10.2 million for the right-of-use asset for the finance lease and recorded a lease receivable, which is $15.2 million as of
September 24, 2022.
The Company leases a portion of a building it owns and subleases some of its rented facilities and has received aggregate
rental income of $2.8 million, $2.6 million and $2.0 million in fiscal 2022, 2021 and 2020, respectively, which has been
recorded as an offset to operating lease costs. The future minimum annual rental income payments under these lease and
sublease agreements at September 24, 2022 are as follows:
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Table of Contents
Fiscal 2023
Fiscal 2024
Fiscal 2025
Fiscal 2026
Fiscal 2027
Thereafter
Total
5. Business Combinations
$
$
2.7
2.5
1.7
0.8
0.9
1.3
9.9
During fiscal 2022, 2021, and 2020, the Company completed several business combinations for a total consideration of
$160.1 million, $1,178.9 million, and $269.0 million, respectively. The business combinations resulted in the recognition of
intangible assets, goodwill and other assets and liabilities summarized below. During 2021, the Company also completed an
asset acquisition of customer relationship assets of $5.6 million.
Fiscal 2022 Acquisitions
Bolder Surgical
On November 29, 2021, the Company completed the acquisition of Bolder Surgical Holdings, Inc. ("Bolder"), for a
purchase price of $160.1 million. Bolder, located in Louisville, Colorado, is a developer and manufacturer of energy vessel
sealing surgical devices used in both laparoscopic and open procedures. Bolder's results of operations are reported in the
Company's GYN Surgical reportable segment from the date of acquisition.
The total purchase price was allocated to Bolder's preliminary tangible and identifiable intangible assets and liabilities
based on the estimated fair values as of November 29, 2021, as set forth below.
Cash
Accounts receivable
Inventory
Other assets
Accounts payable and accrued expenses
Identifiable intangible assets:
Developed technology
Customer relationship
Trade names
Deferred income taxes, net
Goodwill
Purchase Price
$
$
1.9
1.3
3.3
3.0
(3.2)
73.6
21.7
1.4
(11.7)
68.8
160.1
In performing the preliminary purchase price allocation, the Company considered, among other factors, the intended
future use of acquired assets, analysis of historical financial performance and estimates of future performance of Bolder's
business. The allocation of the purchase price is preliminary as the Company continues to gather information supporting the
acquired assets and liabilities, including, but not limited to, deferred income taxes.
As part of the preliminary purchase price allocation, the Company determined the identifiable intangible assets are
developed technology, customer relationships and trade names. The preliminary fair value of the intangible assets was
estimated using the income approach, and the cash flow projections were discounted using a 16.0% rate. The cash flows were
based on estimates used to price the transaction, and the discount rate applied was benchmarked with reference to the implied
rate of return from the transaction model and the weighted average cost of capital.
The developed technology assets are comprised of know-how, patents and technologies embedded in Bolder's products
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and relate to currently marketed products. The developed technology assets comprise the primary product families under the
JustRight and CoolSeal technology platforms.
The preliminary estimate of the weighted average life for the developed technology, customer relationship, and trade
name assets is 10 years. The preliminary calculation of the excess of the purchase price over the estimated fair value of the
tangible net assets and intangible assets acquired was recorded to goodwill. Factors contributing to the recognition of the
preliminary amount of goodwill were primarily based on anticipated strategic and synergistic benefits that are expected to be
realized from the Bolder acquisition. These benefits include expanding the Company's surgical portfolio and utilizing GYN
Surgical's sales and regulatory expertise to drive adoption and revenue growth. None of the goodwill is expected to be
deductible for income tax purposes.
Fiscal 2021 Acquisitions
Mobidiag
On June 17, 2021, the Company completed the acquisition of Mobidiag Oy ("Mobidiag"), for a purchase price of
$729.6 million. Mobidiag, located in Finland, manufactures molecular diagnostic solutions for gastrointestinal infections,
antimicrobial resistance management and other infections. Mobidiag's results of operations are reported in the Company's
Diagnostics reportable segment from the date of acquisition.
The total purchase price was allocated to Mobidiag's tangible and identifiable intangible assets and liabilities based on the
estimated fair values as of June 17, 2021, as set forth below.
Cash
Accounts receivable
Inventory
Other assets
Accounts payable and accrued expenses
Other liabilities
Identifiable intangible assets:
Developed technology
In-process research and development
Customer relationships
Trade names
Current debt
Deferred income taxes, net
Goodwill
Purchase Price
$
$
7.0
4.2
12.1
29.6
(16.5)
(12.2)
285.0
74.0
20.9
20.0
(66.1)
(56.1)
427.7
729.6
In performing the purchase price allocation, the Company considered, among other factors, the intended future use of
acquired assets, analysis of historical financial performance and estimates of future performance of Mobidiag's business.
As part of the purchase price allocation, the Company determined the identifiable intangible assets are development
technology, in-process research and development ("IPR&D"), customer relationships and trade names. The fair value of the
intangible assets was estimated using the income approach, and the cash flow projections were discounted using rates ranging
from 15.0% to 19.0%. The cash flows were based on estimates used to price the transaction, and the discount rates applied were
benchmarked with reference to the implied rate of return from the transaction model and the weighted average cost of capital.
The developed technology assets are comprised of know-how, patents and technologies embedded in Mobidiag's products
and relate to currently marketed products. The developed technology assets comprise the primary product families under the
Novodiag and Amplidiag technology platforms.
The IPR&D project relates to an in-process project that had not reached technological feasibility as of the acquisition date
and has no alternative future use. The primary basis for determining technological feasibility of the project is obtaining
regulatory approval to market the underlying product. The asset recorded relates to one project, and the Company expects to
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complete the project in approximately three years. In the fourth quarter of fiscal 2022 in connection with the annual impairment
test for indefinite-lived intangible assets the Company recorded an impairment charge of $27.7 million to record the asset at fair
value. The reduction in fair value was due to an increase in the discount rate from higher interest rates, a reduction in forecasted
revenues and timing of completing the project. Given the uncertainties inherent with product development and introduction,
there can be no assurance that the Company's product development efforts will be successful, completed on a timely basis or
within budget, if at all. The IPR&D asset was valued using the income approach.
The weighted average life for the developed technology assets was 11.7 years, for customer relationships was 9.1 years,
and for tradenames was 11.6 years. The calculation of the excess of the purchase price over the estimated fair value of the
tangible net assets and intangible assets acquired was recorded to goodwill. Factors contributing to the recognition of the
amount of goodwill were primarily based on anticipated strategic and synergistic benefits that are expected to be realized from
the Mobidiag acquisition. These benefits include expanding the Company's molecular diagnostics portfolio into the near-patient
testing market and utilizing the Diagnostic's commercial sales, manufacturing and regulatory expertise to drive adoption and
revenue growth. None of the goodwill is expected to be deductible for income tax purposes.
Biotheranostics
On February 22, 2021, the Company completed the acquisition of Biotheranostics, Inc. ("Biotheranostics"), for a purchase
price of $231.3 million. Biotheranostics, located in San Diego, California, manufactures molecular diagnostic tests that support
physicians in the treatment of breast cancer and all metastatic cancers and performs the lab testing procedures at its Clinical
Laboratory Improvement Amendments ("CLIA") certified laboratory. Biotheranostics' results of operations are reported in the
Company's Diagnostics reportable segment from the date of acquisition and its revenues are reported within Service and other
revenue in the Company's Consolidated Statement of Income and within service revenue in the disclosure of disaggregated
revenue in Note 3.
The total purchase price was allocated to Biotheranostics' tangible and identifiable intangible assets and liabilities based
on the estimated fair values as of February 22, 2021, as set forth below.
Cash
Accounts receivable
Other assets
Accounts payable and accrued expenses
Other liabilities
Identifiable intangible assets:
Developed technology
Trade names
Deferred income taxes, net
Goodwill
Purchase Price
$
$
9.6
6.6
6.5
(8.2)
(8.1)
160.3
2.1
(18.4)
80.9
231.3
In performing the purchase price allocation, the Company considered, among other factors, the intended future use of
acquired assets, analysis of historical financial performance and estimates of future performance of Biotheranostics' business.
As part of the purchase price allocation, the Company determined the identifiable intangible assets are developed technology
and trade names. The fair value of the intangible assets was estimated using the income approach, and the cash flow projections
were discounted using a 18.0% rate. The cash flows were based on estimates used to price the transaction, and the discount rate
applied was benchmarked with reference to the implied rate of return from the transaction model and the weighted average cost
of capital. The weighted average life of developed technology and trade names was 10 years. The calculation of the excess of
the purchase price over the estimated fair value of the tangible net assets and intangible assets acquired was recorded to
goodwill. Factors contributing to the recognition of the amount of goodwill were primarily based on anticipated synergistic
benefits of adding Biotheranostics' CLIA lab to the Company's portfolio of offerings and of utilizing Diagnostic's marketing and
regulatory expertise to drive adoption and revenue growth. None of the goodwill is expected to be deductible for income tax
purposes.
Diagenode
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On March 1, 2021, the Company completed the acquisition of Diagenode SA ("Diagenode") for a purchase price of
$155.1 million. Diagenode, located in Belgium, is a developer and manufacturer of molecular diagnostic assays based on PCR
(polymerase chain reaction) technology to detect infectious diseases of bacterial, viral or parasite origin. Diagenode's results of
operations are reported in the Company's Diagnostics reportable segment from the date of acquisition.
The total purchase price was allocated to Diagenode's tangible and identifiable intangible assets and liabilities based on
the estimated fair values as of March 1, 2021, as set forth below.
Cash
Accounts receivable
Inventory
Other assets
Accounts payable and accrued expenses
Other liabilities
Identifiable intangible assets:
Developed technology
Customer relationships
Deferred income taxes, net
Goodwill
Purchase Price
$
$
5.6
9.3
9.0
13.9
(16.7)
(9.2)
69.8
9.2
(19.3)
83.5
155.1
In performing the purchase price allocation, the Company considered, among other factors, the intended future use of
acquired assets, analysis of historical financial performance and estimates of future performance of Diagenode's business. As
part of the purchase price allocation, the Company determined the identifiable intangible assets are developed technology and
customer relationships. The fair value of the intangible assets was estimated using the income approach, and the cash flow
projections were discounted using a 14.5% rate for developed technology and a 13.5% rate for customer relationships. The cash
flows were based on estimates used to price the transaction, and the discount rate applied were benchmarked with reference to
the implied rate of return from the transaction model and the weighted average cost of capital. The weighted average life of
developed technology and customer relationships was 10 years. The calculation of the excess of the purchase price over the
estimated fair value of the tangible net assets and intangible assets acquired was recorded to goodwill. Factors contributing to
the recognition of the amount of goodwill were based on anticipated synergistic benefits of Diagenode's products broadening
the Diagnostics portfolio of molecular diagnostics products primarily in the transplant and acute care gastrointestinal and
respiratory space as customers seek a broader menu of tests, utilizing Diagnostic's sales force to drive menu expansion and
revenue growth and gaining additional PCR assay development expertise. None of the goodwill is expected to be deductible for
income tax purposes.
Somatex Medical Technologies
On December 30, 2020, the Company completed the acquisition of Somatex Medical Technologies GmbH ("Somatex")
for a purchase price of $62.9 million. Somatex, located in Germany, is a manufacturer of biopsy site markers, including the
Tumark product line of tissue markers, which were distributed by the Company in the U.S. prior to the acquisition. The
allocation of the purchase price was based on the Company's valuation, and it allocated $38.0 million to the value of developed
technology with a weighted average life of 8 years, $1.2 million to customer relationships, $0.9 million to trade names and
$32.4 million to goodwill. The remaining $9.6 million of the purchase price was allocated to the net acquired tangible assets
and liabilities. Somatex' results of operations are reported in the Company's Breast Health reportable segment from the date of
acquisition. None of the goodwill is expected to be deductible for income tax purposes.
NXC Imaging
On September 28, 2020, the Company completed the acquisition of assets from NXC Imaging for a purchase price of
$5.6 million. NXC Imaging was a long-standing distributor of the Company's Breast and Skeletal Health products in the U.S.
The majority of the purchase price was allocated to a customer relationships intangible asset with a useful life of 5 years.
