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Beyond AirUNITED STATESSECURITIES AND EXCHANGE COMMISSIONWashington, DC 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 June 30, 2017 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: 1-10986 MISONIX, INC.(Exact name of registrant as specified in its charter) New York 11-2148932(State or other jurisdiction of incorporation ororganization) (I.R.S. Employer Identification No.) 1938 New Highway, Farmingdale, New York 11735(Address of principal executive offices) (Zip Code) Registrant’s telephone number, including area code: (631) 694-9555 Securities registered pursuant to Section 12(b) of the Act: Title of each class Name of each exchange on which registeredCommon Stock, $.01 par value Nasdaq Global 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 1934during 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 filingrequirements for the past 90 days.☑ Yes ☐ No Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive Data File required tobe submitted and posted pursuant to Rule 405 of Regulation S-T (§ 232.405 of this chapter) during the preceding 12 months (or for such shorter period thatthe registrant was required to submit and post such files). ☑ Yes ☐ No Indicate by check mark if disclosure of delinquent filers pursuant to Item 405 of Regulation S-K (§229.405 of this chapter) is not contained herein, and willnot be contained, to the best of registrant’s knowledge, in definitive proxy or information statements incorporated by reference in Part III of this Form 10-K orany amendment to this Form 10-K. ☐ Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, smaller reporting company or anemerging 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): Large acceleratedfiler ☐ Accelerated filer ☑Non-accelerated filer ☐ Smaller reporting company ☐ Emerging growthcompany ☐ (Do not check if a smaller reportingcompany) 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 orrevised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐ Indicate by check mark whether the registrant is a shell company (as defined in Rule 12b-2 of the Exchange Act).☐ Yes ☑ No The aggregate market value of the voting stock held by non-affiliates of the registrant on December 31, 2016 (computed by reference to the closing price ofsuch stock on such date) was approximately $89,360,935. There were 9,357,166 shares of Common Stock outstanding at August 24, 2017. DOCUMENTS INCORPORATED BY REFERENCE None USE OF FORWARD-LOOKING STATEMENTS In this document, we refer to Misonix, Inc. and its subsidiaries (unless the context otherwise requires) as “we,” the “Company” or “Misonix.” With theexception of historical information contained in this Form 10-K, content herein may contain “forward looking statements” that are made pursuant to the SafeHarbor Provisions of the Private Securities Litigation Reform Act of 1995. These statements are based on management’s current expectations and are subjectto uncertainty and changes in circumstances. We cannot guarantee that any forward looking statements will be accurate, although we believe that we havebeen reasonable in our expectations and assumptions. Investors should realize that if underlying assumptions prove inaccurate or unknown risks oruncertainties materialize, actual results could vary materially from our expectations and projections. These factors include general economic conditions,delays and risks associated with the performance of contracts, risks associated with international sales and currency fluctuations, uncertainties as a result ofresearch and development, acceptable results from clinical studies, including publication of results and patient/procedure data with varying levels ofstatistical relevance, risks involved in introducing and marketing new products, regulatory compliance, potential acquisitions, consumer and industryacceptance, litigation and/or contemplated 510(k) filings, the ability to achieve and maintain profitability in our business lines, and other factors discussedin this Annual Report on Form 10-K, subsequent Quarterly Reports on Form 10-Q and Current Reports on Form 8-K. We disclaim any obligation to updateany forward-looking statements. 2 TABLE OF CONTENTS PART I4Item 1.Business4Item 1A.Risk Factors7Item 1B.Unresolved Staff Comments14Item 2.Properties14Item 3.Legal Proceedings15Item 4.Mine Safety Disclosures17PART II16Item 5.Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity Securities16Item 6.Selected Financial Data17Item 7.Management’s Discussion and Analysis of Financial Condition and Results of Operations17Item 7A.Quantitative and Qualitative Disclosures About Market Risk25Item 8.Financial Statements and Supplemental Data25Item 9.Changes in and Disagreements With Accountants on Accounting and Financial Disclosure25Item 9A.Controls and Procedures25Item 9B.Other Information27PART III28Item 10.Directors, Executive Officers and Corporate Governance28Item 11.Executive Compensation32Item 12.Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters44Item 13.Certain Relationships and Related Transactions, and Director Independence46Item 14.Principal Accountant Fees and Services47PART IV48Item 15.Exhibits and Financial Statement Schedules48Item 16.Form 10-K Summary51SIGNATURES52 3 PART I Item 1. Business Overview Misonix, Inc. is a New York corporation which, through its predecessors, was first organized in 1959. We design, manufacture, develop and market minimallyinvasive therapeutic ultrasonic medical devices. Our products enhance clinical outcomes and provide value to the overall healthcare system. Since wecommercialized our ultrasonic vessel sealing system with US Surgical in 1996, we have helped create a multi-billion dollar segment within the overallgeneral surgical and gynecological arena. We believe that our current focus products have the ability to become standard of care and provide the Companywith a steady recurring revenue stream. ●BoneScalpel ® surgical system (“BoneScalpel”), which is used mainly for surgical procedures involving the precise cutting and sculptingof bone while sparing soft tissue. BoneScapel is now recognized by surgeons globally as one of the most important surgical devicesenabling improved patient outcomes in the spinal arena. ●SonaStar ® Surgical Aspirator (“SonaStar”), which is used to emulsify and remove soft and hard tumors, primarily in the neuro and generalsurgery field. ●SonicOne® Wound Cleansing and Debridement System (“SonicOne”), which offers tissue specific debridement and cleansing of woundsand burns for effective removal of devitalized tissue and fibrin deposits while sparing viable cells. These devices primarily serve the following clinical specialties: neurosurgery, orthopedic surgery, plastic surgery, wounds and maxillo-facial. In the United States, our products are marketed primarily through a hybrid sales approach. This includes direct sales representatives, managed by regionalsales managers and supported by company application specialists, along with independent distributors. Outside the United States, we sell BoneScalpel and SonaStar to specialty distributors who purchase products from us to resell to their clinical customer bases.We sell to all major markets in the Americas, Europe, Middle East, Asia Pacific and Africa and we plan to sell SonicOne into select international markets. Products All Misonix disposables function with proprietary consoles which essentially convert electrical current into ultrasonic energy via piezo electric crystals inorder for the relevant device to produce a therapeutic effect. BoneScalpel The BoneScalpel is a state of the art, ultrasonic bone cutting and sculpting system capable of making precise cuts with minimal necrosis, minimal burnartifact, minimal inflammation and minimal bone loss. The device is also capable of preserving surrounding soft tissue structures because of its unique abilityto differentiate soft tissue from rigid bone. This device can make precise linear or curved cuts, on any plane, with precision not normally associated withpowered instrumentation. The BoneScalpel offers the speed and convenience of a powered instrument without the dangers associated with conventionalrotary devices. The effect on surrounding soft tissue is minimal due to the elastic and flexible structure of healthy tissue. This is a significant advantage inanatomical regions like the spine where patient safety is of primary concern. In addition, the linear motion of the blunt, tissue-impacting tips avoidsaccidental ‘trapping’ of soft tissue while largely eliminating the high speed spinning and tearing associated with rotary power instruments. The BoneScalpelallows surgeons to improve on existing surgical techniques by creating new approaches to bone cutting and sculpting, leading to substantial time savingsand increased operation efficiencies. 4 The expanded BoneScalpel product platform will allow entry into dynamic market segments like MIS spine surgery. In the future, additional market nicheopportunities may exist in small bone surgery of the hand, foot or ankle. SonaStar The SonaStar system provides powerful precise aspiration following the ultrasonic ablation of hard or soft tissue. The SonaStar has been used for a widevariety of surgical procedures applying both open and minimally invasive approaches, including neurosurgery and liver surgery. The SonaStar may also beused with OsteoSculpt ® probe tips, which enable the precise shaping or shaving of bony structures that prevent open access to partially or completelyhidden soft tissue masses. SonicOne The SonicOne Ultrasonic Cleansing and Debridement System is a highly innovative, tissue specific approach for the effective removal of devitalized ornecrotic tissue and fibrin deposits while sparing viable, surrounding cellular structures. The tissue specific capability is, in part, due to the fact that healthyand viable tissue structures have a higher elasticity and flexibility than necrotic tissue and are more resistant to destruction from the impact effects ofultrasound. The ultrasonic debridement process separates devitalized tissue from viable tissue layers, allowing for a more defined treatment and, usually, areduced pain sensation. We believe SonicOne establishes a new standard in wound and burn bed preparation, the essential first step in the healing process,while contributing to a faster patient healing. Other Business and Medical Devices In October 1996, we entered into a license agreement with Medtronic Minimally Invasive Therapies (“MMIT”). The MMIT license covers the furtherdevelopment of our medical technology relating to vessel sealing products, which uses high frequency sound waves to coagulate and divide tissue for bothopen and laparoscopic surgery. We developed the AutoSonix product with MMIT under the agreement. As a result of this joint development, we co-owncertain patents with MMIT and MMIT paid us a 5% royalty on end user sales. The MMIT license gives MMIT exclusive worldwide marketing and salesrights for this technology and device. Total royalties from sales of this device worldwide were approximately $3,764,000, $3,903,000 and $4,162,000 for thefiscal years ended June 30, 2017, 2016 and 2015, respectively. The royalty is recorded as “other income” in our financial statements. Our license agreementwith MMIT expired in August 2017 and no further payments are due thereafter. High Intensity Focused Ultrasound Technology We sold our rights to the high intensity focused ultrasound technology to SonaCare Medical, LLC (“SonaCare”) in May 2010. We may receive up toapproximately $5.8 million in payment for the sale. SonaCare will pay us 7% of the gross revenues received from its sales of the (i) prostate product in Europeand (ii) kidney and liver products worldwide, until we have received payments of $3 million, and thereafter 5% of the gross revenues, up to an aggregatepayment of $5.8 million, all subject to a minimum annual royalty of $250,000. Cumulative payments through June 30, 2017 were $1,504,788. Other The Company’s distribution agreement with Mentor Corporation, a subsidiary of Johnson & Johnson, for the sale, marketing and distribution of the Lysonixsoft tissue aspirator used for cosmetic surgery has terminated. Sales continue on a limited non-contractual purchase order basis. Total sales of this device,which includes parts and service, were approximately $48,000, $45,000 and $264,000 for the fiscal years ended June 30, 2017, 2016 and 2015, respectively. 5 Customers For the fiscal years ended June 30, 2017, 2016 and 2015, Cicel (Beijing) Science and Tech Co. Ltd. (“Cicel”), the Company’s former Chinese distributor,accounted for 0.2%, 6.4%, and 13.4% of the Company’s net sales, respectively. We did not have any other customer that accounted for 10% or more of ournet sales during such periods. Research & Development As of June 30, 2017, our Research and Development (“R&D”) organization consisted of a staff of ten employees including engineers, technical and supportpersonnel. The in-house technical expertise includes mechanical engineering, acoustics, electrical engineering, software development and product design.The R&D group focuses principally on developing new products and supporting existing products. During the three years ended June 30, 2017, the Company incurred R&D expenses of $1,837,497, $1,839,479, and $1,592,923 and or 6.7%, 8.0% and 7.2%of sales, respectively. Revenue by Region The Company’s revenues are generated from various regions throughout the world. Sales by the Company outside the United States are made throughdistributors. Sales made in the United States are made primarily through representative agents. The following is an analysis of net sales from continuingoperations by geographic region: For the years ended June 30, Net Change 2017 2016 2015 2017 2016 Domestic $16,460,771 $13,086,806 $10,797,920 25.8% 21.2%International 10,809,192 10,026,388 11,406,658 7.8% (12.1)%Total $27,269,963 $23,113,194 $22,204,578 18.0% 4.1% Our international sales include a concentration in China, aggregating $1,335,667, $1,557,132, and $2,974,086 for the fiscal years ended June 30, 2017, 2016and 2015, respectively. Manufacturing and Supply The Company manufactures and assembles its medical device products at its production facility located in Farmingdale, New York. The Company’s productsinclude components manufactured by other companies in the United States. The Company is not dependent upon any single source of supply and has nolong-term supply agreements. The Company believes that it will not encounter difficulty in obtaining materials, supplies and components adequate for itsanticipated short-term needs. Competition Competition in the medical device products industry is rigorous with many companies having significant capital resources, large research laboratories andextensive distribution systems greater than the Company’s. Some of the Company’s major competitors are Medtronic, Anspach, Johnson & Johnson, IntegraLife Sciences, Inc., Söering, Stryker Corporation and Smith and Nephew. Regulatory Requirements The Company’s medical device products are subject to the regulatory requirements of the U.S. Food and Drug Administration (“FDA”) and otherinternational regulatory authorities. In the United States and other markets where the Company’s products are sold, the Company has the appropriatemarketing authorizations and complies with all applicable regulations including, without limitation, 21 USC Chapter 6, 21 CFR Part 807, 93/42 EEC and Health Canada SOR/98-282. In the US, Misonix products have 510(k) clearances. The Company also operates and maintains a Quality Management System which complies with the requirements of International Standards ISO 13485: 2012+ AC:2012, Health Canada CAN/CSA ISO 13485:2003, and US 21CFR Part 820 Quality System Regulation. This system encompasses the principle ofenhancing customer satisfaction through the effective application of the system, including processes for control, monitoring, and continual improvement inorder to assure the Company consistently meets or exceeds customer expectations and applicable statutory/regulatory requirements. 6 The Company is not aware of any regulatory situations, other than those disclosed in Item 3 herein, that would materially impact the Company, nor is theCompany aware of any pending legal action or new material breaches of the regulations to which it is subject. Trademarks, Patents, and Copyrights The Company holds 55 U.S. patents along with 12 in Europe, 9 in Japan and 14 in Canada and has multiple pending patent applications for its core productlines including ultrasonic and wound technologies, among other things. The Company believes that these patents provide it with a competitive marketadvantage. The Company also holds 13 trademarks protecting its Company and product names. The Company will continue to seek patent, trademark, and copyright protections as it deems advisable to protect the markets for its products and its R&Defforts. Backlog As of June 30, 2017, the Company’s backlog (firm orders that have not yet been shipped) was $397,660 as compared to $45,256 as of June 30, 2016. TheCompany does not typically have large recurring orders, but instead ships most of its products on a just in time basis, which results in low levels of backlog. Employees As of June 30, 2017, the Company employed a total of 92 full-time employees, including 32 in management and supervisory positions. The Companyconsiders its relationship with its employees to be good. Website Access Disclosure The Company’s Annual Reports on Form 10-K, Quarterly Reports on Form 10-Q and Current Reports on Form 8-K are available free of charge on theCompany’s website at www.misonix.com as soon as reasonably practicable after such material is electronically filed with or furnished to the SEC. Copies ofthe Company’s Annual Report will be made available to shareholders, free of charge, upon written request. Item 1A. Risk Factors. In addition to the other information contained in this Annual Report on Form 10-K (the “10-K”) and the exhibits hereto, the following risk factors should beconsidered carefully in evaluating our business. Our business, financial condition and/or results of operations could be materially adversely affected by anyof these risks. This section contains forward-looking statements. You should refer to the explanation of the qualifications and limitations on forward-lookingstatements set forth immediately prior to the beginning of Item 1 of the 10-K. Additional risks not presently known to us or that we currently deem immaterialmay also adversely affect our business, financial condition and/or results of operations. The following list sets forth many, but not all, of the factors that couldimpact the Company’s ability to achieve results discussed in any forward-looking statement. Investors should understand that it is not possible to predict oridentify all such factors and should not consider this list to be a complete statement of all potential risks and uncertainties. Risks Related to Our Business The termination of our former Chinese distributor will have an adverse effect on our sales revenue. For the fiscal years ended June 30, 2017, 2016 and 2015, our former Chinese distributor accounted for 0.2%, 6.4%, and 13.4% of our net sales, respectively.This distributor was our largest single customer during fiscal 2016 and fiscal 2015. We have ended our commercial relationship during the first quarter offiscal 2017 due to allegations of potential violation of laws (See Item 3 “Legal Proceedings”). The Company then engaged a replacement distributor duringthe third quarter of fiscal 2017. The termination of our prior distributor could continue to have an adverse effect on our net sales if sales from the new Chinesedistributor are less than the prior distributor. 