Fiscal 2020 Acquisitions
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Acessa Health
On August 23, 2020, the Company completed the acquisition of Acessa Health, Inc. ("Acessa") for a purchase price of
$162.0 million, which included a hold-back of $3.0 million that was paid in January 2021, and contingent consideration, which
the Company estimated the fair value to be $81.8 million as of the measurement date. Acessa, located in Austin, Texas,
manufactures and markets the ProVu system, a laparoscopic radio frequency ablation system for use in treatment of uterine
fibroids. Acessa's results of operations are reported in the Company's GYN Surgical reportable segment from the date of
acquisition.
The contingent payments are based on a multiple of annual incremental revenue growth over a three-year period ending
annually in December of each 2021, 2022, and 2023. There is no maximum earnout. Pursuant to ASC 805, Business
Combinations (ASC 805), the Company recorded its estimate of the fair value of the contingent consideration liability utilizing
the Monte Carlo simulation based on future revenue projections of Acessa, revenue growth rates of comparable companies,
implied volatility and applying a risk adjusted discount rate. Each quarter the Company is required to remeasure the fair value
of the liability as assumptions change and such adjustments are recorded in operating expenses. This fair value measurement
was based on significant inputs not observable in the market and thus represented a Level 3 measurement as defined in ASC
820, Fair Value Measurements. This fair value measurement is directly impacted by the Company's estimate of future
incremental revenue growth of the business. Accordingly, if actual revenue growth is higher or lower than the estimates within
the fair value measurement, the Company would record additional charges or gains. During the year ended September 24, 2022,
the Company remeasured the contingent consideration and recorded a gain of $39.5 million to record the liability at fair value.
The reduction in fair value was primarily due to a decrease in forecasted revenues over the measurement period and to a much
lesser extent an increase in the discount rate driven by market rates. During the year ended September 25, 2021, the Company
remeasured the contingent consideration liability and recorded a gain of $6.7 million to record the liability at fair value. The
reduction in fair value was primarily due to a decrease in forecasted revenues over the measurement period, partially offset by a
lower discount rate and accretion of the liability based on the passage of time. During the second quarter of fiscal 2022, the
Company made a payment of $12.2 million for the first earn-out period. As of September 24, 2022, the contingent
consideration liability was $23.4 million, $12.0 million of which was recorded within accrued expenses and $11.4 million was
recorded within other long-term liabilities.
The total purchase price was allocated to Acessa's tangible and identifiable intangible assets and liabilities based on the
estimated fair values as of August 23, 2020, as set forth below.
Cash
Inventory
Other assets
Accounts payable and accrued expenses
Identifiable intangible assets:
Developed Technology
Trade names
Deferred income taxes, net
Goodwill
Purchase Price
$
$
1.2
4.0
4.4
(4.7)
127.0
1.2
(20.2)
49.1
162.0
In performing the purchase price allocation, the Company considered, among other factors, the intended future use of
acquired assets, analysis of historical financial performance and estimates of future performance of Acessa's business. As part
of the purchase price allocation, the Company determined the identifiable intangible assets were developed technology and
trade names. The fair value of the intangible assets was estimated using the income approach, and the cash flow projections
were discounted using an 18.0% rate. The cash flows were based on estimates used to price the transaction, and the discount
rate applied was benchmarked with reference to the implied rate of return from the transaction model and the weighted average
cost of capital. The weighted average life of developed technology and trade names is 10 years. The calculation of the excess of
the purchase price over the estimated fair value of the tangible net assets and intangible assets acquired was recorded to
goodwill. Factors contributing to the recognition of the amount of goodwill were based on synergistic benefits of Acessa's
products being complementary to the GYN Surgical portfolio of products and utilizing the GYN Surgical sales force to drive
adoption and revenue growth. None of the goodwill is expected to be deductible for income tax purposes.
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Health Beacons
On February 3, 2020, the Company completed the acquisition of Health Beacons, Inc. ("Health Beacons") for a purchase
price of $19.7 million. Health Beacons manufactures the LOCalizer product. Based on the Company's valuation, it allocated
$10.7 million to developed technology and $6.2 million to goodwill. The remaining $2.8 million of the purchase price was
allocated to acquired tangible assets and liabilities. Health Beacons' results of operations are reported in the Company's Breast
Health reportable segment from the date of acquisition.
Alpha Imaging
On December 30, 2019, the Company completed the acquisition of assets from Alpha Imaging, LLC ("Alpha Imaging")
for a purchase price of $18.0 million. Alpha Imaging was a long-standing distributor of the Company's Breast and Skeletal
Health products in the U.S. The majority of the purchase price was allocated to a customer relationships intangible asset with a
useful life of 5 years.
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6. Restructuring and Divestiture Charges
The Company evaluates its operations for opportunities to improve operational effectiveness and efficiency, including
facility and operations consolidation, and to better align expenses with revenues. As a result of these assessments, the Company
has undertaken various restructuring actions which are described below. The following table displays charges taken related to
restructuring actions in fiscal 2022, 2021 and 2020 and a rollforward of the charges to the accrued balances as of September 24,
2022:
Fiscal 2022
Actions
Fiscal 2021
Actions
Fiscal 2020
Actions
Other
Total
Restructuring Charges
Fiscal 2020 charges:
Workforce reductions
Facility closure costs
Fiscal 2020 restructuring charges
Fiscal 2021 charges:
Workforce reductions
Fiscal 2021 restructuring charges
Fiscal 2022 charges:
Workforce reductions
Facility closure costs
Fiscal 2022 restructuring charges
Rollforward of Accrued Restructuring
Balance as of September 28, 2019
Fiscal 2020 restructuring charges
Stock-based compensation
Severance payments and adjustments
Other payments and adjustments (1)
Balance as of September 26, 2020
Fiscal 2021 restructuring charges
Stock-based compensation
Severance payments and adjustments
Balance as of September 25, 2021
Fiscal 2022 restructuring charges
Severance payments and adjustments
Balance as of September 24, 2022
$
$
$
$
$
$
$
$
$
$
$
$
$
— $
—
— $
— $
— $
2.6 $
0.5
3.1 $
—
—
—
8.7
8.7
$
$
$
$
13.2
$
1.9
15.1
$
0.6
0.6
$
(0.3) $
(0.4) $
—
—
(0.3) $
(0.4) $
0.2 $
—
0.2 $
$
— $
— $
—
— $
13.4
1.9
15.3
9.3
9.3
1.9
0.5
2.4
Fiscal 2022
Actions
Fiscal 2021
Actions
Fiscal 2020
Actions
Previous
Other Charges
Total
— $
— $
— $
5.9 $
5.9
— $
— $
15.1 $
0.2 $
—
—
—
—
—
—
(7.5)
(4.4)
0.5
—
(1.5)
(3.8)
— $
— $
3.7 $
0.8 $
— $
8.7 $
0.6 $
— $
—
—
(0.9)
(4.6)
—
(3.4)
—
(0.8)
— $
3.2 $
0.9 $
— $
3.1 $
(0.4)
2.7 $
(0.3) $
(2.5)
0.4 $
(0.4) $
(0.5)
— $
— $
—
— $
15.3
(7.5)
(5.9)
(3.3)
4.5
9.3
(0.9)
(8.8)
4.1
2.4
(3.4)
3.1
(1) In fiscal 2020, as part of the adoption of ASC 842, the Company reclassified $3.8 million from a lease liability to offset the right of use
asset on the Company's consolidated balance sheet.
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Table of Contents
Fiscal 2022 Actions
During the first quarter of fiscal 2022, the Company finalized its decision to close its Danbury, Connecticut facility
where it manufactures its Breast Health capital equipment products. The manufacturing of the Breast Health capital equipment
products and all other support services will be moved to the Company's Newark, Delaware facility. In addition, research and
development, sales and services support and administrative functions will be moved to the Newark, Delaware and
Marlborough, Massachusetts facilities. The transition is expected to be completed by the third quarter of fiscal 2025. The
majority of employees located in Danbury were given the option to relocate to the new locations. As a result of this plan, the
Company expects a number of employees to not relocate resulting in their termination. The employees were notified of the
closure during the first quarter of fiscal 2022, but were not communicated about their termination and related severance and
benefits until the third quarter of fiscal 2022. The Company is recording severance benefits pursuant to pursuant to ASC 420,
Exit or Disposal Cost Obligations (ASC 420) and the benefits will be expensed ratably over the required service period. As a
result, the Company recorded $1.6 million of severance and benefits charges in fiscal 2022. The Company estimates that total
severance and benefits charges, including retention, will be approximately $7.0 million.
During fiscal 2022, the Company made various other decisions to terminate certain individuals across multiple divisions,
outsource one of its U.S. distribution locations and consolidate its German office locations. The Company recorded $0.3 million
for severance and benefits and $0.5 million in property closure costs related to these actions, which occurred in the U.S. and
various
to ASC 712, Compensation-Nonretirement
Postemployment Benefits, (ASC 712) or ASC 420, depending on the employee and country location. The Company expects the
total charges from these actions to be approximately $3.5 million.
locations. The charges were recorded pursuant
international
Fiscal 2021 Actions
During fiscal 2021, the Company made various decisions to terminate certain individuals across all divisions in multiple
departments and close certain manufacturing facilities for minor product lines. The Company recorded $8.7 million for
severance and benefits related to these actions, which occurred in the U.S. and various international locations. The charges were
recorded pursuant to ASC 712 or ASC 420, depending on the employee and country location. These actions were completed.
Fiscal 2020 Actions
During fiscal 2020, the Company made various decisions to terminate certain personnel across all divisions in multiple
departments, transfer production and close certain manufacturing facilities for minor product lines. The Company recorded
charges totaling $13.4 million for severance and benefits related to these actions. The charges were recorded pursuant to ASC
712 or ASC 420, depending on the employee and country location. Included within this charge was $5.0 million related to the
modification of equity awards for a certain executive. These actions were completed.
During the second quarter of fiscal 2020, the Company recorded net divestiture charges of $1.9 million. The charge
included $1.3 million to dispose of the Company's life sciences testing business located in the UK, which performed research
testing for pharmaceutical companies. Separately, in connection with the Cynosure divestiture, the Company accelerated stock
compensation expense and other benefits of $2.6 million, partially offset by other adjustments of $2.0 million.
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Table of Contents
7. Borrowings and Credit Agreements
The Company’s borrowings consisted of the following:
Current debt obligations, net of debt discount and deferred issuance costs:
Term Loan
Securitization Program
Other
Total current debt obligations
Long-term debt obligations, net of debt discount and issuance costs:
Term Loan
2028 Senior Notes
2029 Senior Notes
Total long-term debt obligations
Total debt obligations
September 24,
2022
September 25,
2021
$
$
$
15.0 $
—
—
15.0 $
1,475.7
396.1
936.6
2,808.4
2,823.4 $
—
248.5
64.5
313.0
1,382.3
395.4
934.5
2,712.2
3,025.2
The debt maturity schedule for the Company’s obligations as of September 24, 2022 was as follows:
Term Loan
2028 Senior Notes
2029 Senior Notes
2023
2024
2025
$
$
15.0 $
—
—
15.0 $
37.5 $
—
—
37.5 $
37.5 $
—
—
37.5 $
2026
1,410.0 $
—
—
1,410.0 $
2027
2028 and
Thereafter
— $
—
—
— $
— $
400.0
950.0
1,350.0 $
Total
1,500.0
400.0
950.0
2,850.0
2021 Credit Agreement
On September 27, 2021, the Company and certain of its subsidiaries refinanced its then existing term loan and revolving
credit facility with Bank of America, N.A. in its capacity as Administrative Agent, Swing Line Lender and L/C Issuer, and
certain other lenders (the "2018 Credit Agreement") by entering into Refinancing Amendment No. 2 dated as of September 27,
2021, to the Amended and Restated Credit and Guaranty Agreement as of October 3, 2017, as amended (the "2021 Credit
Agreement") Borrowings under the 2021 Credit Agreement are secured by first-priority liens on, and a first-priority security
interest in, substantially all of the Company's U.S. assets and the assets of the Subsidiary Guarantors. These liens are subject to
release during the term of the facilities if the Company is able to achieve certain corporate or corporate family ratings and other
conditions are met. The credit facilities under the 2021 Credit Agreement (the "2021 Credit Facilities") consist of:
•
•
A $1.5 billion secured term loan ("2021 Term Loan") with a maturity date of September 25, 2026; and
A secured revolving credit facility ("2021 Revolver") under which the Company may borrow up to $2.0 billion,
subject to certain sublimits, with a maturity date of September 25, 2026.