7 We are subject to extensive medical device regulation which may impede or hinder the approval process for our products and, in some cases, may notultimately result in approval or may result in the recall or seizure of previously approved products. Our products, development activities and manufacturing processes are subject to extensive and rigorous regulation in the United States by the FDA pursuantto the Federal Food, Drug, and Cosmetic Act (the “FDC Act”), by comparable agencies in foreign countries, and by other regulatory agencies and governingbodies. Under the FDC Act, medical devices must receive FDA clearance or approval before they can be commercially marketed in the U.S. In addition, mostmajor markets for medical devices outside the U.S. require clearance, approval or compliance with certain standards before a product can be commerciallymarketed. The process of obtaining marketing approval or clearance from the FDA for new products, or with respect to enhancements or modifications toexisting products, could: ●take a significant amount of time; ●require the expenditure of substantial resources; ●involve rigorous pre-clinical and clinical testing; ●require changes to the products; and ●result in limitations on the proposed uses of the products. Marketing approvals or clearances are not the only risk. The FDA, and other regulatory bodies, also can require the withdrawal of an approved or clearedproduct from commercial distribution due to failure to comply with regulatory standards or the occurrence of unforeseen problems. As a medical device manufacturer, we are required to register with the FDA and are subject to periodic inspection by the FDA for compliance with the FDA’sQuality System Regulation requirements, which require manufacturers of medical devices to adhere to certain regulations, including testing, quality controland documentation procedures. In addition, FDA regulations require us to provide information to the FDA whenever there is evidence that reasonablysuggests that a medical device may have caused or contributed to a death or serious injury or, if a malfunction were to occur, could cause or contribute to adeath or serious injury. Compliance with applicable regulatory requirements is subject to continual review and is rigorously monitored through periodicinspections by the FDA. In the European Union and China, we are required to maintain certain ISO certifications in order to sell our products and mustundergo periodic inspections by notified bodies to obtain and maintain these certifications. Failure to meet regulatory quality standards could have amaterial adverse effect on our business, financial condition or results of operations. Consequently, there can be no assurance that we will receive the required clearances from the FDA or other regulatory bodies for new products ormodifications to existing products on a timely basis or that any FDA approval will not be subsequently withdrawn. Later discovery of previously unknownproblems with a product or manufacturer could result in fines, delays or suspensions of regulatory clearances, seizures or recalls of products, operatingrestrictions and/or criminal prosecution. The failure to receive product approval clearance on a timely basis, suspensions of regulatory clearances, seizures orrecalls of products or the withdrawal of product approval by the FDA or other regulatory bodies could have a material adverse effect on our business,financial condition or results of operations. 8 We may not be able to effectively protect our intellectual property rights. Patents and other proprietary rights are and will be essential to our business and our ability to compete effectively with other companies. We also rely upontrade secrets, know-how, continuing technological innovations, strategic alliances and licensing opportunities to develop, maintain and strengthen ourcompetitive position. We pursue a policy of generally obtaining patent protection in both the U.S. and abroad for patentable subject matter in our proprietarydevices and also attempt to review third-party patents and patent applications to the extent publicly available to develop an effective patent strategy, avoidinfringement of third-party patents, identify licensing opportunities and monitor the patent claims of others. We currently own numerous U.S. and foreignpatents. We also are party to various license agreements pursuant to which patent rights have been obtained or granted in consideration for cash or royaltypayments. No assurance can be made that any pending or future patent applications will result in issued patents, that any current or future patents issued to, orlicensed by, us will not be challenged or circumvented by our competitors, or that our patents will not be found invalid. We also operate in an industry that is susceptible to significant intellectual property litigation and, in recent years, it has been common for companies in themedical device field to aggressively challenge the patent rights of other companies in order to prevent the marketing of new devices. Intellectual propertylitigation is expensive, complex and lengthy and its outcome is difficult to predict. Future patent litigation may result in significant royalty or otherpayments or injunctions that can prevent the sale of products and may significantly divert the attention of our technical and management personnel. In addition, we may have to take legal action in the future to protect our patents, trade secrets or know-how or to assert our intellectual property rights againstclaimed infringement by others. Any legal action of that type could be costly and time consuming to us and no assurances can be made that any lawsuit willbe successful. The invalidation of key patents or proprietary rights that we own, or an unsuccessful outcome in lawsuits to protect our intellectual property, could have amaterial adverse effect on our business, financial condition or results of operations. In the event that our right to market any of our products is successfullychallenged, or if we fail to obtain a required license or are unable to design around a patent, our business, financial condition or results of operations could bematerially adversely affected. Future product liability claims and other litigation may adversely affect our business, reputation and ability to attract and retain customers. The design, manufacture and marketing of medical device products of the types that we produce entail an inherent risk of product liability claims. A numberof factors could result in an unsafe condition or injury to, or death of, a patient with respect to these or other products that we manufacture or sell, includingcomponent failures, manufacturing flaws, design defects or inadequate disclosure of product-related risks or product-related information. These factors couldresult in product liability claims, a recall of one or more of our products or a safety alert relating to one or more of our products. Product liability claims maybe brought by individuals or by groups seeking to represent a class. Anyone or any company can bring an action against Misonix, including private securities litigation and shareholder derivative suits, and adverselitigation results could affect our business. Our judicial system allows anyone, including shareholders, to bring a claim against the Company and force the Company to defend itself even if the claim isbaseless. The defense may or may not be covered by the Company’s insurance, the result of which could ultimately create a burden on the Companydependent upon the outcome. Litigation can be lengthy, expensive and disruptive to our operations, and results cannot be predicted with certainty. An adverse decision could result inmonetary damages or injunctive relief that could affect our financial condition or results of operations. On September 19, 2016, Richard Scalfani, an individual shareholder of Misonix, filed a lawsuit against the Company and its former CEO and CFO in the U.S.District Court for the Eastern District of New York, alleging violations of the federal securities laws. The complaint alleges that the Company’s stock pricewas artificially inflated between November 5, 2015 and September 14, 2016 as a result of alleged false and misleading statements in the Company’s securitiesfilings concerning the Company’s business, operations, and prospects and the Company’s internal control over financial reporting. Scalfani filed the actionseeking to represent a putative class of all persons (other than defendants, officers and directors of the Company, and their affiliates) who purchased publiclytraded Misonix securities between November 5, 2015 and September 14, 2016. Scalfani seeks an unspecified amount of damages for himself and for theputative class under the federal securities laws. On March 24, 2017, the Court appointed Scalfani and another individual Misonix shareholder, TraceyAngiuoli, as lead plaintiffs for purposes of pursuing the action on behalf of the putative class. The lead plaintiffs, on behalf of the putative class, and theCompany have reached a settlement in principle under which the Company would pay $500,000 to resolve the matter. That settlement is subject to approvalby the district court. The Company believes it has various legal and factual defenses to the allegations in the complaint, and intends to vigorously defend theaction if the settlement is not approved and finalized. 9 On April 5, 2017, the Company’s former distributor in China, Cicel, filed a lawsuit against the Company and certain officers and directors of the Company inthe United States District Court for the Eastern District of New York, alleging that the Company improperly terminated its contract with the former distributor.The complaint, which seeks various remedies, including compensatory and punitive damages, specific performance and preliminary and post judgmentinjunctive relief, asserts various causes of action, including breach of contract, unfair competition, tortious interference with contract, fraudulent inducement,and conversion. The Company believes it has various legal and factual defenses to the allegations in the complaint, and intends to vigorously defend theaction. The case is at its earliest stages; there has been no discovery and there is no trial date. On June 6, 2017, Irving Feldbaum, an individual shareholder of Misonix, filed a lawsuit in the U.S. District Court for the Eastern District of New York. Thecomplaint alleges claims against the Company’s board of directors, its former CEO and CFO, certain of its former directors, and the Company as a nominaldefendant for alleged violations of Section 14(a) of the Securities Exchange Act of 1934 (the “Exchange Act”) and state law claims for breach of fiduciaryduty, waste of corporate assets, and unjust enrichment. The complaint alleges that the Company incurred damages as a result of alleged false and misleadingstatements in the Company’s securities filings concerning the Company’s business, operations, and prospects and the Company’s internal control overfinancial reporting. The complaint also alleges that the Company’s February 4, 2016 Proxy Statement contained false and misleading statements regardingexecutive compensation. The complaint seeks the recovery of damages on behalf of the Company and the implementation of changes to corporategovernance procedures. On June 16, 2017, Michael Rubin, another individual shareholder of Misonix, filed a case alleging similar claims in the same districtcourt. The cases are at their earliest stages; there has been no discovery and there is no trial date. While the Company believes that these matters will becovered by its directors and officers liability insurance contract, the Company is not able either to estimate the amount of potential loss or potential recoveryit may recognize, if any, from these claims or to identify any changes in corporate governance procedures it may undertake, if any, as a result of these claims. Violation of anti-corruption laws could subject the Company to significant penalties which would materially affect our business and liquidity. We are required to comply with the Foreign Corrupt Practices Act (“FCPA”) and similar anti-corruption laws in other jurisdictions around the world where wedo business. Compliance with these laws has been subject to increasing focus and activity by regulatory authorities in recent years. Actions by ouremployees, or third-party intermediaries acting on our behalf, in violation of such laws, whether carried out in the United States or elsewhere in connectionwith the conduct of our business may expose us to liability for violations of the FCPA or other anti-corruption laws and accordingly may have a materialadverse effect on our reputation and our business, financial condition or results of operations. For several months, with the assistance of outside counsel, the Company has been conducting a voluntary investigation into the business practices of theindependent Chinese entity that previously distributed its products in China and the Company’s knowledge of those business practices, which may haveimplications under the FCPA, as well as into various internal controls issues identified during the investigation (the “Investigation”). On September 27, 2016 and September 28, 2016, the Company voluntarily contacted the Securities Exchange Commission (“SEC”) and the U.S. Departmentof Justice (“DOJ”), respectively, to advise both agencies of these potential issues. The Company has provided and will continue to provide documents andother information to the SEC and the DOJ, and is cooperating fully with these agencies in their ongoing investigations of these matters. 10 Although our Investigation is complete, additional issues or facts could arise which may expand the scope or severity of the potential violations. TheCompany could also receive additional requests from the DOJ or SEC, which may require further investigation. The Company has no current informationderived from the Investigation or otherwise to suggest that its previously reported financial statements and results are incorrect. At this stage, the Company is unable to predict what, if any, action the DOJ or the SEC may take or what, if any, penalties or remedial measures these agenciesmay seek. Nor can the Company predict the impact on the Company as a result of these matters, which may include the imposition of fines, civil and criminalpenalties, which are not currently estimable, as well as equitable remedies, including disgorgement of any profits earned from improper conduct andinjunctive relief, limitations on the Company’s conduct, and the imposition of a compliance monitor. The DOJ and the SEC periodically have based theamount of a penalty or disgorgement in connection with an FCPA action, at least in part, on the amount of profits that a company obtained from the businessin which the violations of the FCPA occurred. During its distributorship relationship with the prior Chinese distributor from 2010 through 2016, theCompany generated sales of approximately $8 million from the relationship. We cannot assure you that the DOJ and the SEC will not impose penalties basedon the profit derived from these sales. Further, the Company may suffer other civil penalties or adverse impacts, including lawsuits by private litigants in addition to the lawsuits that already havebeen filed, or investigations and fines imposed by local authorities. The investigative costs to date are approximately $2.5 million, of which approximately$2.4 million was charged to general and administrative expenses during the fiscal year ended June 30, 2017. As a result of the delayed filings of our Quarterly Reports on Form 10-Q for the fiscal period ended September 30, 2016 and December 31, 2016,respectively, and the Annual Report on Form 10-K for the fiscal year ended June 30, 2016 with the SEC, we are not currently eligible to use a registrationstatement on Form S-3 to register the offer and sale of securities, which may adversely affect our ability to raise future capital or complete acquisitions. We are not currently eligible to register the offer and sale of our securities using a registration statement on Form S-3 and we will not become eligible until wehave timely filed certain periodic reports required under the Exchange Act for 12 consecutive calendar months. There can be no assurance when we will meetthis requirement, which depends in part upon our ability to file our periodic reports on a timely basis in the future. Should we wish to register the offer andsale of our securities to the public before we are eligible to do so, on Form S-3, our transaction costs and the amount of time required to complete thetransaction could increase, making it more difficult to execute any such transaction successfully and potentially having an adverse effect on our financialcondition. Our future growth is dependent upon the development of new products and line extensions, which requires significant research and development, clinicaltrials and regulatory approvals, all of which are very expensive and time-consuming and may not result in a commercially viable product. In order to develop new products and improve current product offerings, we focus our research and development programs largely on the development ofnext-generation and novel technology offerings across multiple programs and opportunities. As a part of the regulatory process of obtaining marketing clearance from the FDA for new products, we conduct and participate in numerous clinical trialswith a variety of study designs, patient populations and trial endpoints. Unfavorable or inconsistent clinical data from existing or future clinical trialsconducted by us, by our competitors or by third parties, or the market’s perception of this clinical data, may adversely impact our ability to obtain productapprovals from the FDA, our position in, and share of, the markets in which we participate and our business, financial condition, results of operations or futureprospects. 11 New products may not be accepted by customers in the marketplace. We are now, and will continue to be, developing new products and introducing them into the market. There can be no assurance that any new product will beaccepted by the market. New products are sometimes introduced into the market in a prototype format and may need later revisions or design changes beforethey operate in a manner to be accepted in the market. As a result of the introduction of new products, there is some risk that revenue expectations may not bemet and in some cases the product may not achieve market acceptance. We face intense competition and may not be able to keep pace with the rapid technological changes in the medical device industry. The medical device product market is highly competitive. We encounter significant competition across our product lines and in each market in which ourproducts are sold from various medical device companies, most of which have greater financial and marketing resources than we do. Additionally, the medical device product market is characterized by extensive research and development and rapid technological change. Developments byother companies of new or improved products, processes or technology may make our products or proposed products obsolete or less competitive and maynegatively impact our revenues. In some cases foreign companies may attempt to copy our designs illegally. We are required to devote continued efforts andfinancial resources to develop or acquire scientifically advanced technologies and products, apply our technologies cost-effectively across product lines andmarkets, attract and retain skilled development personnel, obtain patent and other protection for our technology and products, obtain required regulatory andreimbursement approvals and successfully manufacture and market our products. Failure to develop new products or enhance existing products could have amaterial adverse effect on our business, financial condition or results of operations. Consolidation in the healthcare industry could lead to demands for price concessions or the exclusion of some suppliers from certain of our significantmarket segments. The cost of healthcare has risen significantly over the past decade and numerous initiatives and reforms initiated by legislators, regulators and third-partypayers to curb these costs have resulted in a consolidation trend in the healthcare industry, including hospitals. This in turn has resulted in greater pricingpressures and the exclusion of certain suppliers from important market segments as group purchasing organizations, independent delivery networks and largesingle accounts continue to consolidate purchasing decisions for some of our hospital customers. We expect that market demand, government regulation,third-party reimbursement policies and societal pressures will continue to change the worldwide healthcare industry, resulting in further businessconsolidations and alliances among our customers and competitors, which may reduce competition, exert further downward pressure on the prices of ourproducts and may adversely impact our business, financial condition or results of operations. We may experience disruption in supply due to our dependence on our suppliers to continue to ship product requirements and our inability to obtainsuppliers of certain components for our products. Our suppliers may encounter problems during manufacturing due to a variety of reasons, including failure to follow specific protocols and procedures, failureto comply with applicable regulations, equipment malfunctions, labor shortages or environmental factors. In addition, we purchase both raw materials used inour products and finished goods from various suppliers and may have to rely on a single source supplier for certain components of our products where thereare no alternatives are available. Although we anticipate that we have adequate sources of supply and/or inventory of these components to handle ourproduction needs for the foreseeable future, if we are unable to secure on a timely basis sufficient quantities of the materials we depend on to manufacture ourproducts, if we encounter delays or contractual or other difficulties in our relationships with these suppliers, or if we cannot find suppliers at an acceptablecost, then the manufacture of our products may be disrupted, which could increase our costs and have a material adverse effect on our business. If we fail to manage any expansion or acquisition, our business could be impaired. We may in the future acquire one or more technologies, products or companies that complement our business. We may not be able to effectively integratethese into our business and any such acquisition could bring additional risks, exposures and challenges to the Company. In addition, acquisitions may diluteour earnings per share, disrupt our ongoing business, distract our management and employees, increase our expenses, subject us to liabilities and increase ourrisk of litigation, all of which could harm our business. If we use cash to acquire technologies, products, or companies, such use may divert resourcesotherwise available for other purposes. If we use our common stock to acquire technologies, products, or companies, our shareholders may experiencesubstantial dilution. If we fail to manage any expansions or acquisition, our business could be impaired. 12 Our agreements and contracts entered into with partners and other third parties may not be successful. We signed in the past and may pursue in the future agreements and contracts with third parties to assist in our marketing, manufacturing, selling anddistribution efforts. We cannot assure you that any agreements or contracts entered into will be successful. The fluctuation of our quarterly results may adversely affect the trading price of our common stock. Our revenues and results of operations have in the past and will likely vary in the future from quarter to quarter due to a number of factors, many of which areoutside of our control and any of which may cause our stock price to fluctuate. You should not rely on quarter-to-quarter comparisons of our results ofoperations as an indication of our future performance. It is likely that in some future quarters, our results of operations may be below the expectations ofpublic market analysts and investors. In this event, the price of our common stock may fall. We may not be able to attract and retain additional key management, sales and marketing and technical personnel, or we may lose existing keymanagement, sales and marketing or technical personnel, which may delay our development and marketing efforts. We depend on a number of key management, sales and marketing and technical personnel. The loss of the services of one or more key employees could delaythe achievement of our development and marketing objectives. Our success will also depend on our ability to attract and retain additional highly qualifiedmanagement, sales and marketing and technical personnel to meet our growth goals. We face intense competition for qualified personnel, many of whom areoften subject to competing employment offers, and we do not know whether we will be able to attract and retain such personnel. Future changes in financial accounting standards or practices or existing taxation rules or practices may cause adverse or unexpected revenuefluctuations and affect our reported results of operations. A change in accounting standards or practices or a change in existing taxation rules or practices can have a significant effect on our reported results and mayeven affect our reporting of transactions completed before the change is effective. New accounting pronouncements and taxation rules and varyinginterpretations of accounting pronouncements and taxation practice have occurred and may occur in the future. Changes to existing rules or the questioningof current practices may adversely affect our reported financial results or the way we conduct our business. The Affordable Healthcare for America Act includes provisions that may adversely affect our business and results of operations, including an excise tax onthe sales of most medical devices. On March 21, 2010, the House of Representatives passed the Affordable Health Care for America Act, which President Obama signed into law on March 23,2010. With a new administration in place beginning in 2017, changes may be made to the Affordable Health Care Act, or it may be repealed and replaced.The potential impact of these events may adversely affect our business and results of operations. The medical device tax has been established, but in thefuture the government may decide to increase the tax rate. The impact of the recent change in Presidential administration has yet to be determined. We are experiencing greater scrutiny and regulation by governmental authorities, which may lead to greater regulation in the future. Our medical devices and our business activities are subject to rigorous regulation, including by the FDA, the DOJ and numerous other federal, state andforeign governmental authorities. These authorities and members of Congress have been increasing their scrutiny of our industry. Certain state governmentsand the federal government have enacted legislation aimed at increasing transparency of our interactions with health care providers. As a result, we arerequired by law to disclose payments and other transfers of value to health care providers licensed by certain states and, starting with payments or othertransfers of value made on or after August 1, 2013, to all U.S. physicians and U.S. teaching hospitals at the federal level. Any failure to comply with theselegal and regulatory requirements could impact our business. In addition, we may continue to devote substantial additional time and financial resources tofurther develop and implement policies, systems, and processes to comply with enhanced legal and regulatory requirements, which may also impact ourbusiness. We anticipate that governmental authorities will continue to scrutinize our industry closely, and that additional regulation may increasecompliance and legal costs, exposure to litigation, and other adverse effects on our operations. 13 Risk of reprocessing disposables. In some jurisdictions around the world, culture and practice encourages reuse of disposable products when the product is clearly labeled for single use. Suchreuse may expose us to liability in these jurisdictions. Item 1B. Unresolved Staff Comments. None. Item 2. Properties. The Company occupies approximately 34,400 square feet at 1938 New Highway, Farmingdale, New York pursuant to a lease expiring on June 30, 2018. TheCompany pays rent of approximately $26,000 a month, which includes a pro rata share of real estate taxes, water, sewer and other charges which are assessedon the leased premises or the land upon which the leased premises are situated. The Company believes that the leased facilities are adequate for its presentneeds. Item 3. Legal Proceedings. Former Chinese Distributor For several months, with the assistance of outside counsel, the Company has been conducting the Investigation into the business practices of the independentChinese entity that previously distributed its products in China and the Company’s knowledge of those business practices, which may have implicationsunder the FCPA, as well as into various internal controls issues identified during the Investigation. On September 27, 2016 and September 28, 2016, the Company voluntarily contacted the SEC and the DOJ, respectively, to advise both agencies of thesepotential issues. The Company has provided and will continue to provide documents and other information to the SEC and the DOJ, and is cooperating fullywith these agencies in their ongoing investigations of these matters. Although our Investigation is complete, additional issues or facts could arise which may expand the scope or severity of the potential violations. TheCompany has no current information derived from the Investigation or otherwise to suggest that its previously reported financial statements and results areincorrect. At this stage, the Company is unable to predict what, if any, action the DOJ or the SEC may take or what, if any, penalties or remedial measures these agenciesmay seek. Nor can the Company predict the impact on the Company as a result of these matters, which may include the imposition of fines, civil and criminalpenalties, which are not currently estimable, as well as equitable remedies, including disgorgement of any profits earned from improper conduct andinjunctive relief, limitations on the Company’s conduct, and the imposition of a compliance monitor. The DOJ and the SEC periodically have based theamount of a penalty or disgorgement in connection with an FCPA action, at least in part, on the amount of profits that a company obtained from the businessin which the violations of the FCPA occurred. During its distributorship relationship with the prior Chinese distributor from 2010 through 2016, theCompany generated sales of approximately $8 million from the relationship. 14 Further, the Company may suffer other civil penalties or adverse impacts, including lawsuits by private litigants in addition to the lawsuits that already havebeen filed, or investigations and fines imposed by local authorities. The investigative costs to date are approximately $2.5 million, of which approximately$2.4 million was charged to general and administrative expenses during the fiscal year ended June 30, 2017. Class Action Securities Litigation On September 19, 2016, Richard Scalfani, an individual shareholder of Misonix, filed a lawsuit against the Company and its former CEO and CFO in the U.S.District Court for the Eastern District of New York, alleging violations of the federal securities laws. The complaint alleges that the Company’s stock pricewas artificially inflated between November 5, 2015 and September 14, 2016 as a result of alleged false and misleading statements in the Company’s securitiesfilings concerning the Company’s business, operations, and prospects and the Company’s internal control over financial reporting. Scalfani filed the actionseeking to represent a putative class of all persons (other than defendants, officers and directors of the Company, and their affiliates) who purchased publiclytraded Misonix securities between November 5, 2015 and September 14, 2016. Scalfani seeks an unspecified amount of damages for himself and for theputative class under the federal securities laws. On March 24, 2017, the Court appointed Scalfani and another individual Misonix shareholder, Tracey Angiuoli, as lead plaintiffs for purposes of pursuingthe action on behalf of the putative class. The lead plaintiffs, on behalf of the putative class, and the Company have reached a settlement in principle underwhich the Company would pay $500,000 to resolve the matter. That settlement is subject to approval by the district court. The Company believes it hasvarious legal and factual defenses to the allegations in the complaint, and intends to vigorously defend the action if the settlement is not approved andfinalized. Stockholder Derivative LitigationOn June 6, 2017, Irving Feldbaum, an individual shareholder of Misonix, filed a lawsuit in the U.S. District Court for the Eastern District of New York. Thecomplaint alleges claims against the Company’s board of directors, its former CEO and CFO, certain of its former directors, and the Company as a nominaldefendant for alleged violations of Section 14(a) of the Securities Exchange Act of 1934 and state law claims for breach of fiduciary duty, waste of corporateassets, and unjust enrichment. The complaint alleges that the Company incurred damages as a result of alleged false and misleading statements in theCompany’s securities filings concerning the Company’s business, operations, and prospects and the Company’s internal control over financial reporting. Thecomplaint also alleges that the Company’s February 4, 2016 Proxy Statement contained false and misleading statements regarding executive compensation.The complaint seeks the recovery of damages on behalf of the Company and the implementation of changes to corporate governance procedures. On June 16,2017, Michael Rubin, another individual shareholder of Misonix, filed a case alleging similar claims in the same district court. The cases are at their earlieststages; there has been no discovery and there is no trial date. The Company is not able either to estimate the amount of potential loss or potential recovery itmay recognize, if any, from these claims or to identify any changes in corporate governance procedures it may undertake, if any, as a result of these claims. Former Chinese Distributor - Litigation On April 5, 2017, the Company’s former distributor in China, Cicel (Beijing) Science & Technology Co., Ltd., filed a lawsuit against the Company andcertain officers and directors of the Company in the United States District Court for the Eastern District of New York, alleging that the Company improperlyterminated its contract with the former distributor. The complaint, which seeks various remedies, including compensatory and punitive damages, specificperformance and preliminary and post judgment injunctive relief, asserts various causes of action, including breach of contract, unfair competition, tortiousinterference with contract, fraudulent inducement, and conversion. The Company believes it has various legal and factual defenses to the allegations in thecomplaint, and intends to vigorously defend the action. The case is at its earliest stages; there has been no discovery and there is no trial date. Item 4. Mine Safety Disclosures. Not applicable. 15 PART II Item 5. Market for Registrant’s Common Equity, Related Stockholder Matters and Issuer Purchases of Equity Securities. The Company’s common stock, $.01 par value (“Common Stock”), is listed on the Nasdaq Global Market under the symbol “MSON”. The following table sets forth the high and low sales prices for the Common Stock during the periods indicated as reported by the Nasdaq Global Market: High Low Fiscal 2017: First Quarter $7.15 $4.95 Second Quarter 11.20 4.85 Third Quarter 12.00 9.05 Fourth Quarter 11.80 9.35 High Low Fiscal 2016: First Quarter $12.00 $8.20 Second Quarter 11.99 8.41 Third Quarter 9.41 5.64 Fourth Quarter 6.25 3.83 As of June 30, 2017, the Company had 9,357,166 shares of Common Stock outstanding and 60 shareholders of record. This amount does not take intoaccount shareholders whose shares are held in “street name” by brokerage houses or other intermediaries. The Company has not paid any cash dividends since its inception. The Company does not intend to pay any cash dividends in the foreseeable future, butintends to retain all earnings, if any, for use in its business operations. Share Performance Graph The following graph compares the cumulative total return on the Company’s Common Stock during the last five fiscal years with the NASDAQ Total U.S.and Foreign Return Index and the NASDAQ Medical Devices, Instruments and Supplies Index during the same period. The graph shows the value, at the endof each of the last five fiscal years, of $100 invested in the Common Stock or the indices on June 30, 2012. The graph depicts the change in value of theCompany’s Common Stock relative to the noted indices as of the end of each fiscal year and not for any interim period. Historical stock price performance isnot necessarily indicative of future stock price performance. 2013 2014 2015 2016 2017 MISONIX, INC. 100 132 186 101 187 NASDAQ Composite Total Return 100 131 150 147 189 NASDAQ Medical Equipment Index 100 130 153 187 211 16 Item 6. Selected Financial Data. The following selected consolidated financial data should be read in conjunction with Item 7 “Management’s Discussion and Analysis of FinancialCondition and Results of Operations” and our consolidated financial statements and the related notes appearing in Item 8 “Financial Statements andSupplementary Data” of this 10-K. The consolidated statements of income data for the years ended June 30, 2015, 2016 and 2017 and the consolidated balance sheet data as of June 30, 2016and 2017 are derived from our audited consolidated financial statements appearing in Item 8 of this 10-K. The consolidated statements of income data for theyears ended June 30, 2013 and 2014 and the consolidated balance sheet data as of June 30, 2013, 2014 and 2015 are derived from our audited consolidatedfinancial statements that are not included in the 10-K. The historical results are not necessarily indicative of the results to be expected in any future period. Selected income statement data: For the Year Ended June 30, 2017 2016 2015 2014 2013 Net sales $27,269,963 $23,113,194 $22,204,578 $17,060,435 $14,827,226 Net (loss)/income from continuing operations (1,842,804) (1,329,077) 5,304,056 1,126,580 (2,846,747) Net (loss)/income per share from continuingoperations - Basic $(0.22) $(0.17) $0.70 $0.15 $(0.40) Net (loss)/income per share from continuingoperations - Diluted $(0.22) $(0.17) $0.66 $0.15 $(0.40) Selected balance sheet data: June 30, 2017 2016 2015 2014 2013 Total assets $33,369,649 $27,732,731 $26,454,248 $19,527,869 $17,359,927 Total long term liabilities $13,087 $31,685 $20,395 $67,932 $96,745 Total shareholders’ equity $28,139,842 $24,401,290 $23,754,345 $16,352,364 $13,777,220 Item 7. Management’s Discussion and Analysis of Financial Condition and Results of Operations. Misonix designs, manufactures, develops and markets therapeutic ultrasonic devices. These products are used for precise bone sculpting, removal of soft andhard tumors, and tissue debridement, orthopedic surgery, plastic surgery, and wound and burn care. In the United States, the Company sells its productsthrough a network of commissioned agents assisted by company personnel. Outside of the United States, the Company generally sells to distributors whothen resell the product to hospitals. The Company operates as one business segment. 