On August 22, 2022, the Company and its subsidiaries amended the 2021 Credit Agreement by entering into an
amendment (the "Third Amendment") related to the planned phase out of LIBOR by the UK Financial Conduct Authority. The
interest rate applicable to the loans under the 2021 Credit Agreement, after giving effect to the Third Amendment, denominated
in U.S. Dollars were converted to a variant of the secured overnight financing rate (“SOFR”), as established from time to time
by the Federal Reserve Bank of New York, plus a corresponding spread. The Third Amendment converted the Eurocurrency
Rate to Term SOFR plus the SOFR Adjustment of 0.10% and the LIBOR Daily Floating Rate to Daily SOFR Rate plus the
SOFR Adjustment of 0.10%, effective September 23, 2022.
After giving effect to the Third Amendment, borrowings under the 2021 Credit Agreement, other than Swing Line
Loans, bear interest, at the Company's option, at the Base Rate, at the Term SOFR Rate, at the Alternative Currency Daily Rate,
or at the Daily SOFR Rate, in each case plus the Applicable Rate (as such terms are defined in the 2021 Credit Agreement).
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The Applicable Rate in regards to the Base Rate, the Term SOFR Rate, the Alternative Currency Daily Rate, the
Alternative Currency Term Rate, and the Daily SOFR Rate is subject to change depending on the Total Net Leverage Ratio (as
defined in the 2021 Credit Agreement). The borrowings of the Term Loan under the 2021 Credit Facilities, after giving effect to
the Third Amendment, initially bear interest at an annual rate equal to the Term SOFR Rate plus the SOFR Adjustment of
0.10% for a one month interest period plus an Applicable Rate equal to 1.00%. As of September 24, 2022, the interest rate
under the 2021 Term Loan was 4.18% per annum.
The Company is also required to pay a quarterly commitment fee calculated on daily basis equal to the Applicable Rate
as of such day multiplied by the undrawn committed amount available under the 2021 Revolver (taking into account any
outstanding amounts under the LC Sublimit). As of September 24, 2022, this commitment fee was 0.15% per annum for the
2021 Revolver.
The Company is required to make scheduled principal payments under the 2021 Term Loan in increasing amounts
ranging from $3.75 million per three-month period commencing with the three-month period ending on December 29, 2022 to
$18.75 million per three-month period commencing with the three month period ending on December 26, 2025. The remaining
balance of $1.335 billion (or such lesser aggregate principal amount of the Term Loans then outstanding) on the 2021 Term
Loan and any amounts outstanding under the 2021 Revolver are due at maturity. In addition, subject to the terms and conditions
set forth in the 2021 Credit Agreement, the Company is required to make certain mandatory prepayments from the net proceeds
of specified types of asset sales (subject to certain reinvestment rights), debt issuances (excluding permitted debt) and insurance
recoveries (subject to certain reinvestment rights). Certain of the mandatory prepayments are subject to reduction or elimination
if certain financial covenants are met. These mandatory prepayments are required to be applied by the Company first to the
2021 Term Loan, second to any outstanding amount under any Swing Line Loans, third to the 2021 Revolver, fourth to prepay
any outstanding reimbursement obligations with respect to letters of credit and fifth to cash collateralize such letters of credit.
Subject to certain limitations, the Company may voluntarily prepay any of the 2021 Credit Facilities without premium or
penalty. As of September 24, 2022, the outstanding principal balance of the 2021 Term Loan was $1.5 billion, and there were
no amounts outstanding under the 2021 Revolver.
The 2021 Credit Agreement contains affirmative and negative covenants customarily applicable to senior secured credit
facilities, including covenants restricting the ability of the Company, subject to negotiated exceptions, to incur additional
indebtedness and grant additional liens on its assets, engage in mergers or acquisitions or dispose of assets, enter into sale-
leaseback transactions, pay dividends or make other distributions, voluntarily prepay other indebtedness, enter into transactions
with affiliated persons, make investments, and change the nature of their businesses. In addition, the 2021 Credit Agreement
requires the Borrowers to maintain certain financial ratios. The 2021 Credit Agreement also contains customary representations
and warranties and events of default, including payment defaults, breach of representations and warranties, covenant defaults,
cross defaults and an event of default upon a change of control of the Company.
The Company evaluated the 2021 Credit Agreement for derivatives pursuant to ASC 815, Derivatives and Hedging, and
identified embedded derivatives that required bifurcation as the features are not clearly and closely related to the host
instrument. The embedded derivatives were a default provision, which could require additional interest payments, and a
provision requiring contingent payments to compensate the lenders for changes in tax deductions. The Company determined
that the fair value of these embedded derivatives was immaterial as of September 24, 2022.
Pursuant to ASC 470, Debt (ASC 470), the accounting for the refinancing was evaluated on a creditor-by-creditor basis
to determine whether each transaction should be accounted for as a modification or extinguishment. Certain creditors under the
2018 Credit Agreement did not participate in this refinancing transaction and ceased being creditors of the Company. As a
result, the Company recorded a debt extinguishment loss of $0.7 million in the first quarter of fiscal 2022 to write-off the pro-
rata amount of unamortized debt discount and deferred issuance costs related to these creditors. For the remainder of the
creditors, this transaction was accounted for as a modification. Pursuant to ASC 470, third-party costs of $7.0 million were
recorded as a reduction to debt representing deferred issuance costs and fees paid directly to the lenders.
2018 Amended and Restated Credit Agreement
On December 17, 2018, the Company and certain of its subsidiaries refinanced its term loan and revolving credit facility
by entering into an Amended and Restated Credit and Guaranty Agreement as of December 17, 2018 (the "2018 Credit
Agreement") with Bank of America, N.A. in its capacity as Administrative Agent, Swing Line Lender and L/C Issuer, and
certain other lenders. The 2018 Credit Agreement amended the Company's Amended and Restated Credit and Guaranty
Agreement dated as of October 3, 2017 ("2017 Credit Agreement").
The credit facilities under the 2018 Credit Agreement consisted of:
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Table of Contents
•
•
A $1.5 billion secured term loan ("2018 Term Loan") with a maturity date of December 17, 2023; and
A secured revolving credit facility ("2018 Revolver") under which the Company could borrow up to $1.5 billion,
subject to certain sublimits, with a maturity date of December 17, 2023.
Borrowings under the 2018 Credit Agreement bore interest, at the Company's option and in each case plus an applicable
margin as follows:
•
•
2018 Term Loan: at the Base Rate, Eurocurrency Rate or LIBOR Daily Floating Rate,
2018 Revolver: if funded in U.S. dollars, the Base Rate, Eurocurrency Rate, or LIBOR Daily Floating Rate, and, if
funded in an alternative currency, the Eurocurrency Rate; and if requested under the swing line sublimit, the Base
Rate.
Interest expense, non-cash interest expense, the weighted average interest rate, and the interest rate at the end of period
under the 2021 Credit Agreement and the 2018 Credit Agreement were as follows:
Interest expense (1)
Non-cash interest expense
Weighted average interest rate
Interest rate at end of period
Years Ended
September 24, 2022
September 25, 2021
September 26, 2020
$
$
31.8
2.2
$
$
1.74 %
4.18 %
22.0
2.5
$
$
1.13 %
1.08 %
46.6
2.5
2.25 %
1.40 %
(1) Interest expense includes non-cash interest expense related to the amortization of the deferred issuance costs and
accretion of the debt discount.
Senior Notes
2028 Senior Notes
On January 19, 2018, the Company completed a private placement of $1.0 billion aggregate principal amount of senior
notes and allocated $400 million in aggregate principal amount to its 4.625% Senior Notes due 2028 (the "2028 Senior Notes")
at an offering price of 100% of the aggregate principal amount of the 2028 Senior Notes. The 2028 Senior Notes are general
senior unsecured obligations of the Company and are guaranteed on a senior unsecured basis by certain domestic subsidiaries.
The 2028 Senior Notes mature on February 1, 2028 and bear interest at the rate of 4.625% per year, payable semi-annually on
February 1 and August 1 of each year, commencing on August 1, 2018.
The Company may redeem the 2028 Senior Notes at any time prior to February 1, 2023 at a price equal to 100% of the
aggregate principal amount so redeemed, plus accrued and unpaid interest, if any, to the redemption date and a make-whole
premium set forth in the indenture. The Company has the option to redeem the 2028 Senior Notes on or after: February 1, 2023
through February 1, 2024 at 102.312% of par; February 1, 2024 through February 1, 2025 at 101.541% of par; February 1, 2025
through February 1, 2026 at 100.770% of par; and February 1, 2026 and thereafter at 100% of par. In addition, if the Company
undergoes a change of control coupled with a decline in ratings, as provided in the indenture, the Company will be required to
make an offer to purchase each holder’s 2028 Senior Notes at a price equal to 101% of their principal amount, plus accrued and
unpaid interest, if any, to the repurchase date.
The Company evaluated the 2028 Senior Notes for derivatives pursuant to ASC 815 and did not identify any embedded
derivatives that require bifurcation. All features were deemed to be clearly and closely related to the host instrument.
2029 Senior Notes
On September 28, 2020, the Company completed a private placement of $950 million aggregate principal amount of its
3.250% Senior Notes due 2029 (the "2029 Senior Notes") at an offering price of 100% of the aggregate principal amount of the
2029 Senior Notes. The 2029 Senior Notes are general senior unsecured obligations of the Company and are guaranteed on a
senior unsecured basis by certain domestic subsidiaries. The 2029 Senior Notes mature on February 15, 2029 and bear interest
at the rate of 3.250% per year, payable semi-annually on February 15 and August 15 of each year, commencing on February 15,
2021.
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The Company may redeem the 2029 Senior Notes at any time prior to September 28, 2023 at a price equal to 100% of the
aggregate principal amount so redeemed, plus accrued and unpaid interest, if any, to the redemption date and a make-whole
premium set forth in the indenture. The Company may also redeem up to 40% of the aggregate principal amount of the 2029
Senior Notes with the net cash proceeds of certain equity offerings at any time and from time to time before September 28,
2023, at a redemption price equal to 103.250% of the aggregate principal amount so redeemed, plus accrued and unpaid
interest, if any, to the redemption date. The Company also has the option to redeem the 2029 Senior Notes on or after:
September 28, 2023 through September 27, 2024 at 101.625% of par; September 28, 2024 through September 27, 2025 at
100.813% of par; and September 28, 2025 and thereafter at 100% of par. In addition, if the Company undergoes a change of
control coupled with a decline in ratings, as provided in the indenture, the Company will be required to make an offer to
purchase each holder’s 2029 Senior Notes at a price equal to 101% of their principal amount, plus accrued and unpaid interest,
if any, to the repurchase date.
The Company evaluated the 2029 Senior Notes for derivatives pursuant to ASC 815, Derivatives and Hedging, and did
not identify any embedded derivatives that require bifurcation. All features were deemed to be clearly and closely related to the
host instrument.
2025 Senior Notes
The Company had 4.375% Senior Notes due 2025 (the “2025 Senior Notes”) outstanding and bore interest at the rate of
4.375% per year, payable semi-annually on April 15 and October 15 of each year. The Company used the net proceeds of the
2029 Senior Notes offering in the first quarter of fiscal 2021 to redeem in full the 2025 Senior Notes in the aggregate principal
amount of $950.0 million on October 15, 2020 at an aggregate redemption price of $970.8 million, which included a premium
payment of $20.8 million. Since the Company planned to use the proceeds from the 2029 Senior Notes offering to redeem the
2025 Senior Notes, the Company evaluated the accounting for this transaction under ASC 470 to determine modification versus
extinguishment accounting on a creditor-by-creditor basis. Certain 2025 Senior Note holders either did not participate in this
refinancing transaction or reduced their holdings and these transactions were accounted for as extinguishments. As a result, the
Company recorded a debt extinguishment loss in the first quarter of fiscal 2021 of $21.6 million, which comprised pro-rata
amounts of the premium payment, debt discount and debt issuance costs. For the remaining 2025 Senior Notes holders who
participated in the refinancing, these transactions were accounted for as a modification because on a creditor-by-creditor basis
the present value of the cash flows between the debt instruments before and after the transaction was less than 10%. The
Company recorded a portion of the transaction expenses of $5.8 million to interest expense pursuant to ASC 470, subtopic
50-40. The remaining debt issuance costs of $7.9 million and debt discount of $6.4 million related to the modified debt are
being amortized over the new term of the 2029 Senior Notes using the effective interest method.