17 In the United States, the Company is taking a more aggressive approach to taking market share, expanding the market and increasing its share of recurringdisposable revenue by using a consignment model, whereby the Company will consign the equipment (which is defined as a generator, hand units andaccessories) (the “Equipment”) and sell to customers higher margin disposable, single use items (the “Consumables”) on a recurring basis. Title remains withthe Company with respect to consigned Equipment, which is depreciated and charged to selling expenses over a five year period beginning in fiscal 2017,and a three year period in fiscal 2016. Outside of the United States, the Company has principally not yet adopted a consignment model. The Company’soverall goal is to increase the utilization rate of Equipment which will increase the total number of procedures and maximize the sale of Consumables to ourcustomers, with the goal of becoming the standard of care in the various segments we focus on. Results of Operations The following discussion and analysis provides information which the Company’s management believes is relevant to an assessment and understanding ofthe Company’s results of operations and financial condition. This discussion should be read in conjunction with the consolidated financial statements andnotes thereto appearing elsewhere herein. Unless otherwise specified, this discussion relates solely to the Company’s continuing operations. All of the Company’s sales have been derived from the sale of medical device products, which include manufacture and distribution of ultrasonic medicaldevice products. Fiscal years ended June 30, 2017, 2016 and 2015 Our sales by category for the three years ended June 30, 2017 are as follows: Net Change % For the Year Ended June 30, Year Ended June 30, 2017 2016 2015 2017 2016 Total Consumables $20,328,676 $16,091,651 $12,833,377 26.3% 25.4%Equipment 6,941,287 7,021,543 9,371,201 (1.1)% (25.1)%Total $27,269,963 $23,113,194 $22,204,578 18.0% 4.1% Domestic: Consumables $14,866,772 $11,277,449 $8,449,215 31.8% 33.5%Equipment 1,593,999 1,809,357 2,348,705 (11.9)% (23.0)%Total $16,460,771 $13,086,806 $10,797,920 25.8% 21.2% International: Consumables $5,461,904 $4,814,202 $4,384,162 13.5% 9.8%Equipment 5,347,288 5,212,186 7,022,496 2.6% (25.8)%Total $10,809,192 $10,026,388 $11,406,658 7.8% (12.1)% Fiscal years ended June 30, 2017 and 2016 Net sales Net sales increased 18.0% or $4,156,769 to $27,269,963 in fiscal 2017 from $23,113,194 in fiscal 2016 principally due to stronger demand for theCompany’s products domestically, and partially from stronger international sales. BoneScapel product revenue increased $4,178,377, or 32.8% from fiscal2016. Consumables revenue increased by 26.3% to $20,328,676 for the year ended June 30, 2017 compared with $16,091,651 in the prior year. Equipmentsales declined by 1.1% to $6,941,287 compared with $7,021,543 in the prior year. Domestic sales increased to 60.4% of revenue in fiscal 2017, from 56.6%in fiscal 2016. 18 Gross profitGross profit was 69.9% in fiscal 2017, an increase of 2.8% from 67.1% in fiscal 2016. The increase resulted from a stronger mix of Consumables revenuewhich carries a higher gross profit margin than Equipment revenue. Selling expensesSelling expenses increased by $1,587,946, or 15.7% to $14,220,907 in fiscal 2017 from $12,632,961 in fiscal 2016. The expense increase is related toincreased commissions of approximately $1.4 million on higher sales of $4.2 million. General and administrative expensesGeneral and administrative expenses increased $2,765,690 to $9,565,206 in fiscal 2017 from $6,829,516 in fiscal 2016. The increase resulted principallyfrom increased professional fees of approximately $2.4 million relating to the Investigation, and an additional $442,000 of other professional fees. TheCompany also paid severance for its former CEO during the current year of approximately $335,000. This increase in expenses was partially offset by areduction in non-cash stock compensation expense of $805,000, which includes a reversal of stock compensation previously recognized with respect to theCompany’s prior CEO relating to unvested stock options which were terminated. The Company also recognized $484,000 of non-cash compensation expenserelating to the restricted stock awards granted to the Company’s new CEO in December 2016. Research and development expensesResearch and development expenses were $1,837,497 for fiscal 2017, approximately the same as fiscal 2016 expenses of $1,839,479. Other incomeOther income decreased $191,486 to $3,735,474 in fiscal 2017 from $3,926,960 in fiscal 2016. The decrease is related to lower royalty income from MMIT.This royalty agreement expired in August 2017. Income taxesIn fiscal 2017 the income tax benefit for continuing operations had an effective tax rate of 35.7% as compared to an effective rate of 30.1% in fiscal 2016.Prior to June 30, 2014 and through March 31, 2015, the Company had a full valuation allowance recorded against deferred tax assets. The primary factorsaffecting the fiscal 2017 effective tax rate were non-deductible expenses, stock compensation , tax credits and state income taxes. The primary factorsaffecting the fiscal 2016 effective tax rate were non-deductible expenses, deferred tax adjustments and state income taxes. As of the year ended June 30,2015, the Company reduced the valuation allowance by $5,503,417. The change in the valuation allowance includes a $1,499,297 write-off of deferred taxassets against its corresponding valuation allowance. The write-off primarily pertains to a loss in tax benefit for net operating losses subject to limitationunder federal tax law that precludes its utilization. In addition, during the fourth quarter of fiscal 2015, based on our consideration of all available positiveand negative evidence including achieving cumulative profitable operating performance over the past three years and our positive outlook for taxableincome in the future, the Company reevaluated its deferred tax asset. Based upon the guidance under ASC 740, we concluded that it was more likely than notthat the Company would realize the benefit of such deferred tax assets. The portion of the valuation allowance release attributable to income in future yearsresulted in the recognition of a tax benefit of $2,892,000 in continuing operations in the fourth quarter of fiscal 2015. The deferred tax asset will be realizedagainst future income tax expense that would be payable in the absence of the net operating loss carryforwards. The Company still maintains a full valuationallowance on all foreign net operating losses in the amount of $628,730. Fiscal years ended June 30, 2016 and 2015 Net salesNet sales increased $908,616, or 4.1%, to $23,113,194 in fiscal 2016 from $22,204,578 in fiscal 2015 in part due to stronger demand for the Company’sproducts domestically offset by weaker international Equipment sales. Consumables revenue increased by 25.4% to $16,091,651 for the year ended June 30,2016 compared with $12,833,377 in the prior year. Equipment sales declined by 25.1% to $7,021,543 compared with $9,371,201 in the prior year. Thedecline resulted from weaker international sales, principally in China, where the Company ceased shipments in the fourth quarter of fiscal 2016. 19 Gross profitGross profit was 67.1% in fiscal 2016, roughly flat with fiscal 2015, which was 67.2%. Selling expensesSelling expenses increased $3,570,266 to $12,632,961 in fiscal 2016 from $9,062,695 in fiscal 2015. The Company continues to invest in sales andmarketing in order to gain market share. The Company’s strategy to leverage its existing distributor network with product specialists domestically resulted inpart in domestic sales growing by 21.2% during the 2016 fiscal year. The expense increase is related to higher salary expenses of $1,140,737 due to increasedhead count, higher commissions of $798,432 from sales programs to increase the number of consigned units domestically, higher travel expenses of$349,701, higher advertising expenses of $344,322, higher depreciation expenses of $318,472 due to the increased consigned units, higher employee benefitexpenses of $154,175 due to increased head count, higher training expenses of $57,733, higher freight-out expenses of $54,906 and higher other expenses of$14,912. General and administrative expensesGeneral and administrative expenses increased $845,893 to $6,829,516 in fiscal 2016 from $5,983,623 in fiscal 2015. The increase is due to higher non-cashcompensation expenses of $522,393 due to the issuance of stock options, higher accounting expenses of $497,932 relating in part to the Company becomingan accelerated filer, higher insurance expenses of $175,584, higher salary expenses of $147,119 and higher depreciation expenses of $39,937. Research and development expensesResearch and development expenses increased $246,556 to $1,839,479 in fiscal 2016 from $1,592,923 in fiscal 2015. The increase is due generally to higherproduct development expenses. Other incomeOther income decreased $307,403 to $3,926,960 in fiscal 2016 from $4,234,363 in fiscal 2015. The decrease is related to lower royalty income from MMIT.This royalty agreement expired in August 2017. Income taxesIn fiscal 2016 the income tax benefit for continuing operations had an effective tax rate of 30.1% as compared to an effective rate of 110.5% in fiscal 2015.Prior to June 30, 2014 and through March 31, 2015, the Company had a full valuation allowance recorded against deferred tax assets. The primary factorsaffecting the fiscal 2016 effective tax rate were non-deductible expenses, deferred tax adjustments and state income taxes. As of the year ended June 30,2015, the Company reduced the valuation allowance by $5,503,417. The change in the valuation allowance includes a $1,499,297 write-off of deferred taxassets against its corresponding valuation allowance. The write-off primarily pertains to a loss in tax benefit for net operating losses subject to limitationunder federal tax law that precludes its utilization. In addition, during the fourth quarter of fiscal 2015, based on our consideration of all available positiveand negative evidence including achieving cumulative profitable operating performance over the past three years and our positive outlook for taxableincome in the future, the Company reevaluated its deferred tax asset. Based upon the guidance under ASC 740, we concluded that it was more likely than notthat the Company would realize the benefit of such deferred tax assets. The portion of the valuation allowance release attributable to income in future yearsresulted in the recognition of a tax benefit of $2,892,000 in continuing operations in the fourth quarter of fiscal 2015. The deferred tax asset will be realizedagainst future income tax expense that would be payable in the absence of the net operating loss carryforwards. The Company still maintains a full valuationallowance on all foreign net operating losses in the amount of $628,730. 20 Discontinued operations The following represents the results of the Laboratory and Forensic Safety Products business along with legal and other expenses associated with LabcaireSystems Limited and Misonix HIFU Technologies Limited which are included in discontinued operations: For the years ended June 30, 2017 2016 2015 Revenues $— $— $18,242 Income from discontinued operations, before tax $— $— $18,242 Gain on sale of discontinued operations 250,000 250,000 250,000 Income tax benefit/(expense) (88,375) (93,069) (1,127)Net income from discontinued operations, net of tax $161,625 $156,931 $267,115 Liquidity and Capital Resources Working capital at June 30, 2017 was $17,394,427 million. For fiscal 2017, cash used in operations was $1,272,658, mainly due to the Company’s net loss of$1,681,179 and an increase in accounts receivable of $1,263,962 and inventory of $873,136, offset by $2,152,983 of non-cash depreciation expense andnon-cash compensation. Cash used in investing activities was $714,815, primarily consisting of the purchase of property, plant and equipment along with filing for additionalpatents. Cash provided by financing activities was $4,333,592 for fiscal 2017. On October 25, 2016, the Company sold 761,469 shares of Common Stock in a privateplacement to Stavros G. Vizirgianakis, a director of the Company and its current Chief Executive Officer, at a price per share of $5.253, representing totalcash proceeds to the Company of approximately $4.0 million. In addition, the Company recognized $333,592 of stock option exercises. As of June, 2017, the Company had a cash balance of approximately $11,557,071 and believes it has sufficient cash to finance operations for at least the next12 months following the issuance date of the financial statements included herein. Relating to the internal investigation described herein, the Company has incurred approximately $2.5 million in investigative costs and is expected to incuradditional costs until the matter is fully resolved. Further, the Company could be subject to fines or penalties related to potential violations of the FCPA. The Company has been receiving an annual royalty from MMIT which has averaged $3.7 million per year over the last three fiscal years. This royalty endedin August 2017. Commitments The Company has commitments under operating leases that will be funded from operating sources. At June 30, 2017, the Company’s contractual cashobligations and commitments relating to operating leases and other purchase commitments are as follows: Less than After Commitment 1 year 1-3 years 4-5 years 5 years Total Operating leases $353,659 $21,812 $21,812 $9,225 $406,508 Purchase commitments 2,859,718 — — — 2,859,718 $3,213,377 $21,812 $21,812 $9,225 $3,266,226 Off-Balance Sheet Arrangements The Company has no off-balance sheet arrangements that have or are reasonably likely to have a current or future effect on the Company’s financialcondition, changes in financial condition, revenues or expenses, results of operations, liquidity, capital expenditures or capital resources that are material tothe Company. 21 Other In the opinion of management, inflation has not had a material effect on the operations of the Company. Critical Accounting Policies and Use of Estimates Our discussion and analysis of financial condition and results of operations is based upon our consolidated financial statements, which have been prepared inaccordance with accounting principles generally accepted in the United States of America. The preparation of these financial statements requires us to makeestimates and assumptions that affect the reported amounts of assets and liabilities, the disclosure of contingent liabilities, and the reported amounts ofrevenues and expenses. Significant estimates affecting amounts reported or disclosed in the consolidated financial statements include net realizable value ofinventories, valuation of intangible assets including amortization periods for acquired intangible assets, estimates of projected cash flows and discount ratesused to value intangible assets and test goodwill and intangible assets for impairment, computation of valuation allowances recorded against deferred taxassets, and valuation of stock-based compensation. These estimates are based on historical experience and on various other assumptions that are believed tobe reasonable under the current circumstances. Actual results could differ from these estimates. We believe that the following accounting policies, which form the basis for developing these estimates, are those that are most critical to the presentation ofour consolidated financial statements and require the more difficult subjective and complex judgments. Inventories Inventories, consisting of purchased materials, direct labor and manufacturing overhead, are stated at the lower of cost (determined by the first-in, first-outmethod) or market. At each balance sheet date, we evaluate ending inventories for excess quantities and obsolescence. Our evaluation includes an analysis ofhistorical sales levels by product, projections of future demand by product, the risk of technological or competitive obsolescence for our products, generalmarket conditions, and the feasibility of reworking or using excess or obsolete products or components in the production or assembly of other products thatare not obsolete or for which we do not have excess quantities in inventory. To the extent that we determine there are excess or obsolete quantities orquantities on hand, we adjust their carrying value to estimated net realizable value. If future demand or market conditions are lower than our projections, or ifwe are unable to rework excess or obsolete quantities into other products, we may record further adjustments to the carrying value of inventory through acharge to cost of product revenues in the period the revision is made. Goodwill The excess of the cost over the fair value of net assets of acquired businesses is recorded as goodwill. Goodwill is not subject to amortization, but is reviewedfor impairment at the reporting unit level annually, or more frequently if impairment indicators arise. Our assessment of the recoverability of goodwill isbased upon a comparison of the carrying value of goodwill with its estimated fair value and the value of the Company at the measurement date. Application of these impairment tests requires significant judgments, including estimation of cash flows, which is dependent on internal forecasts, estimationof the long term rate of growth for our business, the useful lives over which cash flows will occur and determination of our weighted average cost of capital.We primarily utilize a discontinued cash flow model in determining the fair value which consists of Level 3 inputs. Changes in the projected cash flows anddiscount rate estimates and assumptions underlying the valuation of goodwill could materially affect the determination of fair value at acquisition or duringsubsequent periods when tested for impairment. Income Taxes The Company assesses whether a valuation allowance should be established against its deferred tax assets based on consideration of all available evidence,both positive and negative, using a more likely than not standard. This assessment considers, among other matters, the nature, frequency and severity ofrecent losses; a forecast of future profitability; the duration of statutory carryback and carryforward periods; the Company’s experience with tax attributesexpiring unused; and tax planning alternatives. The likelihood that the deferred tax asset balance will be recovered from future taxable income is assessed atleast quarterly, and the valuation allowance, if any, is adjusted accordingly. 22 Loss Contingencies We are subject to claims and lawsuits in the ordinary course of our business, including claims by employees or former employees, with respect to our productsand involving commercial disputes, or shareholder actions. We accrue for loss contingencies when it is deemed probable that a loss has been incurred andthat loss is estimable. The amounts accrued are based on the full amount of the estimated loss before considering insurance proceeds, if applicable, and do notinclude an estimate for legal fees expected to be incurred in connection with the loss contingency. Other than $250,000 accrued for our ongoing class actionlitigation, our financial statements do not reflect any material amounts related to possible unfavorable outcomes of claims and lawsuits to which we arecurrently a party because we currently believe that such claims and lawsuits are not expected, individually or in the aggregate, to result in a material adverseeffect on our financial condition. However, it is possible that these contingencies could materially affect our results of operations, financial position and cashflows in a particular period if we change our assessment of the likely outcome of these matters. Relating to the FCPA matter described in Part I – Item 3 above,the Company has incurred approximately $2.5 million in investigative costs, of which approximately $2.4 million was charged to general and administrativeexpenses during the fiscal year ended June 30, 2017, and is expected to incur additional costs until the matter is fully resolved. Further, the Company couldbe subject to fines or penalties related to potential violations of the FCPA. Stock-Based Compensation We recognize compensation expense associated with the issuance of equity instruments to employees for their services. Based on the type of equityinstrument, the fair value is estimated on the date of grant using the Black-Scholes option valuation model, and is being expensed in the financial statementsover the service period and is recorded in general and administrative expenses. The input assumptions used in determining fair value are the expected life,expected volatility, risk-free rate and expected dividend yield. On December 15, 2016, we issued 400,000 shares of restricted stock to our Chief Executive Officer. These awards vest over a period of up to five years,subject to meeting certain service, performance and market conditions. We valued these awards using a Monte Carlo valuation model, which required the useof various estimates in arriving at the valuation of the awards. The valuation included the estimate of the probability of achieving the performance criteria,which included minimum levels of Company stock price and revenue. If the stock price and performance conditions are not met, some or all of these awardswill not vest and compensation cost recorded, if any, could be reversed. Recently Issued and Adopted Accounting Standards In May 2014, the Financial Accounting Standards Board (the “FASB”) issued guidance on revenue from contracts with customers. The underlying principleis that an entity will recognize revenue to depict the transfer of goods or services to customers at an amount that the entity expects to be entitled to inexchange for those goods or services. The guidance provides a five-step analysis of transactions to determine when and how revenue is recognized. Othermajor provisions include capitalization of certain contract costs, consideration of time value of money in the transaction price, and allowing estimates ofvariable consideration to be recognized before contingencies are resolved, in certain circumstances. The guidance also requires enhanced disclosuresregarding the nature, amount, timing and uncertainty of revenue and cash flows arising from an entity’s contracts with customers. This guidance permits theuse of either the retrospective or cumulative effect transition method and is effective for the Company beginning in 2019; early adoption is permittedbeginning in 2018. We have not yet selected a transition method and are currently evaluating the impact of the guidance on the Company’s financialcondition, results of operations and related disclosures. The FASB has also issued the following additional guidance clarifying certain issues on revenue fromcontracts with customers: Revenue from Contracts with Customers - Narrow-Scope Improvements and Practical Expedients and Revenue from Contracts withCustomers - Identifying Performance Obligations and Licensing. The Company is currently in the early stages of evaluating this guidance to determine theimpact it will have on its financial statements. The Company expects that its evaluation should be complete in early 2018. 