Interest expense for the 2029 Senior Notes, 2028 Senior Notes and 2025 Senior Notes was as follows:
September 24, 2022
September 25, 2021
September 26, 2020
Years Ended
2029 Senior Notes
2028 Senior Notes
2025 Senior Notes
Total
Interest
Rate
Interest
Expense (1)
3.250 % $
4.625 %
4.375 %
32.9 $
19.2
—
Non-Cash
Interest
Expense
Interest
Expense (1)
Non-Cash
Interest
Expense
Interest
Expense (1)
Non-Cash
Interest
Expense
2.1 $
0.7
—
32.7 $
19.2
2.3
2.1 $
0.7
0.1
— $
19.2
43.5
62.7 $
—
0.7
2.1
2.8
$
52.1 $
2.8 $
54.2 $
2.9 $
(1) Interest expense includes non-cash interest expense related to the amortization of the deferred issuance costs and
accretion of the debt discount.
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Accounts Receivable Securitization Program
On April 25, 2016, the Company entered into a one-year $200.0 million accounts receivable securitization program (the
"Securitization Program") with several of its wholly owned subsidiaries and certain financial institutions, which provides for
annual renewals. Under the terms of the Securitization Program, the Company and certain of its wholly-owned subsidiaries sell
their respective customer receivables to a bankruptcy remote special purpose entity, which is also a wholly-owned subsidiary of
the Company. In addition, the Company also contributed a portion of its customer receivables to the special purpose entity in
connection with its establishment. The Company retains servicing responsibility. The special purpose entity, as borrower, and
the Company, as servicer, entered into a Credit and Security Agreement with several lenders pursuant to which the special
purpose entity, at that time, could borrow up to $200.0 million from the lenders, with the loans secured by the receivables. The
amount that the special purpose entity may borrow at a given point in time is determined based on the amount of qualifying
receivables that are present in the special purpose entity at such point in time. Borrowings outstanding under the Securitization
Program bore interest at LIBOR plus the applicable margin of 0.8% and were included as a component of current liabilities in
the Company's consolidated balance sheet, while the accounts receivable securing these obligations remain as a component of
net receivables in the Company's consolidated balance sheet. The Company and the special purpose entity are operated and
maintained as separate legal entities. The assets of the special purpose entity secure the amounts borrowed and cannot be used
to pay other debts or liabilities of the Company. In subsequent years, the Company amended the agreement to extend it for one-
year periods and increased the borrowing capacity up to $250.0 million and lowered the applicable margin to 0.7%.
On June 11, 2021, the Company amended and restated the Credit and Security Agreement and increased the maximum
borrowing amount to $320.0 million. During fiscal 2022, the Company repaid the outstanding balance of $248.5 million under
the accounts receivable securitization program. On June 10, 2022, the Company amended the Credit and Security agreement
and temporarily suspended the ability to borrow and the need to comply with covenants for up to a year. As of September 24,
2022, the Company did not have any borrowings under the program.
Borrowings under the Securitization Program for fiscal 2022, through the second quarter of fiscal 2022, had a weighted-
average interest rate of 0.81%. Interest expense under the Securitization Program was $1.6 million, $0.9 million and $3.1
million for fiscal 2022, 2021 and 2020, respectively.
The Credit and Security Agreement contains customary representations and warranties and events of default, including
payment defaults, breach of representations and warranties, covenant defaults, and an event of default upon a change of control
of the Company. In addition, it contains financial covenants consistent with that of the Credit Agreement. As of September 24,
2022, the Company was not required to be in compliance with the Credit and Security Agreement covenants.
Other
Other represents debt acquired in the Mobidiag acquisition, which was primarily with the European Investment Bank
("EIB"). Mobidiag had withdrawn multiple tranches under the agreement, which were primarily used to fund research and
development projects and expansion efforts. The debt agreement contained change-in-control provisions allowing the EIB to
call the debt at any time after a change-in-control, which occurred as a result of Hologic acquiring Mobidiag. The tranches
withdrawn under this agreement had interest rates ranging from 6.0% to 7.0%. The debt agreement included additional
payments to the EIB based on revenues generated by products developed under the funding as well as prepayment penalties.
During the first quarter of fiscal 2022, the Company paid off the outstanding debt obligation of $63.7 million, and the debt
agreement with the EIB was terminated.
8. Fair Value Measurements
The Company applies the provisions of ASC 820 for its financial assets and liabilities that are re-measured and reported
at fair value each reporting period and its nonfinancial assets and liabilities that are re-measured and reported at fair value on a
non-recurring basis. Fair value is the price that would be received from selling an asset or paid to transfer a liability in an
orderly transaction between market participants at the measurement date. When determining fair value, the Company considers
the principal or most advantageous market in which it would transact and considers assumptions that market participants would
use when pricing the asset or liability.
Fair Value Hierarchy
ASC 820 establishes a three-level valuation hierarchy for disclosure of fair value measurements. Financial assets and
liabilities are categorized within the valuation hierarchy based upon the lowest level of input that is significant to the
measurement of fair value. The three levels of the hierarchy are defined as follows:
•
Level 1—Inputs to the valuation methodology are quoted market prices for identical assets or liabilities.
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•
•
Level 2—Inputs to the valuation methodology are other observable inputs, including quoted market prices for similar
assets or liabilities and market-corroborated inputs.
Level 3—Inputs to the valuation methodology are unobservable inputs based on management’s best estimate of inputs
market participants would use in pricing the asset or liability at the measurement date, including assumptions about risk.
Assets/Liabilities Measured and Recorded at Fair Value on a Recurring Basis
The Company has investments in derivative instruments comprised of an interest rate swap, forward foreign currency
contracts and foreign currency option contracts, which are valued using analyses obtained from independent third-party
valuation specialists based on market observable inputs, representing Level 2 assets. The fair values of these derivative
contracts represent the estimated amounts the Company would receive or pay to terminate the contracts. Refer to Note 2 for
further discussion and information on these derivative contracts. In addition, the Company has contingent consideration
liabilities that are recorded at fair value and are based on Level 3 inputs. The contingent consideration liability as of
September 24, 2022 and September 25, 2021 was related to the Acessa acquisition (see Note 5).
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Assets and liabilities measured and recorded at fair value on a recurring basis consisted of the following:
Assets:
Interest rate swap
Forward foreign currency contracts
Total
Liabilities:
Contingent consideration
Total
Assets:
Forward foreign currency contracts
Total
Liabilities:
Contingent consideration
Interest rate swap
Forward foreign currency contracts
Total
Fair Value Measurements at September 24, 2022
Quoted Prices in
Active Market for
Identical Assets
(Level 1)
Significant
Other
Observable
Inputs (Level 2)
Significant
Unobservable
Inputs (Level 3)
Carrying Value
$
$
$
$
38.9 $
26.4
65.3 $
23.4 $
23.4 $
— $
—
— $
— $
— $
38.9 $
26.4
65.3 $
— $
— $
—
—
—
23.4
23.4
Fair Value Measurements at September 25, 2021
Quoted Prices in
Active Market for
Identical Assets
(Level 1)
Significant
Other
Observable
Inputs (Level 2)
Significant
Unobservable
Inputs (Level 3)
Carrying Value
$
$
$
$
1.7 $
1.7 $
75.1 $
18.7
0.6
94.4 $
— $
— $
— $
—
—
— $
1.7 $
1.7 $
— $
18.7
0.6
19.3 $
—
—
75.1
—
—
75.1
Changes in the fair value of recurring fair value measurements using significant unobservable inputs (Level 3), which
solely consisted of contingent consideration liabilities, during the years ended September 24, 2022, September 25, 2021, and
September 26, 2020 were as follows:
Balance at beginning of period
Contingent consideration recorded at acquisition
Fair value adjustments
Payments/Accruals
Balance at end of period
Years Ended
2022
2021
2020
$
$
75.1 $
—
(39.5)
(12.2)
23.4 $
81.8 $
—
(6.7)
—
75.1 $
9.1
82.7
0.3
(10.3)
81.8
Assets Measured and Recorded at Fair Value on a Nonrecurring Basis
The Company remeasures the fair value of certain assets and liabilities upon the occurrence of certain events. Such assets
are comprised of equity investments and long-lived assets, including property, plant and equipment, intangible assets and
goodwill. During the fourth quarter of fiscal 2022, the Company recorded a $27.7 million impairment charge to record an
IPR&D asset at fair value, which is a Level 3 measurement, and it recorded an $8.2 million impairment charge to write-off a
developed technology asset from its Focal acquisition. In addition, the Company recorded an impairment charge of $4.0 million
to record an equity investment at its estimated fair value. During the third quarter of fiscal 2022, the Company recorded a
$9.2 million impairment charge to write-off two developed technology assets from its Faxitron acquisition. During the second
quarter of fiscal 2022, the Company recorded a $4.3 million impairment charge to write-off an equity method investment
acquired in the Mobidiag acquisition. During the fourth quarter of fiscal 2021, the Company recorded an impairment charge of
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$1.8 million to record an equity investment to its fair value. During the first quarter of fiscal 2020, the Company's Medical
Aesthetics division met the criteria to be classified as assets-held-for sale, and the Company recorded a $30.2 million loss to
record the asset group at its fair value less costs to sell. This was a level 1 measurement. Refer to Note 6 for disclosure of the
nonrecurring fair value measurement related to the debt extinguishment losses recorded in fiscal 2022 and 2021.
Disclosure of Fair Value of Financial Instruments
The Company’s financial instruments mainly consist of cash and cash equivalents, accounts receivable, equity
investments, an interest rate swap, forward foreign currency contracts, foreign currency option contracts, insurance contracts,
accounts payable and debt obligations. The carrying amounts of the Company’s cash and cash equivalents, accounts receivable
and accounts payable approximate their fair value due to the short-term nature of these instruments. The Company’s interest
rate swap, forward foreign currency contracts and foreign currency option contracts are recorded at fair value. The carrying
amount of the insurance contracts are recorded at their cash surrender value, as required by U.S. GAAP, which approximates
fair value. The Company believes the carrying amounts of its equity investments approximate fair value.
Amounts outstanding under the Company’s 2021 Credit Agreement of $1.5 billion aggregate principal as of
September 24, 2022 are subject to variable rates of interest based on current market rates, and as such, the Company believes
the carrying amount of these obligations approximates fair value. The Company’s 2028 Senior Notes and 2029 Senior Notes
had fair values of approximately $365.7 million and $783.9 million, respectively, as of September 24, 2022 based on their
trading price, representing a Level 1 measurement. Refer to Note 7 for the carrying amounts of the various components of the
Company's debt.
9. Income Taxes
The Company’s income before income taxes consisted of the following:
Domestic
Foreign
Years ended
September 24,
2022
September 25,
2021
September 26,
2020
$
$
1,340.3 $
247.9
1,588.2 $
2,267.8 $
93.3
2,361.1 $
921.1
80.8
1,001.9
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Table of Contents
The provision (benefit) for income taxes contained the following components:
Federal:
Current
Deferred
State:
Current
Deferred
Foreign:
Current
Deferred
Years ended
September 24,
2022
September 25,
2021
September 26,
2020
$
$
298.6 $
(129.8)
168.8
54.8
(9.5)
45.3
99.0
(26.9)
72.1
286.2 $
453.6 $
(45.6)
408.0
84.7
(11.9)
72.8
23.2
(12.6)
10.6
491.4 $
(62.1)
(76.6)
(138.7)
33.9
(12.5)
21.4
14.0
(5.3)
8.7
(108.6)
The income tax provision differed from the tax provision computed at the U.S. federal statutory rate due to the following:
Income tax provision at federal statutory rate
Increase (decrease) in tax resulting from:
Cynosure loss on sale and carryback
State income taxes, net of federal benefit
U.S. tax on foreign earnings
Internal restructuring
Tax credits
Unrecognized tax benefits
Compensation
Foreign rate differential
Change in deferred tax rate
Change in valuation allowance
Other
Years ended
September 24,
2022
September 25,
2021
September 26,
2020
21.0 %
21.0 %
21.0 %
(1.2)
2.9
(2.6)
(0.9)
(0.5)
0.2
0.2
(0.8)
0.4
0.4
(1.1)
18.0 %
—
2.7
(2.7)
—
(0.3)
0.3
0.1
(0.7)
(0.3)
—
0.7
20.8 %
(31.3)
2.9
(2.6)
—
(0.6)
—
0.4
(1.2)
(0.6)
1.3
(0.1)
(10.8) %
The Company's effective tax rate for fiscal 2022 was lower than the U.S. statutory tax rate primarily due to the impact of
the U.S. deduction for foreign derived intangible income, reserve releases resulting from statute of limitations expirations and
favorable audit settlements (net of reserve additions for uncertain tax positions), the geographic mix of income earned by the
Company's international subsidiaries, which are taxed at rates lower than the U.S. statutory tax rate, and a tax benefit related to
an internal restructuring, partially offset by state income taxes and the global intangible low-taxed income inclusion.
The Company’s effective tax rate for fiscal 2021 was lower than the U.S. statutory tax rate primarily due to the impact of
the U.S. deduction for foreign derived intangible income and the geographic mix of income earned by the Company's
international subsidiaries, which are taxed at rates lower than the U.S. statutory tax rate, partially offset by state income taxes
and the global intangible low-taxed income inclusion.
The Company’s effective tax rate for fiscal 2020, which was a net benefit, differed from the U.S. statutory tax rate
primarily due to a $313.4 million net tax benefit related to the sale of the Medical Aesthetics business, the impact of the U.S.
deduction for foreign derived intangible income, federal and state tax credits, and the geographic mix of income earned by the
Company's international subsidiaries, which are taxed at rates lower than the U.S. statutory tax rate, partially offset by state
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income taxes, reserves for uncertain tax positions (net of releases resulting from statute of limitations expirations and favorable
audit settlements), the global intangible low-taxed income inclusion, and unbenefited foreign losses.
The Company uses the asset and liability method to account for income taxes in accordance with ASC 740, Accounting
for Income Taxes. Under this method, deferred income tax assets and liabilities are recognized for the future tax consequences
of differences between the financial statement carrying amount of existing assets and liabilities and their respective tax bases
and also for operating loss and tax credit carry-forwards at each reporting period. Deferred income taxes are based on enacted
tax laws and statutory tax rates applicable to the period and jurisdiction in which these differences are expected to affect taxable
income. A valuation allowance is established when necessary to reduce deferred tax assets to the amounts expected to be
realized.
The Company’s significant deferred tax assets and liabilities were as follows:
Deferred tax assets
Net operating loss carryforwards
Capital losses
Non-deductible accruals
Non-deductible reserves
Stock-based compensation
Tax credits
Nonqualified deferred compensation plan
Lease liability
Other temporary differences
Less: valuation allowance
Deferred tax liabilities
Depreciation and amortization
Right of use asset
Other temporary differences
September 24,
2022
September 25,
2021
$
$
$
$
$
91.4 $
54.3
30.1
44.6
18.8
8.9
13.2
11.8
—
273.1
(115.3)
157.8 $
(220.6) $
(11.4)
(0.4)
(232.4) $
(74.6) $
91.5
52.0
34.9
41.8
17.6
10.0
16.8
16.2
17.4
298.2
(121.3)
176.9
(389.7)
(15.8)
—
(405.5)
(228.6)
Under ASC 740, the Company can only recognize the future benefit of deferred tax assets to the extent that it is “more
likely than not” that these assets will be realized. After considering all available positive and negative evidence, the Company
established a valuation allowance against specifically identified deferred tax assets because it is more-likely-than-not that these
assets will not be realized. In making this determination, the Company considered numerous factors including historical
profitability, estimated future taxable income and the character of such income. The valuation allowance decreased $6.0 million
in fiscal 2022 from fiscal 2021 primarily due to valuation allowance releases, currency translation adjustments, and attribute
utilization and expiration, partially offset by valuation allowances recorded against loss carryforwards and to reflect the impact
of an internal restructuring on state credit carryforwards.
As of September 24, 2022, the Company had $89.3 million, $143.3 million, and $266.7 million in gross federal, state, and
foreign net operating losses, respectively, $4.3 million, $4.2 million, and $0.2 million in federal, state, and foreign credit
carryforwards, respectively, and $26.2 million, and $32.2 million in gross state and foreign capital loss carryforwards,
respectively. These losses, credits, and capital loss carryforwards expire between 2023 and 2042, except for $314.8 million in
losses, $2.4 million in credits, and $32.2 million in capital loss carryforwards that have unlimited carryforward periods. The
state and foreign net operating losses include $78.8 million, and $3.4 million, respectively, and the state capital loss
carryforwards include $26.2 million, that the Company expects will expire unutilized.
As of September 24, 2022, the Company had $247.6 million in gross unrecognized tax benefits excluding interest, of
which $231.6 million, if recognized, would reduce the Company's effective tax rate. As of September 25, 2021, the Company
had $212.8 million in gross unrecognized tax benefits excluding interest, of which $197.0 million, if recognized, would have
reduced the Company's effective tax rate. The $34.8 million increase in gross unrecognized tax benefits from fiscal 2021 was
primarily due to the effect of an internal restructuring, intercompany transfer pricing for ordinary business operations, a
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carryback claim, capital losses and other current year positions, partially offset by reserve releases resulting from statute of
limitations expirations and audit settlements. In the next twelve months it is reasonably possible that the Company will reduce
its gross unrecognized tax benefits excluding interest by up to $2.0 million due to expiring statutes of limitations.
The Company’s unrecognized income tax benefits activity for fiscal 2022 and 2021 was as follows:
Balance at beginning of fiscal year
Tax positions related to current year:
Additions
Reductions
Tax positions related to prior years:
Additions related to change in estimate
Reductions
Payments
Lapses in statutes of limitations and settlements
Acquired tax positions:
Additions related to reserves acquired from
acquisitions
Balance as of the end of the fiscal year
2022
2021
$
212.8 $
197.1
45.9
—
21.5
(6.6)
—
(26.0)
8.0
—
7.9
(0.3)
—
(1.7)
—
247.6 $
1.8
212.8
$
The Company’s policy is to include accrued interest and penalties related to unrecognized tax benefits and income tax
liabilities, when applicable, as a component of income tax expense. As of September 24, 2022, and September 25, 2021, gross
accrued interest was $14.3 million and $13.7 million, respectively, and accrued penalties were immaterial.
The Company and its subsidiaries are subject to examination by U.S. federal, state, and foreign tax authorities. The
Company is currently undergoing several income tax audits including examinations by the U.S. Internal Revenue Service (fiscal
years 2017-2020), U.K. HM Revenue and Customs (fiscal years 2016-2020) and various state tax authorities. Excluding
jurisdictions under audit, the Company’s income tax returns are generally no longer subject to examination prior to fiscal year
2018. Income tax examinations in Massachusetts (fiscal years 2016-2017) and California (fiscal years 2017-2018) were settled
in fiscal 2022. The amounts assessed were fully accrued.
In fiscal 2022, the Company received $422.6 million in refunds related to federal and state carryback claims, including
interest. At September 25, 2021, $404.9 million of these federal and state carryback claims was recorded as a current tax
receivable and included in prepaid expenses and other current assets in the Consolidated Balance Sheet.
The Company has determined that unremitted foreign earnings are not considered indefinitely reinvested to the extent
foreign earnings can be distributed without a significant tax cost. As such, the Company records foreign withholding tax
liabilities related to the future repatriation of such earnings. The Company continues to indefinitely reinvest all other outside
basis differences to the extent reversal would incur a significant tax liability. It is not practicable for the Company to calculate
the unrecognized deferred tax liability related to such incremental tax costs on those outside basis differences.
The Tax Cuts and Jobs Act of 2017
The Tax Cuts and Jobs Act of 2017 currently requires taxpayers to capitalize research and experimental expenditures
effective for tax years beginning after December 31, 2021 and amortize the capitalized costs over a period of 5 or 15 years
depending on where the research is conducted. If the capitalization requirement is not modified or repealed, the Company
expects the capitalization of research and experimental expenditures to increase its fiscal 2023 U.S. federal and state income tax
liabilities. The Company does not expect a significant impact to its effective tax rate related to this change.
Other Tax Accounting Pronouncements
ASU 2016-16 removes the prohibition in ASC 740 against the immediate recognition of the current and deferred income
tax effects of intra-entity transfers of assets other than inventory. In accordance with ASU 2016-16, the Company recorded a
$77.2 million increase to current income tax expense, a $39.4 million increase to current income tax liabilities, a $37.8 million
increase to long-term liabilities, and a $90.8 million decrease to deferred tax expense and net deferred tax liabilities related to
an internal restructuring for the year ended September 24, 2022. The net result was an increase to net income of $13.6 million,
or $0.05 to diluted net income per share.
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Non-Income Tax Matters
The Company is subject to tax examinations for value added, sales-based, payroll and other non-income tax items. A
number of these examinations are ongoing in various jurisdictions. The Company takes certain non-income tax positions in the
jurisdictions in which it operates and records loss contingencies pursuant to ASC 450, Contingencies. In the normal course of
business, the Company's positions and conclusions related to its non-income tax positions could be challenged, resulting in
assessments by governmental authorities. While the Company believes estimated losses previously recorded are reasonable,
certain audits are still ongoing and additional charges could be recorded in the future.
During the fourth quarter of fiscal 2021, based in part on developments in an ongoing tax audit as well as ongoing
operations, the Company determined that it was probable it had incurred a loss related to a non-income tax issue. The Company
estimated the probable amount of additional loss to be $11.2 million through fiscal 2021 and recorded this charge to general and
administrative expenses. While the Company believes its estimate is reasonable and appropriate, the matter is still ongoing and
additional charges could be recorded in the future.
10. Stockholders' Equity and Stock-Based Compensation
Stock Repurchase Program
On June 13, 2018, the Board of Directors authorized the repurchase of up to $500.0 million of the Company's outstanding
common stock. This share repurchase plan was effective August 1, 2018 and expired March 27, 2020. Under this authorization,
during fiscal 2019, the Company repurchased 4.8 million shares of its common stock for total consideration of $200.1 million.
During the first and second quarters of fiscal 2020, the Company repurchased 3.9 million shares of its common stock for a total
consideration of $210.9 million. As of March 28, 2020, the Company had completed this authorization.
On November 19, 2019, the Board of Directors authorized the Company to repurchase up to $205 million of its
outstanding shares pursuant to an accelerated share repurchase ("ASR") agreement. On November 22, 2019, the Company
executed the ASR agreement with Goldman Sachs & Co. ("Goldman Sachs") pursuant to which the Company repurchased
$205 million of the Company's common stock. The initial delivery of approximately 80% of the shares under the ASR was
3.3 million shares for which the Company initially allocated $164.0 million of the $205 million paid to Goldman Sachs during
the first quarter of fiscal 2020. The Company evaluated the nature of the forward contract aspect of the ASR under ASC 815
and concluded equity classification was appropriate. Final settlement of the transaction under the ASR occurred in the second
quarter of fiscal 2020. At settlement, Goldman Sachs delivered an additional 0.6 million shares of the Company's common
stock.
On December 11, 2019, the Board of Directors authorized a new share repurchase plan to repurchase up to $500.0 million
of the Company's outstanding common stock, effective at the beginning of the third quarter of fiscal 2020. On March 2, 2020
the Board of Directors approved accelerating the effective date of the new share repurchase plan from March 27, 2020 to March
2, 2020. Under this revised authorization during fiscal 2020, the Company repurchased 5.1 million shares of its common stock
for a total consideration of $237.7 million. During the first quarter of fiscal 2021, the Company repurchased 1.5 million shares
of its common stock under this plan for a total consideration of $101.3 million.
On December 9, 2020, the Board of Directors authorized a new five-year share repurchase program to repurchase up to
$1.0 billion of the Company's outstanding common stock. The prior program was terminated in connection with this new
authorization. Under the authorization, during fiscal 2021, the Company repurchased 4.6 million shares of its common stock for
a total consideration of $308.5 million. During fiscal 2022, the Company repurchased an additional 7.7 million shares of its
common stock for a total consideration of $542.1 million.