23 In August 2014, the FASB issued guidance on management’s responsibility in evaluating whether there is substantial doubt about a company’s ability tocontinue as a going concern and related footnote disclosures. Management will be required to evaluate, at each reporting period, whether there are conditionsor events that raise substantial doubt about a company’s ability to continue as a going concern within one year from the date the financial statements areissued. This guidance is effective prospectively for annual and interim reporting periods ending after 2016; implementation of this guidance did not result amaterial effect on the Company’s financial condition or results of operations. In July 2015, the FASB issued ASU 2015-11, Simplifying the Measurement of Inventory. ASU 2015-11 applies to inventory that is measured using first-in,first-out (FIFO) or average cost. An entity should measure inventory within the scope of ASU 2015-11 at the lower of cost and net realizable value. Netrealizable value is the estimated selling prices in the ordinary course of business, less reasonably predictable costs of completion, disposal and transportation.The amendments in ASU 2015-11 more closely align the measurement of inventory in US GAAP with the measurement of inventory in InternationalFinancial Reporting Standards (IFRS). ASU 2015-11 is effective for fiscal years beginning after December 15, 2016. The Company does not expect theadoption of ASU 2015-11 to have a material impact on its consolidated financial statements. In November 2015, the FASB issued ASU 2015-17 “Balance Sheet Classification of Deferred Taxes (Topic 740)”. The amendments in this ASU requiredeferred tax liabilities and assets be classified as noncurrent in a classified statement of financial position. The amendments eliminate the guidance in Topic740 that requires an entity to separate deferred tax liabilities and assets into a current amount and a noncurrent amount in a classified statement of financialposition. The Company adopted ASU 2015-17 as of March 31, 2016 on a prospective basis in order to simplify the balance sheet classification of deferredtaxes. In February 2016, the FASB issued guidance on lease accounting requiring lessees to recognize a right-of-use asset and a lease liability for long-term leases.The liability will be equal to the present value of lease payments. This guidance must be applied using a modified retrospective transition approach to allannual and interim periods presented and is effective for the Company beginning in fiscal 2019. The Company is currently in the early stages of evaluatingthis guidance to determine the impact it will have on its financial statements. In March 2016, the FASB issued guidance on simplifying several aspects of accounting for share-based payment award transactions, including income taxconsequences, classification of awards as either equity or liabilities, and classification on the statement of cash flows. This guidance requires a mix ofprospective, modified retrospective, and retrospective transition to all annual and interim periods presented and is effective for the Company beginning infiscal 2018. This guidance was adopted by the Company on July 1, 2017. This guidance will be adopted by the Company on July 1, 2017 and managementexpects this to result in an increase in the Company’s deferred tax asset of approximately $2.5 million. In August 2016, the FASB issued guidance on the Statement of Cash Flows Classification of certain cash receipts and cash payments (a consensus of theEmerging Issues Task Force). This guidance addresses the following eight specific cash flow issues: Debt prepayment or debt extinguishment costs;settlement of zero-coupon debt instruments or other debt instruments with coupon interest rates that are insignificant in relation to the effective interest rateof the borrowing; contingent consideration payments made after a business combination; proceeds from the settlement of insurance claims; proceeds from thesettlement of corporate-owned life insurance policies (including bank-owned life insurance policies); distributions received from equity method investees;beneficial interests in securitization transactions; and separately identifiable cash flows and application of the predominance principle. This guidance will beeffective for the Company beginning in fiscal 2019. The Company is currently in the early stages of evaluating this guidance to determine the impact it willhave on its financial statements. In January 2017, the Financial Accounting Standards Board (the “FASB”) issued ASU No. 2017-04, Simplifying the Test for Goodwill Impairment. Under thenew standard, goodwill impairment would be measured as the amount by which a reporting unit’s carrying value exceeds its fair value, not to exceed thecarrying value of goodwill. This ASU eliminates existing guidance that requires an entity to determine goodwill impairment by calculating the implied fairvalue of goodwill by hypothetically assigning the fair value of a reporting unit to all of its assets and liabilities as if that reporting unit had been acquired ina business combination. This update is effective for annual periods beginning after December 15, 2019, and interim periods within those periods. Earlyadoption is permitted for interim or annual goodwill impairment tests performed on testing dates after January 1, 2017. The Company is applying thisguidance to applicable impairment tests after January 1, 2017. 24 In January 2017, the FASB issued ASU No. 2017-01, Business Combinations: Clarifying the Definition of a Business (“ASU 2017-01”). ASU 2017-01clarifies the definition of a business for determining whether transactions should be accounted for as acquisitions (or disposals) of assets or businesses. ASU2017-01 is effective for annual periods and interim periods within those annual periods beginning after December 15, 2017, and early adoption is permitted.The Company is in the process of evaluating the impact of the adoption of ASU 2017-01 on its consolidated financial statements. There are no other recently issued accounting pronouncements that are expected to have a material effect on the Company’s financial position, results ofoperations or cash flows. Item 7A. Quantitative and Qualitative Disclosures About Market Risk. Market Risk: The principal market risks (i.e., the risk of loss arising from adverse changes in market rates and prices) to which the Company is exposed are interest rates oncash and certain items in inventory. Interest Rate Risk: The Company earns interest on cash balances. In light of the Company’s existing cash, results of operations and projected borrowing requirements, theCompany does not believe that a 10% change in interest rates would have a significant impact on its consolidated financial position. Item 8. Financial Statements and Supplemental Data. The Company’s report from its independent registered public accounting firm and consolidated financial statements listed in the accompanying index is filedas part of this Annual Report. See “Index to Consolidated Financial Statements” on page F-1. Item 9. Changes in and Disagreements With Accountants on Accounting and Financial Disclosure. Not applicable. Item 9A. Controls and Procedures. Evaluation of Disclosure Controls and Procedures We maintain disclosure controls and procedures (as defined in Rules 13a-15(e) and 15d-15(e) under the Exchange Act) that are designed to providereasonable assurance that information required to be disclosed in reports we file or submit under the Exchange Act is recorded, processed, summarized andreported within the time periods specified in the rules and forms of the SEC and that such information is accumulated and communicated to our management,including the Chief Executive Officer and Chief Financial Officer, as appropriate, to allow timely decisions regarding required disclosures. All internal control systems, no matter how well designed and tested, have inherent limitations, including, among other things, the possibility of human error,circumvention or disregard. Therefore, even those systems of internal control that have been determined to be effective can provide only reasonableassurance that the objectives of the control system are met and may not prevent or detect misstatements. Also, projections of any evaluation of effectivenessto future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliance with thepolicies or procedures may deteriorate. 25 We carried out an evaluation, under the supervision and with the participation of management, of the effectiveness of the design and operation of ourdisclosure controls and procedures as of June 30, 2017. Based on this evaluation, our CEO and CFO have concluded that our disclosure controls andprocedures were effective as of June 30, 2017. Management’s Report on Internal Control over Financial Reporting Our management is responsible for establishing and maintaining adequate internal control over financial reporting and for assessing the effectiveness ofinternal control over financial reporting, as defined in Rule 13a-15(f) under the Exchange Act. Internal control over financial reporting refers to a processdesigned by, or under the supervision of, our CEO and our CFO and effected by our Board, management and other personnel, to provide reasonable assuranceregarding the reliability of financial reporting and the preparation of financial statements for external purposes in accordance with generally acceptedaccounting 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 dispositions of our assets; ●provide reasonable assurance that transactions are recorded as necessary to permit preparation of financial statements in accordance with generallyaccepted accounting principles, and that our receipts and expenditures are being made only in accordance with authorizations of our managementand members of our Board; and ●provide reasonable assurance regarding prevention or timely detection of unauthorized acquisition, use, or disposition of our assets that could havea material effect on our financial statements. Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluation ofeffectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliancewith the policies or procedures may deteriorate. Management conducted an evaluation of the effectiveness of our internal control over financial reporting as of June 30, 2017, based on the criteriaestablished in the 2013 Internal Control—Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission. Basedupon this evaluation, management has concluded that our internal control over financial reporting was effective as of June 30, 2017. Our independent registered public accounting firm, Grant Thornton LLP, has issued an attestation report on the effectiveness of our internal control overfinancial reporting as of June 30, 2017. Grant Thornton LLP’s report appears in Item 8 of this 10-K. Remediation of Previous Material Weaknesses in Internal Control Over Financial Reporting Our annual report on Form 10-K for the fiscal year ended June 30, 2016 and subsequent quarterly reports on Form 10-Q for the fiscal quarters endedSeptember 30, 2016, December 31, 2016 and March 31, 2017 (collectively, the “Prior Reports”) disclosed and described in detail material weaknesses ininternal control with respect to “tone at the top” and income tax process and procedures. As a result, the foregoing Prior Reports contained conclusions byour CEO and Interim CFO that our disclosure controls and procedures and internal control over financial reporting were not effective, as of the respectivedates of such Prior Reports. As further described in the Prior Reports, we have implemented a series of remedial actions to address these control deficiencies.We have since successfully completed the testing of these remediated controls and our conclusions with respect to disclosure controls and procedures andinternal control at June 30, 2017 are provided above. 26 Changes in Internal Control over Financial Reporting Other than remediation of material weaknesses disclosed in Prior Reports, there were no changes in our internal control over financial reporting (as such termis defined in Rules 13a-15(f) and 15d-15(f) under the Exchange Act) during the fourth fiscal quarter ended June 30, 2017 that materially affected, or arereasonably likely to materially affect, our internal control over financial reporting. Item 9B. Other Information. None. 27 PART III Item 10. Directors, Executive Officers and Corporate Governance. The Company currently has five Directors (the “Board”). Their term expires at the next Annual Meeting of Shareholders. The following table containsinformation regarding all Directors and executive officers of the Company as of June 30, 2017: Director Name Age Principal Occupation Since John W. Gildea 73 Director 2004 Dr. Charles Miner III 65 Director 2005 Stavros G. Vizirgianakis 46 President, Chief Executive Officer and Director 2013 Patrick A. McBrayer 65 Director 2014 Thomas M. Patton 53 Director 2015 Joseph P. Dwyer 61 Chief Financial Officer — Richard A. Zaremba 61 Senior Vice President, Secretary and Treasurer — Robert S. Ludecker 49 Senior Vice President, Global Sales and Marketing — Dan Voic 55 Vice President of Research and Development and Engineering — Joseph J. Brennan 54 Vice President of Operations — John J. Salerno 62 Vice President of Quality and Regulatory Affairs — Christopher H. Wright 43 Vice President of Domestic Sales — Principal Occupations and Business Experience of Directors and Executive Officers The following is a brief account of the business experience of the Company’s Directors and executive officers: Directors John W. Gildea, now retired, was the founding principal of Gildea Management Co., a management company of special situations with middle marketcompanies in the United States and Central Europe. From 2000 to 2003, Gildea Management formed a joint venture with J.O. Hambro Capital ManagementCo. to manage accounts targeting high yield debt and small capitalization equities. From 1996 to 2000, Gildea Management formed and founded LatonaEurope, a joint venture between Latona U.S., Lazard Co. and Gildea Management to restructure several Czech Republic companies. Before forming GildeaManagement in 1990, Mr. Gildea managed the Corporate Services Group at Donaldson, Lufkin and Jenrette, an investment banking firm. Mr. Gildea is agraduate of the University of Pittsburgh. Mr. Gildea has extensive experience as an international investment banker and sits on the board of severalcompanies. The Board believes this experience in addition to his experience as a Director of Misonix and knowledge of the Company qualifies him to serveas a Director. 28 Dr. Charles Miner III currently practices internal medicine in Darien, Connecticut. Dr. Miner is on staff at Stamford and Norwalk Hospitals and since 1982has held a teaching position at Columbia Presbyterian Hospital. Dr. Miner received his M.D. from the University of Cincinnati College of Medicine in 1979and received a Bachelor of Science from Lehigh University in 1974. Dr. Miner is an experienced physician and teacher in the medical field. He serves on theboard of The Stamford Hospital Foundation Board. The Board believes his experience as a medical doctor and his corporate experience qualifies him to serveas a Director. Stavros G. Vizirgianakis became the Company’s Interim Chief Executive Officer in September 2016 and its full-time President and Chief Executive Officerin December 2016. Mr. Vizirgianakis has a distinguished career in the medical devices field having worked for United States Surgical Corporation as directorof sales for sub-Saharan Africa and later Tyco Healthcare in the capacity of General Manager South Africa. In 2006, Mr. Vizirgianakis co-founded SurgicalInnovations, which has become one of the largest privately owned medical device distributors in the African region, and now part of the Johannesburg StockExchange listed entity Ascendis Health. In that capacity, Mr. Vizirgianakis acted as a distributor of the Company’s products. Mr. Vizirgianakis wasManaging Director of Ascendis Medical from January 2014 through July 2016. Mr. Vizirgianakis also served on the board of Tenaxis Medical and is astrategic investor and advisor to numerous medical device startups and established companies in this field. Mr. Vizirgianakis has a degree in commerce fromthe University of South Africa. The Board believes Mr. Vizirgianakis’ industry knowledge, sales and marketing experience and his vast international businessrelationships qualify him to serve as a Director. Patrick A. McBrayer has served since January 2016 as President and Chief Executive Officer of ACell Corporation, a surgery and wound care company. Mr.McBrayer previously served as President and Chief Executive Officer and as a director of privately-held AxioMed Spine Corporation from February 2006 toJanuary 2015. AxioMed is a medical device company focused on restoring the natural function of the spine. Prior to joining AxioMed, he held positions withXylos Corporation (medical biomaterials); Exogen, Inc. (treatment of musculoskeletal injury and disease); Osteotech, Inc. (tissue technology); and Johnsonand Johnson Products, Inc. (healthcare products). Mr. McBrayer holds a B. S. in General Engineering from the United States Military Academy. The Boardbelieves Mr. McBrayer’s industry knowledge and experience as a CEO qualifies him to serve as a Director. Thomas M. Patton has served as President and Chief Executive Officer of CAS Medical Systems, Inc. and as a member of its Board of Directors since August2010. He previously served as the CEO of Wright Medical Group, an orthopedic device company, located in Memphis, Tennessee, and as President ofNovametrix Medical Systems, a patient-monitoring company, located in Wallingford, Connecticut. From 2003 to 2010, Mr. Patton acted as an advisor to thehealthcare-focused private equity group of Ferrer Freeman & Company and, in that capacity, served as the interim CEO of Informed MedicalCommunications on a part-time