On September 22, 2022, the Board of Directors authorized a new stock repurchase program, with a five-year term, to
repurchase up to $1.0 billion of the Company’s outstanding common stock, effective as of the close of trading on September 23,
2022. This new stock repurchase program replaced the previous $1.0 billion authorization. Subsequent to September 24, 2022,
under the new stock repurchase program, the Company repurchased 1.5 million shares of its common stock for $100.0 million.
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Stock-Based Compensation
Equity Compensation Plans
The Company has one share-based compensation plan pursuant to which awards are currently being issued—the 2008
amended and restated Equity Incentive Plan (“2008 Equity Plan”). The purpose of the 2008 Equity Plan is to provide stock
options, restricted stock units and other equity interests in the Company to employees, officers, directors, consultants and
advisors of the Company and any other person who is determined by the Board of Directors to have made (or is expected to
make) contributions to the Company. The 2008 Equity Plan is administered by the Board of Directors of the Company, and a
total of 31.5 million shares were reserved for issuance under this plan. As of September 24, 2022, the Company had 3.3 million
shares available for future grant under the 2008 Equity Plan.
The following presents stock-based compensation expense in the Company’s Consolidated Statements of Operations in
fiscal 2022, 2021 and 2020:
Cost of revenues
Research and development
Selling and marketing
General and administrative
Restructuring
2022
2021
2020
$
$
9.1 $
8.8
10.5
38.3
—
66.7 $
8.0 $
7.7
9.5
38.9
0.9
65.0 $
6.7
8.0
10.2
50.9
7.5
83.3
Grant-Date Fair Value
The Company uses a binomial model to determine the fair value of its stock options. The Company considers a number of
factors to determine the fair value of options including the assistance of an outside valuation adviser. Information pertaining to
stock options granted during fiscal 2022, 2021 and 2020 and related assumptions are noted in the following table:
Options granted (in millions)
Weighted-average exercise price
Weighted-average grant date fair value
Assumptions:
Risk-free interest rates
Expected life (in years)
Expected volatility
Dividend yield
Years ended
September 24,
2022
September 25,
2021
September 26,
2020
0.7
71.07
21.01
$
$
0.6
68.62
19.86
$
$
1.0
45.96
13.92
$
$
1.1 %
4.8
34.2 %
—
0.4 %
4.8
35.0 %
—
1.7 %
4.8
33.6 %
—
The risk-free interest rate is based on a treasury instrument whose term is consistent with the expected life of the stock
options. In projecting expected stock price volatility, the Company uses a combination of historical stock price volatility and
implied volatility from observable market prices of similar equity instruments. The Company estimated the expected life of
stock options based on historical experience using employee exercise and option expiration data.
Stock-Based Compensation Expense Attribution
The Company uses the straight-line attribution method to recognize stock-based compensation expense for stock options
and restricted stock units ("RSUs"), unless the employee meets the plan retirement provision of reaching a certain age and years
of service criteria in which case the expense is accelerated to match the required service period to receive such benefit. The
vesting term of stock options is generally four years with annual vesting of 25% per year on the anniversary of the grant date,
and RSUs generally vest over three years with annual vesting at 33% per year on the anniversary of the grant date.
The amount of stock-based compensation recognized during a period is based on the value of the portion of the awards
that are ultimately expected to vest. Under ASC 718, the Company's accounting policy is to estimate forfeitures at the time
awards are granted and revise, if necessary, in subsequent periods if actual forfeitures differ from those estimates. Based on an
analysis of historical forfeitures, the Company has determined a specific forfeiture rate for certain employee groups and has
applied forfeiture rates ranging from 0% to 6.0% as of September 24, 2022 depending on the specific employee group. This
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analysis is re-evaluated annually and the forfeiture rate adjusted as necessary. Ultimately, the actual stock-based compensation
expense recognized will only be for those stock options and RSUs that vest.
Stock-based compensation expense related to stock options was $12.0 million, $13.0 million, and $15.5 million in fiscal
2022, 2021 and 2020, respectively. Stock compensation expense related to stock units, including RSUs, performance stock
units ("PSUs"), free cash flow performance stock units ("FCFs") and market stock units ("MSUs") was $48.2 million, $46.1
million, and $63.3 million in fiscal 2022, 2021 and 2020, respectively. The related tax benefit recorded in the Consolidated
Statements of Income was $8.6 million, $7.9 million and $9.5 million in fiscal 2022, 2021 and 2020, respectively. At
September 24, 2022, there was $15.2 million and $53.6 million of unrecognized compensation expense related to stock options
and stock units, respectively, to be recognized over a weighted average period of 2.2 years and 1.8 years, respectively.
Share Based Payment Activity
The following table summarizes all stock option activity under the Company’s stock option plans for the year ended
September 24, 2022:
Options outstanding at September 25, 2021
Granted
Canceled/ forfeited
Exercised
Options outstanding at September 24, 2022
Options exercisable at September 24, 2022
Options vested and expected to vest at September
24, 2022 (1)
Number
of Shares
(in millions)
Weighted-
Average
Exercise Price
4.2 $
0.7
(0.2)
(0.3)
4.4 $
2.8 $
44.66
71.07
59.36
41.32
48.46
41.57
4.3 $
48.38
Weighted-
Average
Remaining
Contractual Life
(in Years)
Aggregate
Intrinsic
Value
(in millions)
6.6 $
132.7
6.1 $
5.2 $
6.1 $
11.1
71.0
61.6
70.9
(1) This represents the number of vested stock options as of September 24, 2022 plus the unvested outstanding options at
September 24, 2022 expected to vest in the future, adjusted for estimated forfeitures.
During fiscal 2021 and 2020, the total intrinsic value of options exercised (i.e., the difference between the market price on
the date of exercise and the price paid by the employee to exercise the options) was $30.4 million and $44.8 million,
respectively.
A summary of the Company’s RSU, PSU, FCF and MSU activity during the year ended September 24, 2022 is presented
below:
Non-vested Shares
Non-vested at September 25, 2021
Granted
Vested
Forfeited
Non-vested at September 24, 2022
Number of
Shares
(in millions)
Weighted-Average
Grant-Date Fair
Value
1.7 $
1.0
(0.9)
(0.1)
1.7 $
54.21
71.45
50.03
55.24
64.43
The number of RSUs vested includes shares withheld on behalf of employees to satisfy minimum statutory tax
withholding requirements. The Company pays the minimum statutory tax withholding requirement on behalf of its employees.
During fiscal 2022, 2021 and 2020 the total fair value of RSUs vested was $43.8 million, $73.1 million and $34.9 million,
respectively.
The Company granted 0.7 million, 0.5 million and 0.6 million RSUs during fiscal 2022, 2021 and 2020, respectively. In
addition, included in the above chart, the Company also granted 0.1 million, 0.1 million and 0.1 million PSUs during fiscal
2022, 2021, and 2020, respectively, to members of the Company's senior management team, which includes additional shares
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issued upon achieving metrics within the performance criteria. The PSUs were valued at $71.16, $68.51 and $45.38 per share
based on the ending stock price on the date of grant in fiscal 2022, 2021 and 2020, respectively. Each recipient of the PSUs is
eligible to receive between zero and 200% of the target number of shares of the Company’s common stock at the end of three
year performance period provided the Company’s defined Return on Invested Capital metrics are achieved. The Company also
granted $0.1 million of FCF PSUs based on a three-year cumulative free cash flow measure (FCF) to its senior management
team in fiscal 2022. The Company granted 0.1 million and 0.1 million of FCF PSUs based on a one-year measurement period to
its senior management team in fiscal 2021 and 2020, respectively. Each recipient of FCF PSUs is eligible to receive between
zero and 200% of the target number of shares of the Company's common stock at the end of the three-year or one-year
measurement periods. The PSUs and FCF PSUs cliff-vest three years from the date of grant, and the Company recognizes
compensation expense ratably over the required service period based on its estimate of the number of shares that will vest upon
achieving the measurement criteria. If there is a change in the estimate of the number of shares that are probable of vesting, the
Company will cumulatively adjust compensation expense in the period that the change in estimate is made. The Company also
granted 0.1 million, 0.1 million and 0.1 million MSUs during fiscal 2022, 2021 and 2020, respectively, to its senior
management team. Each recipient of MSUs is eligible to receive between zero and 200% of the target number of shares of the
Company’s common stock at the end of three year performance period based upon achieving a certain total shareholder return
relative to a defined peer group. The MSUs were valued at $75.43, $82.31 and $43.54 per share using the Monte Carlo
simulation model in fiscal 2022, 2021 and 2020, respectively. These awards cliff-vest three years from the date of grant, and the
Company recognizes compensation expense for the MSUs ratably over the service period.
Employee Stock Purchase Plan
The Hologic, Inc. 2012 Employee Stock Purchase Plan (“2012 ESPP”) provides for the granting of up to 2.5 million
shares of the Company’s common stock to eligible employees. The 2012 ESPP plan period is semi-annual and allows
participants to purchase the Company’s common stock at 85% of the lower of (i) the market price per share of the common
stock on the first day of the offering period or (ii) the market price per share of the common stock on the purchase date. Stock-
based compensation expense in fiscal 2022, 2021 and 2020 was $6.5 million, $5.9 million and $4.5 million, respectively.
The Company uses the Black-Scholes model to estimate the fair value of shares to be issued as of the grant date using the
following weighted average assumptions:
Assumptions:
Risk-free interest rates
Expected life (in years)
Expected volatility
Dividend yield
September 24,
2022
September 25,
2021
September 26,
2020
0.96 %
0.5
34.0 %
—
0.26 %
0.5
34.1 %
—
1.32 %
0.5
26.9 %
—
11. 401(k) Plan
The Company's U.S. employees have access to a qualified 401(k) defined contribution plan. The Company made
contributions of $21.8 million, $20.9 million and $19.6 million for fiscal 2022, 2021 and 2020, respectively.
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12. Deferred Compensation Plans
Nonqualified Deferred Compensation Plan
Effective March 15, 2006, the Company adopted its Nonqualified Deferred Compensation Plan ("DCP") to provide non-
qualified retirement benefits to a select group of executive officers, senior management and highly compensated employees of
the Company. Eligible employees may elect to contribute up to 75% of their annual base salary and 100% of their annual bonus
to the DCP and such employee contributions are 100% vested. In addition, the Company may elect to make annual
discretionary contributions on behalf of participants in the DCP. Each Company contribution is subject to a three-year vesting
schedule, such that each contribution vests one third annually. Employee contributions are recorded within accrued expenses.
Upon enrollment into the DCP, employees make investment elections for both their voluntary contributions and
discretionary contributions, if any, made by the Company. Earnings and losses on contributions based on these investment
elections are recorded as a component of compensation expense in the period earned.
Annually, the Compensation Committee of the Board of Directors has approved a discretionary cash contribution to the
DCP for each year. Discretionary contributions by the Company to the DCP are held in a Rabbi Trust. The Company records
compensation expense for the DCP discretionary contributions ratably over the three-year vesting period of each annual
contribution, unless the participant meets the plan retirement provision of reaching a certain age and years of service criteria in
which case the expense is accelerated to match the required service period to receive such benefit. Under the DCP, the
Company recorded compensation expense related to Company contributions of $4.0 million, $3.2 million and $3.1 million in
fiscal 2022, 2021 and 2020, respectively. The full amount of the discretionary contribution, net of forfeitures, along with
employee deferrals is recorded within accrued expenses and totaled $61.8 million and $76.1 million at September 24, 2022 and
September 25, 2021, respectively.
The Company has purchased Company-owned group life insurance contracts, in which both voluntary and discretionary
Company DCP contributions are invested, to partially fund payment of the Company’s obligation to the DCP participants. The
total amount invested at September 24, 2022 and September 25, 2021 was $49.2 million and $64.3 million, respectively. The
values of these life insurance contracts are recorded in other long-term assets. Changes in the cash surrender value of life
insurance contracts, which were not significant in fiscal 2022, 2021 and 2020, are recorded within other income (expense), net.