basis in 2006 and 2007. Mr. Patton is a co-founder and CEO of QDx, Inc., a start-up company that developed a platform forhematology diagnostics beginning in 2003. Mr. Patton attended The College of the Holy Cross, where he majored in Economics and Accounting. Aftergraduating magna cum laude from Georgetown University Law Center, Mr. Patton worked at the law firm of Williams & Connolly in Washington, D.C.Thereafter, he joined Wright Medical Group as its General Counsel where he served in various executive roles until being appointed CEO. The Boardbelieves Mr. Patton’s industry knowledge and experience qualify him to serve as a director. Executive Officers who are not Directors Joseph P. Dwyer has served as the Company’s Chief Financial Officer since August 2017 and previously served as Interim Chief Financial Officer fromSeptember 2016. From June 2015 to the present, Mr. Dwyer has provided financial consulting and advisory services to various companies, through the firmsDwyer Holdings and TechCXO. Prior thereto, from November 2012 until June 2015, he was Chief Financial Officer of Virtual Piggy, Inc., a publicly-tradedtechnology company. Prior to joining Virtual Piggy, Mr. Dwyer served as chief financial officer of OpenLink Financial, Inc., a privately held company, whichprovides software solutions for trading and risk management in the energy, commodity, and capital markets. During 2011 and 2012, Mr. Dwyer was a memberof the board of directors and chairman of the audit committee and served as interim chief administrative officer of Energy Solutions International, Inc., aprivately-held company providing pipeline management software to energy companies and pipeline operators. From 2010 through 2011, Mr. Dwyer servedas chief administrative officer of Capstone Advisory Group, LLC, a privately- held financial advisory firm providing corporate restructuring, litigationsupport, forensic accounting, expert testimony and valuation services. Mr. Dwyer served as a consultant to Verint Systems, Inc., a software company listed onthe NASDAQ Global Market, from 2009 through 2010, assisting with SEC reporting and compliance. From 2005 through 2009, Mr. Dwyer served as chieffinancial officer and executive vice president of AXS-One Inc., a publicly traded software company. During 2004, Mr. Dwyer served as chief financial officerof Synergen, Inc., a privately held software company providing energy technology to utilities. Prior to 2004, Mr. Dwyer also served as chief financial officerand executive vice president of Caminus Corporation, an enterprise application software company that was formerly listed on the NASDAQ National Market,chief financial officer of ACTV, Inc., a digital media company that was formerly listed on the NASDAQ National Market, and chief financial officer ofWinstar Global Products, Inc., a manufacturer and distributor of hair care, bath and beauty products until its acquisition by Winstar Communications, Inc. in1995 when Mr. Dwyer went on to serve as senior vice president, finance of Winstar Communications. Mr. Dwyer received his BBA in Accounting from theUniversity of Notre Dame in 1978 and is licensed as a Certified Public Accountant in the State of New York. 29 Richard A. Zaremba became Senior Vice President and Chief Financial Officer in 2004. He became Vice President and Chief Financial Officer in February1999 and in September 2016, he became Senior Vice President, Finance. From March 1995 to February 1999, he was the Vice President and Chief FinancialOfficer of Converse Information Systems, Inc., a manufacturer of digital voice recording systems. Previously, Mr. Zaremba was Vice President and ChiefFinancial Officer of Miltope Group, Inc., a manufacturer of electronic equipment. Mr. Zaremba is a licensed certified public accountant in the State of NewYork and holds BBA and MBA degrees in Accounting from Hofstra University. Robert S. Ludecker became Senior Vice President of Global Sales and Marketing in May 2015. Prior to joining the Company as Global Vice President ofSales and Marketing in May 2013, Mr. Ludecker served from February 2011 to May 2013 as Vice President of Global Sales and Marketing for BioMimeticTherapeutics, a NASDAQ-listed biotechnology company, specializing in the development and commercialization of products which promote the healing ofmusculoskeletal injury and diseases, including orthopedic, spine, and sports medicine applications. Prior to BioMimetic, Mr. Ludecker served from February2008 to February 2011 in a variety of senior sales and marketing leadership positions with Small Bone Innovations, a private New York City-basedorthopedic company specializing in small bones, and Smith and Nephew, a leading U.K.-based global provider of orthopedic reconstruction implants and abroad portfolio of medical instruments and supplies. Mr. Ludecker holds a B. A. degree from Kenyon College. Dan Voic became Vice President of Research and Development and Engineering in January 2002. Prior thereto, he served as Engineering Manager andDirector of Engineering with the Company. Mr. Voic has in excess of 15 years’ experience in both medical and laboratory and scientific productsdevelopment. Mr. Voic holds an M.S. degree in mechanical engineering from Polytechnic University “Traian Vuia” of Timisoara, Romania and an MS degreein applied mechanics from Polytechnic University of New York. Joseph J. Brennan became Vice President of Operations in November 2014. Prior to joining the Company, Mr. Brennan served from October 2008 to August2014 as Director of Operations for Air Techniques, Inc., a global medical device company. Mr. Brennan holds a B. T. degree from the State University of NewYork at Farmingdale. John J. Salerno became Vice President of Quality and Regulatory Affairs in March 2015. Prior to joining the Company, Mr. Salerno served from December2012 to March 2015 as Senior Director of Quality Assurance for US Nonwovens Corp., a privately-held over the counter drug products, cosmetics, personalcare and EPA surface disinfectant company. From May 2010 to December 2012, Mr. Salerno was a consultant for US Nonwovens. From 2006 to 2010, Mr.Salerno held the position of Vice President of Quality Assurance and Regulatory Affairs for International Technidyne Corporation. Prior to 2006, Mr. Salernoheld the position of Vice President of Regulator Compliance and Reliability Engineering for Pall Life Sciences. Mr. Salerno holds a Master’s degree inMicrobiology from Long Island University and a Bachelor’s degree in biology from Fordham University. Christopher H. Wright became Vice President of Domestic Sales in July 2015. Prior to that, he was National Sales Director of Surgical Sales for the Companysince 2013. Prior to joining the Company, Mr. Wright served from 2011 to 2013 in the position of Senior Business Director with WrightMedical/BioMimetics, LLC. From 2007 – 2011 Mr. Wright held the position for Regional Manager with Small Bone Innovations. From 2005 – 2007 he heldthe position of Territory business manager with Baxter Healthcare. Prior to 2005, Mr. Wright was an independent sales representative. Mr. Wright holds aBachelor of Arts degree in Business Administration from Xavier University of New Orleans in Louisiana. 30 Executive officers are elected annually by, and serve at the discretion of, the Board. Section 16 (a) Beneficial Ownership Reporting Compliance Section 16(a) of the Exchange Act requires the Company’s executive officers, directors and persons who own more than 10% of a registered class of theCompany’s equity securities (“Reporting Persons”) to file reports of ownership and changes in ownership on Forms 3, 4, and 5 with the SEC. These ReportingPersons are required by SEC regulation to furnish the Company with copies of all Forms 3, 4 and 5 they file with the SEC. Based solely on the Company’sreview of the copies of the forms it has received, the Company believes that all Reporting Persons, complied on a timely basis with all filing requirementsapplicable to them with respect to transactions during fiscal year 2017, with the exception of one transaction by Robert Ludecker during fiscal 2015 whichwas omitted from the original Form 4 and was filed late, via amendment, in fiscal 2017. Code of Ethics The Company has adopted a code of ethics that applies to all of its directors, officers (including its Chief Executive Officer, Chief Financial Officer,Controller and any person performing similar functions) and employees. The Company has made the Code of Ethics available on its website atwww.MISONIX.com. Director Nomination Process The process followed by the Nominating and Governance Committee to identify and evaluate director candidates includes requests to the members of ourboard of directors and others for recommendations, meetings from time to time to evaluate biographical information and background material relating topotential candidates and interviews of selected candidates by members of the Nominating and Governance Committee and our board of directors. While we do not have a formal diversity policy for board membership, we look for potential candidates that help ensure that the board of directors has thebenefit of a wide range of attributes, including cultural, gender, ethnic and age diversity and experience in industries beyond healthcare. We also look forfinancial oversight experience, financial community experience and a good reputation within the financial community; business management experienceand the potential to succeed top management in the event board intervention is necessary on an unexpected basis; business contacts, business knowledgeand influence that may be useful to our businesses; and knowledge about our industry and technologies. Our board of directors does not currently prescribe any minimum qualifications for director candidates; however, the Nominating and Governance Committeewill take into account a potential candidate’s experience, areas of expertise and other factors relevant to the overall composition of our board of directors. Shareholders may recommend individuals to the Nominating and Governance Committee for consideration as potential director candidates by submitting thenames of the candidate(s), together with appropriate biographical information and background materials and a statement as to whether the shareholder orgroup of shareholders making the recommendation has beneficially owned more than 5% of our common stock for at least a year as of the date suchrecommendation is made, to the Nominating and Governance Committee, Attn: Corporate Secretary, Misonix, Inc., 1938 New Highway, Farmingdale, NewYork 11735. Assuming that appropriate biographical and background material has been provided on a timely basis, the Nominating and GovernanceCommittee will evaluate shareholder-recommended candidates by following substantially the same process, and applying substantially the same criteria, as itfollows for candidates submitted by others. 31 Audit Committee The Company has a separately-designated standing Audit Committee. The members of the Audit Committee are Messrs. Patton, Gildea and McBrayer. TheBoard of Directors has determined that each member of the Audit Committee is “independent” not only under the Corporate Governance Requirementsapplicable to Nasdaq-listed companies but also within the definition contained in a final rule of the SEC. Furthermore, the Board of Directors has determinedthat Mr. Gildea and Mr. Patton are “audit committee financial experts” within the definition contained in a final rule adopted by the SEC. Item 11. Executive Compensation. Compensation Discussion and Analysis Overview of Compensation Program and Philosophy Our compensation program is intended to: ●Attract, motivate, retain and reward employees of outstanding ability; ●Link changes in employee compensation to individual and corporate performance; ●Align employees’ interests with those of the Company’s shareholders. The ultimate objective of our compensation program is to increase shareholder value. We seek to achieve these objectives with a total compensationapproach which takes into account a competitive base salary, bonus pay based on the annual performance of the Company and individual goals and stockoption and restricted stock awards. The Board’s Compensation Committee, which is comprised solely of independent directors and is responsible for making decisions regarding the amount andform of compensation paid to the Company’s executive officers, has carefully considered the results of prior say-on-pay shareholder votes. Based upon thevote results at the most recent annual shareholders meeting, shareholders appear to be supportive of the Compensation Committee’s approach to theexecutive compensation program. Base Salaries Base salaries paid to executives are intended to attract and retain highly talented individuals. In setting base salaries, individual experience, individualperformance, the Company’s performance and job responsibilities during the year are considered. Executive salaries are reconciled by Human Resources andevaluated against local companies of similar size and nature. During the fiscal year ended June 30, 2017, Messrs. Ludecker, Voic and Zaremba each receivedbase salary increases of 3% based on performance. Annual Bonus Plan Compensation The Compensation Committee of the Board approves annual performance-based compensation. The purpose of the annual bonus-based compensation is tomotivate executive officers and key employees. Target bonuses, based upon recommendations from the Chief Executive Officer, are evaluated and approvedby the Compensation Committee for all management employees other than the Chief Executive Officer. The bonus recommendations are derived fromindividual and Company performance but not based on a specific formula and are discretionary. The Chief Executive Officer’s bonus compensation isderived from the recommendation of the Compensation Committee based upon the Chief Executive Officer’s performance and Company performance but isnot based on a specific formula and is discretionary. Bonuses earned in fiscal 2017 based on performance were as follows: $0 to Mr. Vizirgianakis, $0 to Mr.Dwyer, $0 to Mr. McManus, $0 to Mr. Zaremba, $82,500 to Mr. Ludecker , $22,000 to Mr. Voic, and $0 to Mr. Wright. Equity Incentive Awards Company executives are eligible to receive restricted stock and stock options (which give them the right to purchase shares of common stock at a specifiedprice in the future). These grants will vest based upon the passage of time, the achievement of performance metrics, or both. We believe that the use ofrestricted stock and stock options as the basis for long-term incentive compensation meets our defined compensation strategy and business needs byachieving increased value for shareholders and retaining key employees. 32 Stock option awards are intended to attract and retain highly talented executives, to provide an opportunity for significant compensation when overallCompany performance is reflected in the stock price and to help align executives’ and shareholders’ interests. Stock options are typically granted at the timeof hire to key new employees and annually to a broad group of existing key employees, including executive officers. We have adopted a number of equitycompensation plans governing the grant of such stock options. All of our equity compensation plans have been approved by our shareholders. Annual option grants to executive officers are made at the discretion of the Board or the Compensation Committee and may be in the form of incentive stockoptions (“ISOs”) up to the fullest extent permitted under tax laws, with the balance granted in the form of nonqualified stock options. The option grants aresubject to the terms of the relevant plan. ISOs have potential income tax advantage for executives if the executive disposes of the acquired shares aftersatisfying certain holding periods. Tax laws provide that at the date of grant, the aggregate fair market value of ISOs that become exercisable for anyemployee in any year may not exceed $100,000. Our current standard option vesting schedule for all employees is 25% on the first anniversary of the date of grant, 25% on the second anniversary of the dateof grant, 25% on the third anniversary of the date of grant and 25% on the fourth anniversary of the date of grant. We have on occasion issued options thathave two year vesting to employees. The number of stock options granted in fiscal 2017 to the named executive officers, and their estimated fair value, were as follows: Named Executive Officer Grant Date Number ofOptionsGranted EstimatedFair Value ofAwards atGrant Date Richard A. Zaremba 12/6/2016 30,000 $153,561 Robert S. Ludecker 11/3/2016 31,000 $110,689 Robert S. Ludecker 12/6/2016 30,000 $153,561 Dan Voic 12/6/2016 15,000 $76,781 Christopher H. Wright 11/3/2016 15,000 $53,559 Christopher H. Wright 12/6/2016 35,000 $179,155 The stock options awarded on November 3, 2016 had an exercise price of $6.76 (which was equal to the average of the opening and closing market price pershare of our stock on the date of grant). The stock options awarded on December 6, 2016 had an exercise price of $9.525 (which was equal to the average ofthe opening and closing market price per share of our stock on the date of grant). All stock options in the above table provide for vesting at 25% per year onthe first four year anniversary dates of the grant date, with a stated expiration date of ten years after grant. In conjunction with the execution of his employment agreement, on December 15, 2016 Mr. Vizirgianakis received grants of an aggregate of 400,000 sharesof restricted stock pursuant to the Company’s 2014 Employee Equity Incentive Plan (the “Plan”) as follows: (i) a grant of 134,000 shares vesting in five equalinstallments on September 1, 2017, 2018, 2019, 2020 and 2021; (ii) a performance grant of 133,000 shares which vests if both of the following conditions aresatisfied simultaneously: (A) at any time prior to the third anniversary of the grant date, the most recent publicly reported trailing four (4) fiscal quarterrevenue of the Company (exclusive of the impact of any acquisitions after the grant date) is at least $35,000,000 and (B) the closing price of the Company’sCommon Stock is at least $10.50 per share (subject to adjustment for stock splits, stock dividends and the like) for ten (10) consecutive trading days; and (iii)a performance grant of 133,000 shares which vests if both of the following conditions are satisfied simultaneously: (A) at any time prior to the fifthanniversary of the grant date, the most recent publicly reported trailing four (4) fiscal quarter revenue of the Company (exclusive of the impact of anyacquisitions after the grant date) is at least $48,000,000 and (B) the closing price of the Company’s Common Stock is at least $13.00 per share (subject toadjustment for stock splits, stock dividends and the like) for ten (10) consecutive trading days. The aforementioned performance grants will vest on a changeof control in accordance with the Plan only if the applicable share price threshold is met in such transaction. 33 Other Annual Compensation and Benefits Although direct compensation, in the form of salary, non-equity incentive awards and long-term equity incentive awards provide most of the compensationto each Executive Officer, we also provide for the following items of additional compensation: ●Retirement savings are provided by a 401(k) plan, in the same manner to all U.S. employees. This plan includes an employer matching contributionof 10% which is intended to encourage employees (including the chief executive officer) to save for retirement. ●Health, life and disability benefits are offered to our executive officers in the same manner to all of our U.S. employees. We provided additional lifeinsurance, long term care policies and certain transportation expenses for our chief executive officer and each of our executive officers. Transportation expenses are provided to executive officers, primarily in the form of an automobile allowance. Our former chief executive officer had the useof a Company provided automobile with driver. Compensation Committee Report Our Compensation Committee has furnished the following report. The information contained in the “Compensation Committee Report” is not deemed to be“soliciting material” or to be “filed” with the SEC, nor is such information to be incorporated by reference into any future filing under the Securities Act of1933, as amended (the “Securities Act”), or the Exchange Act, as amended, except to the extent that we specifically incorporate it by reference in to suchfilings. Our Compensation Committee has reviewed and discussed the “Compensation Discussion and Analysis” required by Item 402(b) of Regulation S-K of theSecurities Act with management. Based on such review and discussion, our Compensation Committee recommended to our Board of Directors that the“Compensation Discussion and Analysis” be included in our Annual Report on Form 10-K for the fiscal year ended June 30, 2017 for filing with the SEC. Compensation Committee Patrick A. McBrayer Dr. Charles Miner III Thomas M. Patton Compensation Committee Interlocks and Insider Participation During fiscal 2017, Messrs. Gildea, McBrayer, Patton and Miner and our former director, T. Guy Minetti served as members of our Compensation Committee.No Member of our Compensation Committee is or was during fiscal year 2017 an employee or an officer of Misonix or its Subsidiaries. 34 Grants of Plan Based Awards The following table presents non-equity and equity awards granted to the named executive officers in fiscal year 2017. GRANTS OF PLAN-BASED AWARDS IN FISCAL 2017 Name Grant Date (1) All Other Stock Awards: Number of Shares of Stock All Other Option Awards: Number of Securities Underlying Options (2)Exercise orBase priceof Option Awards($/Share) (3)Grant Date Fair Valueof Stockand Option Awards($) Stavros G. Vizirgianakis 12/15/2016 133,334 $— $1,286,400 Stavros G. Vizirgianakis 12/15/2016 133,333 $— $1,180,801 Stavros G. Vizirgianakis 12/15/2016 133,333 $— $1,170,187 Richard A. Zaremba 12/6/2016 30,000 $9.525 $153,561 Robert S. Ludecker 11/3/2016 31,000 $6.760 $110,689 Robert S. Ludecker 12/6/2016 30,000 $9.525 $153,561 Dan Voic 12/6/2016 15,000 $9.525 $76,781 Christopher H. Wright 11/3/2016 15,000 $6.760 $53,559 Christopher H. Wright 12/6/2016 35,000 $9.525 $179,155 (1)Mr. Vizirgianakis received restricted stock awards pursuant to our 2014 Equity Incentive Plan. (2)Stock option awards were issued on November 3, 2016 pursuant to our 2009 Equity Incentive Plan except for Mr. Wright who was awarded from the2012 Employee Equity Incentive Plan. Stock option awards were issued on December 6, 2016 pursuant to our 2014 Equity Incentive Plan except for Mr.Ludecker who was awarded from the 2012 Employee Equity Plan. All stock options in the above table provide for vesting at 25% per year on the firstfour year anniversary dates of the grant date, with a stated expiration date of ten years after grant. (3)This amount represents the Black-Scholes computation as of that date of award, except for Mr. Vizirgianakis, whose awards were valued using a MonteCarlo computation as of the grant date of the award. 35 Stock Option Exercises The following table shows all stock option exercises during fiscal 2017 by the named executive officers. OPTION EXERCISES IN FISCAL 2017 Name of Executive Officer Exercise Date Number of Shares Acquired On Exercise (1)Value Realized On Exercise Michael A. McManus, Jr. 5/22/2017 369,025 $2,899,540 Michael A. McManus, Jr. 6/14/2017 98,475 $391,850 Richard A. Zaremba 6/5/2017 3,000 $21,240 (1)Amounts reflect the difference between the exercise price of the options and the market value of the shares acquired upon exercise. Market values arebased on the closing price per share of our Common Stock on the NASDAQ Global Market on the date of exercise. Employment and Severance Agreements Vizirgianakis Employment Agreement On December 15, 2016, the Company entered into an Employment Agreement (the “Vizirgianakis Agreement”) with Stavros G. Vizirgianakis pursuant towhich Mr. Vizirgianakis serves as the Company’s full time President and Chief Executive Officer. Mr. Vizirgianakis had been serving on an unpaid basis asinterim Chief Executive Officer of the Company since September 2, 2016. Mr. Vizirgianakis continues to serve as a member of the Company’s Board ofDirectors. Pursuant to the Vizirgianakis Agreement, Mr. Vizirgianakis’ initial term of employment runs through September 13, 2019, provided that the term shall beautomatically renewed and extended for consecutive one (1) year renewal terms, unless either party sends to the other party a notice of non-renewal at leastninety (90) days prior to the expiration of the initial term or any then-current renewal term. Mr. Vizirgianakis will receive an annual base salary of not lessthan three hundred sixty thousand dollars ($360,000) per annum, subject to review by the Board at least annually for increase but not for decrease. Mr.Vizirgianakis is also eligible to receive annual bonuses in the discretion of the Board. The Vizirgianakis Agreement also provides for a one-time $10,000moving allowance and reimbursement of counsel fees relating to visa matters and the negotiation of the Vizirgianakis Agreement. If the Company terminatesMr. Vizirgianakis’ employment without cause (as defined in the Vizirgianakis Agreement), the Company provides a notice of non-renewal, or Mr.Vizirgianakis terminates his employment for good reason (as defined in the Vizirgianakis Agreement), Mr. Vizirgianakis shall be entitled to receive (i) alump-sum cash payment from the Company in an amount equal to one and one-half (1.5) times the annual base salary as is in effect immediately prior to thedate of such termination, and (ii) continuation of all employee benefits and fringe benefits to which he was entitled under the Vizirgianakis Agreementimmediately prior to such termination of employment for a period of eighteen (18) months following the termination of employment. The VizirgianakisAgreement also contains non-competition and non-solicitation covenants from Mr. Vizirgianakis during the term of employment and for a period of 18months thereafter. In conjunction with the execution of the Vizirgianakis Agreement, Mr. Vizirgianakis received grants of an aggregate of 400,000 shares of restricted stockpursuant to the Company’s 2014 Employee Equity Incentive Plan (the “Plan”) as follows: (i) a grant of 134,000 shares vesting in five equal installments onSeptember 1, 2017, 2018, 2019, 2020 and 2021; (ii) a performance grant of 133,000 shares which vests if both of the following conditions are satisfiedsimultaneously: (A) at any time prior to the third anniversary of the grant date, the most recent publicly reported trailing four (4) fiscal quarter revenue of theCompany (exclusive of the impact of any acquisitions after the grant date) is at least $35,000,000 and (B) the closing price of the Company’s Common Stockis at least $10.50 per share (subject to adjustment for stock splits, stock dividends and the like) for ten (10) consecutive trading days; and (iii) a performancegrant of 133,000 shares which vests if both of the following conditions are satisfied simultaneously: (A) at any time prior to the fifth anniversary of the grantdate, the most recent publicly reported trailing four (4) fiscal quarter revenue of the Company (exclusive of the impact of any acquisitions after the grant date)is at least $48,000,000 and (B) the closing price of the Company’s Common Stock is at least $13.00 per share (subject to adjustment for stock splits, stockdividends and the like) for ten (10) consecutive trading days. The aforementioned performance grants will vest on a change of control in accordance with thePlan only if the applicable share price threshold is met in such transaction. 36 McManus Employment Agreement On May 22, 2015, the Employment Agreement, dated July 1, 2014, by and between Michael A. McManus, Jr. and the Company was mutually terminated andreplaced by a new Employment Agreement whereby Mr. McManus continued to serve as the Company’s President and Chief Executive Officer (the“McManus Agreement”). The McManus Agreement, effective as of May 22, 2015, had an initial term expiring June 30, 2017 and would renew for successiveone-year periods thereafter unless terminated by either party not less than ninety (90) days prior to the end of the then-current term. The McManus Agreementprovided for an annual base salary of (i) $299,000 through June 30, 2015 and (ii) $325,000 commencing July 1, 2015, and an annual bonus based on Mr.McManus’ achievement of annual goals and objectives as determined by the Compensation Committee of the Company’s Board of Directors. Mr. McManusalso received a one-time grant of options to purchase 100,000 shares of Common Stock at an exercise price of $11.88 per share (the “McManus Options”). Mr. McManus was entitled under the McManus Agreement to participate in any plans and programs made available to the executive employees of theCompany generally. The Company could terminate the McManus Agreement for cause (as defined in the McManus Agreement). Mr. McManus could terminate the McManusAgreement for good reason (as defined in the McManus Agreement). If Mr. McManus terminated the McManus Agreement for good reason, the Company wasrequired to (i) pay him an amount equal to two times his total compensation (annual base salary plus bonus) at the highest rate paid him at any time duringthe aggregate time he has been employed by the Company, payable in a lump sum within sixty days of termination of employment, and (ii) pay premiums formedical, dental, vision, hospitalization and long term care coverage under Company plans for a period of twenty-four (24) months. Mr. McManus was entitled to severance pay and benefits if he terminated his employment with the Company following a Change in Control (as defined inthe McManus Agreement), to provide him with an incentive to remain with the Company and consummate a strategic corporate sale or transaction thatmaximizes shareholder value. Severance pay and benefits were triggered upon (i) his Involuntary Termination without Cause (as defined in the McManusAgreement) for a reason other than death or Disability (as defined in the McManus Agreement) or (ii) as a result of a Constructive Termination (as defined inthe McManus Agreement) which in either case occurs: (x) during the period not to exceed twenty-four (24) months after the effective date of a Change inControl, or (y) before the effective date of a Change in Control, but after the first date on which the Board of Directors and/or senior management of theCompany has entered into formal negotiations with a potential acquirer that results in the consummation of a Change in Control. In the event that pay and benefits are so triggered, Mr. McManus (A) was entitled to receive severance pay in an amount equal to two (2) times the sum of (a)his annual base pay and (b) bonus at the highest rate paid him for any fiscal year during the aggregate period of his employment by the Company, payable incash in a lump sum; the payment of premiums for medical, dental, vision, hospitalization and long term care coverage under Company plans for a period oftwenty-four (24) months; (B) had the right, for a period of (i) ninety (90) days for stock options granted under any of the Company’s Employee Stock OptionPlans adopted prior to 2005 and (ii) two (2) years for stock options granted under the Company’s 2005 Employee Equity Incentive Plan, 2009 EmployeeEquity Incentive Plan, 2014 Employee Equity Incentive Plan and any plan adopted after the effective date of the McManus Agreement, following hisTermination Date (as defined in the McManus Agreement) to exercise the options to the extent such options were otherwise vested and exercisable as of theTermination Date under the terms of the applicable stock option McManus Agreement(s) and plan(s); and (C) would vest in all unvested stock option grantswith respect to options granted after July 1, 2012. 37 Mr. McManus also agreed in the McManus Agreement to an eighteen month post-termination covenant not-to-compete, as well as other customary covenantsconcerning non-solicitation and non-disclosure of confidential information of the Company. The Company and Mr. McManus had previously entered into two letter agreements (the “Letter Agreements”) providing for the exercise of vested options byMr. McManus (i) for a ninety (90) day period after his retirement with respect to stock options granted under certain of the Company’s stock option plans and(ii) for two (2) years after Mr. McManus terminated his employment with the Company in the event of a Change-in-Control (as defined in the applicablestock option plans) and he was eligible for the severance benefits provided for by the McManus Agreement. The Company and Mr. McManus entered into aletter agreement to confirm that the terms and conditions of the Letter Agreements continued to be in full force and effect and apply to the McManusAgreement. McManus Retirement Agreement On August 26, 2016, the Company and Mr. McManus entered into a Retirement Agreement and General Release (the “Retirement Agreement”). Pursuant tothe Retirement Agreement, on September 2, 2016 Mr. McManus resigned as a Director and the Chairman of the Board of Directors of the Company andretired as President and Chief Executive Officer of the Company. Pursuant to the Retirement Agreement, which supersedes the McManus Agreement andletter agreements dated May 22, 2015, July 1, 2012 and July 1, 2012, respectively, the Company agreed to (i) pay Mr. McManus’ salary through June 30,2017 at the current level; (ii) continue to pay premiums for Mr. McManus’ and his dependents’ coverage under the Company’s medical, dental, vision,hospitalization, long term care and life insurance coverage through June 30, 2017 at the current levels upon timely election by Mr. McManus under the lawinformally known as COBRA; and (iii) extend the exercisability of previously granted and currently vested options to purchase shares of the Company’sCommon Stock through June 30, 2017. In addition, Mr. McManus had continued use of the vehicle provided him pursuant to the McManus Agreementthrough December 31, 2016. The Retirement Agreement provides for customary releases by the Company and Mr. McManus as well as customary provisions concerning confidentiality,non-disparagement and cooperation. The Retirement Agreement also provided that through June 30, 2017, upon request of the Company’s (i) Board of Directors or (ii) President and ChiefExecutive Officer, Mr. McManus would consult with the Company for up to ten (10) hours per month without compensation therefor except forreimbursement of reasonable travel expenses. Mr. McManus shall continue to be entitled to indemnification to the extent permitted to him by the Company’s By-Laws and Certificate of Incorporation.The Company has also agreed to maintain directors’ and officers’ liability insurance for Mr. McManus’ benefit, if any, that shall be no less favorable to himthan such insurance made available to or for the benefit of former directors or officers of the Company. Dwyer Employment Agreement On August 21, 2017, the Company entered into an Employment Agreement (the “Dwyer Agreement”) with Joseph P. Dwyer pursuant to which Mr. Dwyerserves as the Company’s full time Chief Financial Officer. Mr. Dwyer had been serving as Interim Chief Financial Officer of the Company since September 13,2016. Pursuant to the Dwyer Agreement, Mr. Dwyer’s initial term of employment runs through August 21, 2019, provided that the term shall be automaticallyrenewed and extended for consecutive one (1) year renewal terms, unless either party sends to the other party a notice of non-renewal at least ninety (90) daysprior to the expiration of the initial term or any then-current renewal term. Mr. Dwyer will receive an annual base salary of not less than two hundred seventy-five thousand dollars ($275,000) per annum, subject to review by the Board at least annually for increase but not for decrease. Mr. Dwyer is also eligible toreceive annual bonuses in the discretion of the Board. If the Company terminates Mr. Dwyer’ employment without cause (as defined in the DwyerAgreement), the Company provides a notice of non-renewal, or Mr. Dwyer terminates his employment for good reason (as defined in the Dwyer Agreement),Mr. Dwyer shall be entitled to receive (i) a lump-sum cash payment from the Company in an amount equal to fifty percent of the annual base salary if theapplicable termination of employment takes place prior to the first anniversary of the effective date of the Dwyer Agreement or one hundred percent of theannual base salary if the applicable termination of employment takes place on or at any time after the first anniversary of the effective date of the DwyerAgreement and (ii) continuation of all employee benefits and fringe benefits to which he was entitled under the Dwyer Agreement immediately prior to suchtermination of employment for a period of six or twelve months (as the case may be based upon the same time criteria as the cash severance) following thetermination of employment. The Dwyer Agreement also contains non-competition and non-solicitation covenants from Mr. Dwyer during the term ofemployment and for a period of 12 months thereafter. In conjunction with the execution of the Dwyer Agreement, Mr. Dwyer received a grant of a ten-year stock option to purchase one hundred thousand(100,000) shares (the “Dwyer Stock Option Award”) of Company common stock, under the Misonix, Inc. 2017 Equity Incentive Plan or another equity planadopted by the Board and approved by the Company’s shareholders. The Dwyer Stock Option Award has an exercise price of $10.20 per share, which equalsthe fair market value as defined in the plan and vests and becomes exercisable in four equal annual installments from the date of grant. Dwyer Consulting Agreement On September 13, 2016, the Company appointed Joseph Dwyer as the Company’s interim Chief Financial Officer, reporting to the Company’s ChiefExecutive Officer and Audit Committee. The Company entered into a Consulting Agreement, dated September 13, 2016, with Dwyer Holdings LLC (“DwyerCo.”) to provide Mr. Dwyer’s services to the Company (the “Dwyer Consulting Agreement”). The Dwyer Consulting Agreement was in effect for a one (1)year period, cancellable by either party upon five (5) days’ notice any time after the initial two (2) months of the term. Dwyer Co. was paid $30,000 per monthfor Mr. Dwyer’s services. On October 25, 2016, the Company entered into Amendment No. 1 to Consulting Agreement (the “Amendment”) with DwyerHoldings LLC. The Amendment amends the Dwyer Consulting Agreement solely to: (i) require that the Company provide Mr. Dwyer with coverage under itsdirectors’ and officers’ liability policy that is no less favorable than the coverage then provided to any other present or former executive, officer or director ofthe Company during the term of the Dwyer Consulting Agreement and for a period of at least five years thereafter and (ii) provide that should Mr. Dwyer berequired or requested by the Company to provide documentary evidence or testimony in connection with any claim or legal matter arising from or connectedwith the services provided under the Dwyer Consulting Agreement, the Company shall pay all reasonable expenses (including fees of legal counsel) incomplying therewith and, following the term of the Dwyer Consulting Agreement, $400 per hour for sworn testimony or preparation therefor payable inadvance. The Dwyer Consulting Agreement was superseded by the Dwyer Agreement described above. 