Deferred Equity Plan
Effective September 17, 2015, the Company adopted the Hologic, Inc. Deferred Equity Plan (the “DEP”). The DEP is
designed to allow executives and non-employee Directors to accumulate Company stock in a tax-efficient manner to meet their
long-term equity accumulation goals and shareholder ownership guidelines. Under the DEP, eligible participants may elect to
defer the settlement of stock units granted under the 2008 Equity Plan until separation from service or separation from service
plus a fixed number of years. Participants may defer settlement by vesting tranche. Although the equity will vest on schedule, if
deferral of settlement is elected, no shares are issued until the settlement date. The settlement date is the earlier of death,
disability, change in control of the Company or separation from service plus the number of years of deferral elected by the
participant. While these shares upon vesting are not distributed to the individuals and are not outstanding, these shares are
included in basic weighted average shares outstanding used to calculate earnings per share.
13. Non-cancelable Purchase Commitments
The Company has certain non-cancelable purchase obligations primarily related to inventory purchases and diagnostics
instruments, primarily Panther systems, and to a lesser extent other operating expense commitments. These obligations are not
recorded in the Consolidated Balance Sheets. For reasons of quality assurance, sole source availability or cost effectiveness,
certain key components and raw materials and instruments are available only from a sole supplier and the Company has certain
long-term supply contracts to assure continuity of supply. At September 24, 2022, non-cancelable purchase commitments were
as follows:
Fiscal 2023
Fiscal 2024
Fiscal 2025
Fiscal 2026
Fiscal 2027
Thereafter
Total
302.9
45.4
12.5
2.8
2.7
0.3
366.6
$
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14. Litigation and Related Matters
On November 6, 2015, the Company filed a suit against Minerva Surgical, Inc. (“Minerva”) in the United States District
Court for the District of Delaware, alleging that Minerva’s endometrial ablation device infringes U.S. Patent 6,872,183 (the '183
patent), U.S. Patent 8,998,898 and U.S. Patent 9,095,348 (the '348 patent). On January 25, 2016, the Company amended the
complaint to include claims against Minerva for unfair competition, deceptive trade practices and tortious interference with
business relationships. On February 5, 2016, the Company filed a second amended complaint to additionally allege that
Minerva’s endometrial ablation device infringes U.S. Patent 9,247,989 (the '989 patent). On March 4, 2016, Minerva filed an
answer and counterclaims against the Company, seeking declaratory judgment on the Company’s claims and asserting claims
against the Company for unfair competition, deceptive trade practices, interference with contractual relationships, breach of
contract and trade libel. On June 2, 2016, the Court denied the Company’s motion for a preliminary injunction on its patent
claims and denied Minerva’s request for preliminary injunction related to the Company’s alleged false and deceptive statements
regarding the Minerva product. On June 28, 2018, the Court granted the Company's summary judgment motions on
infringement and no invalidity with respect to the ‘183 and ‘348 patents. The Court also granted the Company’s motion for
summary judgment on assignor estoppel, which bars Minerva’s invalidity defenses or any reliance on collateral findings
regarding invalidity from inter partes review proceedings. The Court also denied all of Minerva’s defenses, including its
motions for summary judgment on invalidity, non-infringement, no willfulness, and no unfair competition. On July 27, 2018,
after a two-week trial, a jury returned a verdict that: (1) awarded the Company $4.8 million in damages for Minerva’s
infringement; (2) found that Minerva’s infringement was not willful; and (3) found for the Company regarding Minerva’s
counterclaims. Damages continued to accrue as Minerva continued its infringing conduct. On May 2, 2019, the Court issued
rulings that denied the parties' post-trial motions, including the Company's motion for a permanent injunction seeking to
prohibit Minerva from selling infringing devices. Both parties appealed the Court's rulings regarding the post-trial motions. On
March 4, 2016, Minerva filed two petitions at the United States Patent and Trademark Office ("USPTO") for inter partes
review of the '348 patent. On September 12, 2016, the Patent Trial and Appeal Board of the USPTO ("PTAB") declined both
petitions to review patentability of the ‘348 patent. On April 11, 2016, Minerva filed a petition for inter partes review of the
'183 patent. On October 6, 2016, the PTAB granted the petition and instituted a review of the '183 patent. On December 15,
2017, the PTAB issued a final written decision invalidating all claims of the ‘183 patent. On February 9, 2018 the Company
appealed this decision to the United States Court of Appeals for the Federal Circuit ("Court of Appeals"). On April 19, 2019,
the Court of Appeals affirmed the PTAB's final written decision regarding the '183 patent. On July 16, 2019, the Court of
Appeals denied the Company’s petition for rehearing in the appeal regarding the '183 patent. On April 22, 2020, the Court of
Appeals affirmed the district court’s summary judgment ruling in favor of the Company of no invalidity and infringement, and
summary judgment that assignor estoppel bars Minerva from challenging the validity of the ‘348 patent. The Court of Appeals
also denied the Company’s motion for a permanent injunction and ongoing royalties for infringement of the ‘183 patent. The
Court of Appeals denied Minerva’s arguments for no damages or, alternatively, a new trial. On May 22, 2020 both parties
petitioned for en banc review of the Court of Appeals decision. On July 22, 2020, the Court of Appeals denied both parties'
petitions for en banc review. On August 28, 2020, the district court entered final judgment against Minerva but stayed execution
pending resolution of Minerva’s intent to petition for Supreme Court review. On September 30, 2020, Minerva filed a petition
requesting Supreme Court review on the issue of assignor estoppel. On November 5, 2020, the Company filed a cross- petition
requesting Supreme Court review on the issue of assignor estoppel. On January 8, 2021, the Supreme Court granted Minerva's
petition to address the issue of assignor estoppel and denied the Company's petition. Oral argument before the Supreme Court
was held on April 21, 2021. On June 29, 2021, the Supreme Court ruled 5-4 to uphold the assignor estoppel but limited its
application to situations in which an assignor's claim of invalidity contradicts a prior representation the assignor made in
assigning the patent. The Court also vacated the ruling of the Court of Appeals and remanded the case for further proceedings
consistent with its opinion. On August 11, 2022, the Court of Appeals affirmed the district court ruling on the issue of assignor
estoppel, which barred Minerva from challenging the validity of the patent rights it assigned to the Company, and reinstated its
earlier judgment against Minerva on infringement. On September 11, 2022, Minerva petitioned for en banc review of the Court
of Appeals decision. The Company filed its response on October 25, 2022, and on November 10, 2022, the Court of Appeals
denied Minerva's petition.
On April 11, 2017, Minerva filed suit against the Company and Cytyc Surgical Products, LLC (“Cytyc”) in the United
States District Court for the Northern District of California alleging that the Company’s and Cytyc’s NovaSure ADVANCED
endometrial ablation device infringes Minerva’s U.S. patent 9,186,208 (the '208 patent). Minerva is seeking a preliminary and
permanent injunction against the Company and Cytyc from selling this NovaSure device as well as enhanced damages and
interest, including lost profits, price erosion and/or royalty. On January 5, 2018, the Court denied Minerva's motion for a
preliminary injunction. On February 2, 2018, at the parties’ joint request, this action was transferred to the District of Delaware.
On March 26, 2019, the Magistrate Judge issued a claims construction ruling regarding the disputed terms in the patent, which
the District Court Judge adopted in all respects on October 21, 2019. The original trial date of July 20, 2020 was vacated. On
October 21, 2020, the trial court scheduled a 10 day trial beginning on August 9, 2021. On July 27. 2021, the Delaware district
court granted Hologic's motion for summary judgment on invalidity of the '208 patent and entered judgment in favor of the
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Company. On August 24, 2021, Minerva appealed this and the other rulings to the Court of Appeals. An oral argument was
held on October 3, 2022. At this time, based on available information regarding this litigation, the Company is unable to
reasonably assess the ultimate outcome of this case or determine an estimate, or a range of estimates, of potential losses.
The Company is a party to various other legal proceedings and claims arising out of the ordinary course of its business.
The Company believes that except for those matters described above there are no other proceedings or claims pending against it
the ultimate resolution of which could have a material adverse effect on its financial condition or results of operations. In all
cases, at each reporting period, the Company evaluates whether or not a potential loss amount or a potential range of loss is
probable and reasonably estimable under ASC 450. Legal costs are expensed as incurred.
15. Disposition
Sale of Medical Aesthetics
On November 20, 2019, the Company entered into a definitive agreement to sell its Medical Aesthetics business to
Clayton Dubilier & Rice ("CD&R") for a sales price of $205.0 million in cash, less certain adjustments. The sale was completed
on December 30, 2019, and the Company received cash proceeds of $153.4 million in the second quarter of fiscal 2020. The
sale price was subject to adjustment pursuant to the terms of the definitive agreement, and in the fourth quarter of fiscal 2020
the parties agreed to a final sales price of $150.0 million. The Company agreed to provide certain transition services for three to
fifteen months, depending on the nature of the service. The Company also agreed to indemnify CD&R for certain legal and tax
matters that existed as of the date of disposition. In connection with its accounting for the sale, the Company recorded
indemnification liabilities of $10.9 million within accrued expenses associated with its obligations under the sale agreement.
As a result of this transaction, the Medical Aesthetics asset group was designated as assets held-for-sale in the first
quarter of fiscal 2020. Pursuant to ASC 360, Impairment and Disposal of Long-Lived Assets, asset groups under this
designation are required to be recorded at fair value less costs to sell. The Company determined that this disposal did not
qualify as a discontinued operation as the sale of the Medical Aesthetics business was deemed to not be a strategic shift having
or that will have a major effect on the Company's operations and financial results. Based on the terms in the agreement of the
sales price and formula for net working capital and related adjustments, its estimate of the fair value for transition services and
the amount that must be carved out of the sale proceeds, and liabilities the Company will retain or for which it has agreed to
indemnify CD&R, the Company recorded an impairment charge of $30.2 million in the first quarter of fiscal 2020. The
impairment charge was allocated to Medical Aesthetics long-lived assets, of which $25.8 million was allocated to cost of
product revenues and $4.4 million to operating expenses.
Loss from operations of the disposed business presented below represents the operating loss of the business as it was
operated prior to the date of disposition. The operating expenses include only those that were incurred directly by and were
retained by the disposed business. As noted above, the Company had performed a number of transition services and the
financial impact from these services is not included in the amount presented below. In addition, the Company continued to
incur expenses related to this business under the indemnification provisions primarily related to legal and tax matters that
existed as of the date of disposition. Subsequent to the disposition, the Company recorded additional expenses of $6.2 million in
fiscal 2020 primarily for accelerated stock compensation, inventory reserves under the manufacturing supply agreement, and
legal expenses and settlements, which are not included in the below amounts. Loss from operations of the disposed business for
fiscal 2020 was as follows:
Loss from operations
Year Ended
September 26, 2020
$
(46.5)
16. Business Segments and Geographic Information
The Company reports segment information in accordance with ASC 280, Segment Reporting. Operating segments are
identified as components of an enterprise about which separate, discrete financial information is available for evaluation by the
chief operating decision maker, or decision-making group, in making decisions about how to allocate resources and assess
performance. The Company’s chief operating decision maker is its chief executive officer, and the Company’s reportable
segments have been identified based on the types of products manufactured and the end markets to which the products are sold.
Each reportable segment generates revenue from either the sale of medical equipment and related services and/or sale of
disposable supplies, primarily used for diagnostic testing and surgical procedures. During fiscal 2022 and fiscal 2021, the
Company had four reportable segments: Diagnostics, Breast Health, GYN Surgical and Skeletal Health. During the first quarter
of fiscal 2020, the Company had five reportable segments: Diagnostics, Breast Health, Medical Aesthetics, GYN Surgical and
Skeletal Health. The Company completed the sale of its Medical Aesthetics business on December 30, 2019. The Company
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measures and evaluates its reportable segments based on segment revenues and operating income adjusted to exclude the effect
of non-cash charges, such as intangible asset amortization expense, goodwill and intangible asset impairment charges,
transaction and integration expenses for acquisitions, restructuring, consolidation and divestiture charges, litigation charges, and
other one-time or unusual items.
Identifiable assets for the reportable segments consist of inventories, intangible assets, goodwill, and property, plant and
equipment. The Company fully allocates depreciation expense to its reportable segments. The Company has presented all other
identifiable assets as corporate assets. There were no intersegment revenues. Segment information for fiscal 2022, 2021, and
2020 was as follows:
Total revenues:
Diagnostics
Breast Health
GYN Surgical
Skeletal Health
Medical Aesthetics
Operating income (loss):
Diagnostics
Breast Health
GYN Surgical
Skeletal Health
Medical Aesthetics
Depreciation and amortization:
Diagnostics
Breast Health
GYN Surgical
Skeletal Health
Medical Aesthetics
Capital expenditures:
Diagnostics
Breast Health
GYN Surgical
Skeletal Health
Medical Aesthetics
Corporate
Identifiable assets:
Diagnostics
Breast Health
GYN Surgical
Skeletal Health
Corporate
September 24,
2022
Years ended
September 25,
2021
September 26,
2020
$
3,018.5 $
3,695.0 $
1,227.8
522.9
93.6
—
1,352.3
488.1
96.9
—
2,102.1
1,151.9
376.1
81.0
65.3
$
$
$
$
$
$
$
$
4,862.8 $
5,632.3 $
3,776.4
1,359.4 $
2,140.1 $
183.2
104.9
(7.3)
—
284.2
58.9
(2.9)
—
929.7
192.8
42.0
(2.4)
(57.1)
1,640.2 $
2,480.3 $
1,105.0
274.0 $
260.4 $
237.3
58.8
96.6
0.7
—
52.7
93.1
0.7
—
48.8
85.1
0.7
4.1
430.1 $
406.9 $
376.0
96.8 $
14.6
12.8
0.3
—
2.7
147.7 $
14.2
14.5
0.3
—
1.0
110.7
22.4
17.9
0.2
1.4
3.8
127.2 $
177.7 $
156.4
2,881.7 $
3,348.8 $
1,245.8
1,461.5
27.5
3,454.7
1,233.9
1,369.7
31.9
2,935.6
2,161.4
1,200.9
1,438.7
38.9
2,355.9
7,195.8
$
9,071.2 $
8,919.9 $
F-55
Table of Contents
The Company operates in the following major geographic areas as noted in the below chart. Revenue data is based
upon customer location. Other than the United States, no single country accounted for more than 10% of consolidated revenues.
The Company’s sales in Europe are predominantly derived from France, Italy, the Netherlands, the United Kingdom and
Germany. The Company’s sales in Asia-Pacific are predominantly derived from China, Australia and Japan. The “Rest of
world” designation includes Canada, Latin America and the Middle East.
Revenues by geography as a percentage of total revenues were as follows:
United States
Europe
Asia-Pacific
Rest of world
September 24,
2022
Years ended
September 25,
2021
September 26,
2020
71.3 %
18.3 %
7.4 %
3.0 %
100.0 %
69.3 %
21.3 %
6.5 %
2.9 %
100.0 %
75.8 %
15.1 %
6.0 %
3.1 %
100.0 %
The Company’s property, plant and equipment, net were geographically located as follows:
United States
Europe
Costa Rica
Rest of world
September 24,
2022
September 25,
2021
September 26,
2020
$
$
332.4 $
103.8
32.1
13.3
481.6 $
403.2 $
122.9
26.9
11.7
564.7 $
383.0
77.5
20.8
10.2
491.5
17. Accrued Expenses and Other Long-Term Liabilities
Accrued expenses and other long-term liabilities consisted of the following:
Accrued Expenses
Compensation and employee benefits
Income and other taxes
Operating leases
Contingent consideration
Accrued interest
Other
Other Long-Term Liabilities
Reserve for income tax uncertainties
Operating leases
Contingent consideration
Interest rate swap
Pension liabilities
Other
F-56
September 24,
2022
September 25,
2021
$
$
292.2 $
44.2
23.2
12.0
7.3
156.4
535.3 $
297.2
70.9
26.8
16.3
16.9
168.1
596.2
September 24,
2022
September 25,
2021
$
$
251.6 $
53.8 $
11.4 $
—
6.8
7.1
330.7 $
210.0
66.1
58.8
7.6
10.0
16.2
368.7
Table of Contents
F-57
Subsidiaries of Hologic*
Jurisdiction of Incorporation or Organization
Exhibit 21.1
Acessa Health Inc.
Beijing Hologic Technology Co., Ltd.
Benassar Diagnostica-Equipamientos Medicos Unipessoal, Lda.
BioLucent, LLC
Bioptics, Inc.
Biotheranostics, Inc.
Bolder Surgical Holdings, Inc.
Bolder Surgical, LLC
Cytyc Corporation
Cytyc Prenatal Products Corp.
Cytyc Surgical Products, LLC
Diagenode Co., Ltd.
Diagenode SA
Diagenode SPA
Diagenode, LLC
Direct Radiography Corp.
Emsor, Sociedad de responsabilidad limitada
Faxitron Bioptics, LLC
Genewave SAS
Gen-Probe Incorporated
Gen-Probe Prodesse, Inc.
Health Beacons, Inc.
Hologic (Australia & New Zealand) Pty Ltd.
Hologic (Hainan) Medical Co., Ltd.
Hologic ASE, LLC
Hologic Asia Limited
Hologic Asia Pacific Limited
Hologic Austria GmbH
Hologic BV
Hologic Bermuda Limited
Hologic Canada ULC
Hologic Denmark ApS
Hologic Deutschland GmbH
Hologic Espana S.A.
Hologic Finance Ltd.
Hologic France SARL
Hologic GGO 2, LLC
Hologic GGO 3 LLP
Hologic GGO 4 LTD
Hologic Global Holding LTD
Hologic Hitec-Imaging GmbH
Hologic Holdings Limited
Hologic HUB LTD
Hologic Iberia, S.L.
Delaware
China
Portugal
Delaware
Arizona
Delaware
Delaware
Colorado
Delaware
Delaware
Massachusetts
Japan
Belgium
Chile
Delaware
Delaware
Spain
Delaware
France
Delaware
Wisconsin
Washington
Australia
China
Delaware
Hong Kong
Hong Kong
Austria
Belgium
Bermuda
Canada
Denmark
Germany
Spain
Bermuda
France
Delaware
United Kingdom
United Kingdom
United Kingdom
Germany
United Kingdom
United Kingdom
Spain
Subsidiaries of Hologic*
Jurisdiction of Incorporation or Organization
Hologic India LLP
Hologic International Holdings B.V.
Hologic IP LTD
Hologic Ireland Limited
Hologic Italia S.r.l.
Hologic Japan KK
Hologic Korea Ltd.
Hologic Latin America (Servicos Em Marketing E Negocios) Ltda.
Hologic Ltd.
Hologic Malaysia SDN. BHD.
Hologic Medical Technologies (Beijing) Co., Ltd.
Hologic Medicor GmbH
Hologic Medicor Suisse GmbH
Hologic Netherlands B.V.
Hologic Nordic Holdings Oy
Hologic (Shanghai) Medical Supplies Co., Ltd.
Hologic Sales and Service, LLC
Hologic Singapore Pte. Ltd
Hologic Suisse SA
Hologic Surgical Products Costa Rica, S.R.L.
Hologic Sweden AB
Hologic Taiwan Ltd.
Hologic UK Finance Ltd.
Hologic US Finance Co LLC
Mobidiag Oy
Mobidiag Sverige AB
Mobidiag UK Ltd.
Navigation Three Limited
Somatex (HK) Limited
Somatex Medical Technologies GmbH
SuperSonic Imagine SA
SuperSonic Imagine GmbH
SuperSonic Imagine Ltd
India
Netherlands
United Kingdom
Ireland
Italy
Japan
Korea
Brazil
United Kingdom
Malaysia
China
Germany
Switzerland
Netherlands
Finland
China
Massachusetts
Singapore
Switzerland
Costa Rica
Sweden
Taiwan
United Kingdom
Delaware
Finland
Sweden
United Kingdom
Hong Kong
China
Germany
France
Germany
United Kingdom
SuperSonic Imagine (Shanghai) Medical Devices Co., Ltd.
China
Suros Surgical Systems, Inc.
TCT International Co., Ltd.
Delaware
British Virgin Islands
*Subsidiaries not included in the list are omitted because, in aggregate, they are insignificant as defined by Item 601(b)(21) of
Regulation S-K.
We consent to the incorporation by reference in the following Registration Statements:
Consent of Independent Registered Public Accounting Firm
Exhibit 23.1
(1) Registration Statement (Form S-3ASR No. 333-235287) pertaining to Hologic, Inc.’s shelf registration
statement for common stock, preferred stock, debt securities, rights, warrants, purchase contracts, units or
any combination of the foregoing, and
(2) Registration Statements (Form S-8 Nos. 333-150796, 333-181126, 333-188468, 333-210968,
333-224613) pertaining to the equity incentive plans and employee stock purchase plan of Hologic, Inc.;
of our reports dated November 15, 2022, with respect to the consolidated financial statements of Hologic, Inc. and the
effectiveness of internal control over financial reporting of Hologic, Inc., included in this Annual Report (Form 10-K) of
Hologic, Inc. for the year ended September 24, 2022.
/s/ Ernst & Young LLP
Boston, Massachusetts
November 15, 2022
CERTIFICATION PURSUANT TO SECTION 302 OF THE SARBANES-OXLEY ACT OF 2002
Exhibit 31.1
I, Stephen P. MacMillan, certify that:
1.
I have reviewed this annual report on Form 10-K of Hologic, 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)) and internal control over financial reporting (as
defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) 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: November 15, 2022
/s/ Stephen P. MacMillan
Stephen P. MacMillan
Chairman, President and Chief Executive Officer
CERTIFICATION PURSUANT TO SECTION 302 OF THE SARBANES-OXLEY ACT OF 2002
Exhibit 31.2
I, Karleen M. Oberton, certify that:
1.
I have reviewed this annual report on Form 10-K of Hologic, 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)) and internal control over financial reporting (as
defined in Exchange Act Rules 13a-15(f) and 15d-15(f)) 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: November 15, 2022
/s/ Karleen M. Oberton
Karleen M. Oberton
Chief Financial Officer
Certification
Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
(Subsections (a) and (b) of Section 1350, Chapter 63 of Title 18, United States Code)
Exhibit 32.1
I, Stephen P. MacMillan, Chief Executive Officer of Hologic, Inc., a Delaware corporation (the “Company”), do hereby
certify, pursuant to Section 906 of the Sarbanes-Oxley Act of 2002 (subsections (a) and (b) of Section 1350, Chapter 63 of Title
18, United States Code), that:
(1) The Annual Report on Form 10-K for the year ended September 24, 2022 (the “Form 10-K”) of the Company fully
complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and
(2) The information contained in the Form 10-K fairly presents, in all material respects, the financial condition and
results of operations of the Company.
Dated: November 15, 2022
/s/ Stephen P. MacMillan
Stephen P. MacMillan
Chairman, President and Chief Executive Officer
A SIGNED ORIGINAL OF THIS WRITTEN STATEMENT REQUIRED BY SECTION 906 OF THE SARBANES-OXLEY
ACT OF 2002 HAS BEEN PROVIDED TO HOLOGIC, INC. AND WILL BE RETAINED BY HOLOGIC, INC. AND
FURNISHED TO THE SECURITIES AND EXCHANGE COMMISSION OR ITS STAFF UPON REQUEST.
Certification
Pursuant to Section 906 of the Sarbanes-Oxley Act of 2002
(Subsections (a) and (b) of Section 1350, Chapter 63 of Title 18, United States Code)
Exhibit 32.2
I, Karleen M. Oberton, Chief Financial Officer of Hologic, Inc., a Delaware corporation (the “Company”), do hereby
certify, pursuant to Section 906 of the Sarbanes-Oxley Act of 2002 (subsections (a) and (b) of Section 1350, Chapter 63 of Title
18, United States Code), that:
(1) The Annual Report on Form 10-K for the year ended September 24, 2022 (the “Form 10-K”) of the Company fully
complies with the requirements of Section 13(a) or 15(d) of the Securities Exchange Act of 1934; and
(2) The information contained in the Form 10-K fairly presents, in all material respects, the financial condition and
results of operations of the Company.
Dated: November 15, 2022
/s/ Karleen M. Oberton
Karleen M. Oberton
Chief Financial Officer
A SIGNED ORIGINAL OF THIS WRITTEN STATEMENT REQUIRED BY SECTION 906 OF THE SARBANES-OXLEY
ACT OF 2002 HAS BEEN PROVIDED TO HOLOGIC, INC. AND WILL BE RETAINED BY HOLOGIC, INC. AND
FURNISHED TO THE SECURITIES AND EXCHANGE COMMISSION OR ITS STAFF UPON REQUEST.