38 Executive Severance Agreements On September 15, 2016, the Company and Richard A. Zaremba, Senior Vice President – Finance, entered into a letter agreement (the “Zaremba Agreement”)which provides that in the event (i) Mr. Zaremba’s employment with the Company is terminated by the Company on or before September 15, 2018 for anyreason other than for Cause (as defined in the Zaremba Agreement), the Company will pay him a one-time additional compensation equal to twelve (12)months annual base salary and (ii) of a Change in Control of Misonix (as defined in the Zaremba Agreement) and his employment by the Company or theacquiring company ceases (x) involuntarily or (y) voluntarily in accordance with the terms of the Zaremba Agreement, Mr. Zaremba will be entitled to a one-time additional compensation equal to twelve (12) months annual base salary. The Zaremba Agreement contains standard provisions regarding (i) executionof a release and covenant not to sue; (ii) cooperation; (iii) confidentiality; (iv) non-competition; (v) non-solicitation; and (vi) non-disparagement. On September 15, 2016, the Company and Robert S. Ludecker, Senior Vice President, Global Sales and Marketing, entered into a letter agreement (the“Ludecker Agreement”) which provides that in the event (i) Mr. Ludecker’s employment with the Company is terminated by the Company on or beforeSeptember 15, 2018 for any reason other than for Cause (as defined in the Ludecker Agreement), the Company will pay him a one-time additionalcompensation equal to twelve (12) months annual base salary and (ii) of a Change in Control of Misonix (as defined in the Ludecker Agreement) and hisemployment by the Company or the acquiring company ceases (x) involuntarily or (y) voluntarily in accordance with the terms of the Ludecker Agreement,Mr. Ludecker will be entitled to a one-time additional compensation equal to twelve (12) months annual base salary. The Ludecker Agreement containsstandard provisions regarding (i) execution of a release and covenant not to sue; (ii) cooperation; (iii) confidentiality; (iv) non-competition; (v) non-solicitation; and (vi) non-disparagement. Summary of Potential Payments Upon Termination or Following a Change-In-Control Severance Agreement and Severance Payments Except as described above, we did not have severance agreements with any of our Executive Officers during fiscal 2017. As described above under “-Employment and Severance Agreements,” we subsequently entered into a Retirement Agreement and General Release with our former Chief ExecutiveOfficer Michael A. McManus, Jr., governing the terms of his retirement from the Company and entered into severance letter agreements with Mr. Zaremba andMr. Ludecker that provide for payment of twelve (12) months annual base salary upon certain employment termination events. Change-in-Control and Change-in-Control Payments In the event of a change-in-control, we are required to make certain change-in-control payments to Mr. Zaremba, Mr. Ludecker, and Mr. Voic under the termsof the change-in-control agreements. The agreements provide for twelve (12) months base salary upon change in control of the Company. 39 The following table shows the benefits which would be received by each of our named executive officers for severance and change-in-control events: Severance Payments Change-in-Control Payments Employee Employee Equity Salary Benefits Total Salary Benefits Awards Total Stavros G. Vizirgianakis $540,000 $32,040 $572,040 $— $— $3,820,000 $3,820,000 Joseph P. Dwyer $137,500 $10,000 $147,500 $— $— $— $— Richard A. Zaremba $243,347 $— $243,347 $243,347 $— $89,725 $333,072 Robert S. Ludecker $275,843 $— $275,843 $275,843 $— $136,290 $912,133 Dan Voic $— $— $— $188,264 $— $80,425 $268,689 Christopher H. Wright $— $— $— $— $54,213 $54,213 Tax deductibility of Executive Compensation Section 162 (m) of the Code limits to $1,000,000 per person the amount that we may deduct for compensation paid to any of our most highly compensatedofficers in any year. In fiscal 2017, there was no executive officer’s compensation that exceeded $1,000,000 except for Stavros Vizirgianakis, our ChiefExecutive Officer, based on the valuation of his equity compensation. Summary of Compensation The table and footnotes below describe the total compensation paid for fiscal years ended June 30, 2017, June 30, 2016, and June 30, 2015 to the “namedexecutive officers,” who are each of the persons who served as our principal executive officer and principal financial officer during fiscal 2017, and the threeother most highly compensated individuals who were serving as executive officers of the Company on June 30, 2017, the last day of the fiscal year. 40 SUMMARY COMPENSATION TABLE All Name Fiscal year Other and Principal Ended Stock Option Compen- Position June 30, Salary ($) Bonus ($) Awards ($) Awards ($) sation ($) Total ($) Stavros Vizirgianakis 2017 $180,000 $3,637,388 $124,020(1) $3,941,408 President and Chief Executive 2016 — — — — — — Officer 2015 — — — — — — Joseph P. Dwyer 2017 $285,000 — — — — $285,000 Chief Financial Officer 2016 — — — — — — 2015 — — — — — — Michael A. McManus, Jr. 2017 $54,167 — — — $348,263(3) $402,430 Former President and Chief 2016 $325,000 — — $259,715 $99,730 $684,445 Executive Officer (2) 2015 $290,008 $100,000 — $1,314,695 $96,291 $1,800,994 Richard A. Zaremba 2017 $239,804 $— — $153,561 $15,093(5) $408,458 Senior Vice President of Finance, 2016 $232,819 $45,000 — $110,379 $10,081 $398,279 Secretary and Treasurer (4) 2015 $226,038 $25,000 — $178,374 $10,731 $440,143 Robert S. Ludecker 2017 $271,817 $82,500 — $264,250 $31,300(6) $649,867 Senior Vice President-Medical 2016 $263,900 $65,000 — $110,379 $8,194 $447,473 Global Sales and Marketing 2015 $215,098 $45,000 — $748,751 $8,376 $1,017,225 Dan Voic 2017 $185,523 $22,000 — $76,781 $15,615(7) $299,919 Vice President of 2016 $180,119 $25,000 — $128,776 $11,885 $345,780 Research and Development 2015 $174,873 $20,000 — $208,103 $12,147 $415,123 and Engineering Christopher H. Wright 2017 $383,250 — — $232,714 $10,870(8) $626,834 Vice President - U. S. Sales 2016 $296,300 — — $55,190 $7,646 $359,136 2015 $248,000 — — $59,458 $8,246 $315,704 (1)Includes $65,020 of legal fees related to his employment contract with the Company and his visa application process, $10,000 for relocation costs,$3,900 for a car allowance and $10,000 for director fees prior to being appointed as Chief Executive Officer. Stock awards assume that allperformance conditions are met. Refer to footnote 6 of the Consolidated Financial Statements for a description of the valuation method and inputsrelating to the stock awards. (2)Mr. McManus retired from the Company effective September 2, 2016. (3)Includes $270,833 of severance payments, $58,617 of expenses for a Company-owned automobile and a driver, $26,229 of life insurance benefitsand long term care insurance coverage. (4)On September 13, 2016, Mr. Zaremba (i) ceased serving as the Company’s Senior Vice President and Chief Financial Officer and (ii) was appointedSenior Vice President, Finance of the Company. He remains the Company’s Secretary and Treasurer. (5)Includes a car allowance, life and long term care insurance coverage. (6)Includes a $10,220 for a car allowance, life and long term care insurance coverage and $13,076 for a home security system. (7)Includes a car allowance, toll reimbursements and life and long term care insurance coverage. (8)Includes a car allowance, life and long term care insurance coverage. Outstanding Equity Awards at Fiscal Year-End The following table sets forth information regarding outstanding equity awards held as of June 30, 2017 by our named executive officers. 41 OUTSTANDING EQUITY AWARDS AT 2017 FISCAL YEAR END Name Number of Securities Underlying Unexercised Options (#) Exercisable Number of Securities Underlying Unexercised Options (#) Unexercisable OptionExercisePrice ($) OptionExpirationDate (1)Number ofShares ofStock ThatHave NotNot Vested MarketValue ofShares ofStock ThatHave NotVested Stavros G. Vizirgianakis $— 134,000 (11) $ 1,279,700 133,000 (11) $ 1,270,150 133,000 (11) $1,270,150 Richard A. Zaremba 7,000 —(1) 2.96 9/13/2022 10,000 10,000(3) 4.68 9/10/2023 7,500 15,000(4) 7.67 9/9/2024 7,500 22,500(7) 9.38 8/18/2025 — 30,000(10) 9.25 12/6/2026 Robert S. Ludecker 7,500 2,500(3) 4.68 9/10/2023 17,500 17,500(4) 7.67 9/9/2024 40,000 40,000(8) 12.77 5/14/2025 7,500 22,500(7) 9.38 8/18/2025 — 31,000(9) 6.76 11/3/2026 — 30,000(10) 9.52 12/6/2026 Dan Voic 7,500 — 2.19 9/13/2021 17,500 —(1) 2.96 9/13/2022 17,500 8,750(3) 4.68 9/10/2023 17,500 17,500(4) 7.67 9/9/2024 8,750 26,250(7) 9.38 8/18/2025 15,000(10) 9.52 12/6/2026 Christopher H. Wright 5,000 5,000(4) 7.67 9/9/2024 3,750 11,250(7) 9.38 8/18/2025 — 15,000(9) 6.76 11/3/2026 — 35,000(10) 9.52 12/6/2026 (1)Options issued 09/13/12 and vest equally over 4 years. (2)Options issued 12/05/12 and vest equally over 4 years. (3)Options issued 09/10/13 and vest equally over 4 years. (4)Options issued 09/09/14 and vest equally over 4 years. (5)Options issued 05/22/15 and vest on June 30, 2017. (6)Options issued 08/19/2015 and vest equally over 4 years. (7)Options issued 08/18/2015 and vest equally over 4 years. (8)Options issued 05/14/2015 and vest equally on 11/14/2016, 5/14/2017, 5/14/2018 and 5/14/2019. (9)Options issued on 11/3/16 and vested equally over 4 years. 42 (10)Options issued on 12/6/16 and vested equally over 4 years. (11)134,000 shares vesting in five equal installments on September 1, 2017, 2018, 2019, 2020 and 2021; 133,000 shares vest if both of the followingconditions are satisfied simultaneously: (A) at any time prior to the third anniversary of the grant date, the most recent publicly reported trailing four(4) fiscal quarter revenue of the Company (exclusive of the impact of any acquisitions after the grant date) is at least $35,000,000 and (B) the closingprice of the Company’s Common Stock is at least $10.50 per share (subject to adjustment for stock splits, stock dividends and the like) for ten (10)consecutive trading days; and 133,000 shares vest if both of the following conditions are satisfied simultaneously: (A) at any time prior to the fifthanniversary of the grant date, the most recent publicly reported trailing four (4) fiscal quarter revenue of the Company (exclusive of the impact ofany acquisitions after the grant date) is at least $48,000,000 and (B) the closing price of the Company’s Common Stock is at least $13.00 per share(subject to adjustment for stock splits, stock dividends and the like) for ten (10) consecutive trading days. Equity Plans As of June 30, 2017, the Company had the following stock plans with options or other grants outstanding or available for issuance: Available Initial Expired / For Plan Shares Granted Exercised Forfeited Outstanding Issuance 2001 Employee Stock Option Plan 1,000,000 1,251,261 376,368 868,955 5,938 — 2005 Employee Equity Incentive Plan 500,000 547,125 484,250 48,925 13,950 — 2005 Non Employee Director StockOption Plan 200,000 195,000 97,500 7,500 90,000 — 2009 Employee Equity Incentive Plan 500,000 619,925 357,227 123,100 139,598 3,175 2009 Non Employee Director StockOption Plan 200,000 195,000 48,750 33,750 112,500 38,750 2012 Employee Equity Incentive Plan 500,000 664,000 111,250 188,250 364,500 24,250 2012 Non Employee Director StockOption Plan 200,000 180,000 — 41,250 138,750 61,250 2014 Employee Equity Incentive Plan 750,000 480,000 — 154,000 326,000 24,000 2017 Equity Incentive Plan 750,000 — — — — 750,000 Total 1,191,236 901,425 Director Compensation Directors are compensated through payment of a cash fee and annual stock option grants. Commencing on January 1, 2017 and effective on May 9, 2017,each non-employee director received an annual fee of $35,000 and the Chairman of the Audit Committee received $45,000. Commencing February 3, 2015,each non-employee director received an annual fee of $20,000 and the Chairman of the Audit Committee received $25,000. Each non-employee director wasalso reimbursed for reasonable expenses incurred while traveling to attend a meeting of the Board of Directors or while traveling in furtherance of thebusiness of the Company. In May 2017, the Chairman of the Audit Committee received a one time additional payment of $25,000 in recognition of hisservices during the prior year. The following table sets forth information for the fiscal year ended June 30, 2017 with respect to the compensation of our directors. 43 DIRECTOR COMPENSATION FOR THE 2017 FISCAL YEAR Name Fees Earnedor Paid in Cash ($) OptionAwards ($) Total ($) John W. Gildea $23,750 $23,750 Dr. Charles Miner III $23,750 $23,750 T. Guy Minetti $11,250 $11,250 Stavros G. Vizirgianakis $10,000 $10,000 Thomas M. Patton $53,700 $53,700 Patrick A. McBrayer $23,750 $23,750 Outstanding options at June 30, 2017 for Messrs. Gildea and Miner were 90,000 shares each, Mr. Vizirgianakis was 37,500 shares, Mr. McBrayer was 30,000shares, Mr. Patton was 15,000 shares and Mr. Minetti was 75,000. Item 12. Security Ownership of Certain Beneficial Owners and Management and Related Stockholder Matters. The following table sets forth as of June 30, 2017, certain information with regard to the ownership of the Company’s Common Stock by (i) each beneficialowner of 5% or more of the Company’s Common Stock; (ii) each director; (iii) each executive officer named in the “Summary Compensation Table” above;and (iv) all executive officers and directors of the Company as a group. Unless otherwise stated, the persons named in the table have sole voting andinvestment power with respect to all Common Stock shown as beneficially owned by them. Name and Address (1) Common StockBeneficiallyOwned PercentOfClass Stavros G. Vizirgianakis 1,648,578(2) 17.6 Michael A. McManus, Jr. 636,868 6.8 John W. Gildea 97,500(3) 1.0 Patrick A. McBrayer 11,350(4) * Charles Miner 85,000(5) * Thomas M. Patton 3,750(6) * Richard A. Zaremba 171,023(7) 1.8 Robert S. Ludecker 84,943(8) * Dan Voic 216,395(9) 2.3 Christopher H. Wright 14,500(10) * Joseph P. Dwyer 500 * All executive officers and Directors as a group (Twelve people) 2,338,039(11) 24.0 * Less than 1% (1)Except as otherwise noted, the business address of each of the named individuals in this table is c/o MISONIX, INC., 1938 New Highway, Farmingdale,New York 11735. Michael A. McManus has an address at 100 White Plains Road, Bronxville, New York 10708. (2)Includes 15,000 shares which Mr. Vizirgianakis has the right to acquire upon exercise of stock options which are exercisable within 60 days. 44 (3)Includes 67,500 shares which Mr. Gildea has the right to acquire upon exercise of stock options which are exercisable within 60 days. (4)Includes 11,250 shares which Mr. McBrayer has the right to acquire upon exercise of stock options which are exercisable within 60 days. (5)Includes 67,500 shares which Dr. Miner has the right to acquire upon exercise of stock options which are exercisable within 60 days. (6)Consists of shares which Mr. Patton has the right to acquire upon exercise of stock options which are exercisable within 60 days. (7)Includes 39,500 shares which Mr. Zaremba has the right to acquire upon exercise of stock options which are exercisable within 60 days. (8)Includes 80,000 shares which Mr. Ludecker has the right to acquire upon exercise of stock options which are exercisable within 60 days. (9)Includes 77,500 shares which Mr. Voic has the right to acquire upon exercise of stock options which are exercisable within 60 days. (10)Includes 12,500 shares which Mr. Wright has the right to acquire upon exercise of stock options which are exercisable within 60 days. (11)Includes 378,000 shares which such persons have the right to acquire upon exercise of stock options which are exercisable within 60 days. 45 Equity Compensation Plan Information: Number of securities remaining available for Number of Weighted future securities to -average issuance be exercise under equity issued upon price of compensation exercise of outstanding plans outstanding options, (excluding options, warrants securities warrants and reflected in Plan category and rights rights column (a)) (a) (b) (c) Equity compensationplans approved bysecurity holders I.2001 Plan 5,938 $1.82 — II. 2005 Plan 13,950 $2.84 — III. 2005 Directors Plan 90,000 $3.04 — IV. 2009 Plan 139,598 $4.60 3,175 V. 2009 Directors Plan 112,500 $5.56 38,750 VI. 2012 Plan 364,500 $7.70 24,250 VII. 2012 Directors Plan 138,750 $9.96 61,250 VIII. 2014 Plan 326,000 $10.26 24,000 IX. 2017 Plan $— 750,000 Equity compensationplans not approved bysecurity holders — — — Total 1,191,236 $7.66 901,425 Item 13. Certain Relationships and Related Transactions, and Director Independence. Director Compensation Please see Item 11 - “Executive Compensation - Director Compensation” for a discussion of options granted and other compensation to our non-employeedirectors. Executive Compensation Please see Item 11 - “Executive Compensation” for additional information on compensation of our present and former executive officers. Informationregarding (1) an Employment Agreement, and a Retirement Agreement and General Release with Michael A. McManus, Jr., our former President and ChiefExecutive Officer, (2) letter agreements with Richard A. Zaremba, our Senior Vice President – Finance, and Robert S. Ludecker, our Senior Vice President,Global Sales and Marketing (3) an Employment Agreement with Stavros G. Vizirgianakis, our current President and Chief Executive Officer and (4) anEmployment Agreement and a prior Consulting Agreement with Joseph Dwyer, our Chief Financial Officer. Director Independence The Company is required to have a Board of Directors a majority of whom are “independent” as defined by the Corporate Governance Rules applicable toNasdaq-listed companies and to disclose those Directors that the Board has determined to be independent. Based on such definition, the Board hasdetermined that all directors other than Stavros G. Vizirgianakis, who is an officer of the Company, are independent. See “Item 10. Directors, ExecutiveOfficers of the Registrant and Corporate Governance”. 46 Item 14. Principal Accountant Fees and Services. Audit Fees Grant Thornton LLP (“Grant Thornton”) billed the Company $509,482 and $960,351 in the aggregate for services rendered for the audit of the Company’s2017 and 2016 fiscal years, respectively, and the review of the Company’s interim financial statements included in the Company’s Quarterly Reports onForm 10-Q for the Company’s 2017 and 2016 fiscal years, respectively. Audit-Related Fees Grant Thornton billed the Company $15,600 and $15,600 for audit-related services as defined by the SEC for the fiscal years ended June 30, 2017 and 2016respectively. The audit-related services were for the audits of the Company’s pension plan. Tax Fees Grant Thornton billed the company $0 and $31,200 for tax related services for the fiscal years ended June 30, 2017 and 2016 respectively. Policy on Pre-approval of Independent Registered Public Accounting Firm Services The charter of the Audit Committee provides for the pre-approval of all audit services and all permitted non-audit services to be performed for Misonix by theindependent registered public accounting firm, subject to the requirements of applicable law. The procedures for pre-approving all audit and non-auditservices provided by the independent registered public accounting firm include the Audit Committee reviewing audit-related services, tax services and otherservices. The Audit Committee periodically monitors the services rendered by and actual fees paid to the independent registered public accounting firm toensure that such services are within the parameters approved by the Audit Committee. 47 PART IV Item 15. Exhibits and Financial Statement Schedules. (a)1.The response to this portion of Item 15 is submitted as a separate section of this Report. 2.Financial Statement Schedules Schedule II - Valuation and Qualifying Accounts. 3.Exhibits 3 (a)Restated Certificate of Incorporation of the Company. (1) 3 (b)By-laws of the Company. (2) 10.1Form of Indemnification Agreement. (3) 10.2Development and Option Agreement dated August 27, 1996 between the Company and United States Surgical Corporation. (4) 10.3License Agreement dated October 16, 1996 between the Company and United States Surgical Corporation. (4) 10.41996 Non-Employee Director Stock Option Plan. (5) 10.51996 Employee Incentive Stock Option Plan. (5) 10.61998 Employee Stock Option Plan. (6) 10.72001 Employee Stock Option Plan. (7) 10.82005 Employee Equity Incentive Plan. (8) 10.92005 Non-Employee Director Stock Option Plan. (8) 10.102009 Employee Equity Incentive Plan. (9) 10.112009 Non-Employee Director Stock Option Plan. (9) 10.12Asset Purchase Agreement, dated as of May 28, 2010, among MISONIX, INC., MISONIX HIFU TECHNOLOGIES LIMITED, MISONIXLIMITED and USHIFU, LLC. (10) 10.13Letter Agreement, dated November 14, 2011, by and between MISONIX, INC. and Richard A. Zaremba. (11) 10.14Letter Agreement, dated as of July 1, 2012, by and between MISONIX, INC. and Michael A. McManus, Jr. (12) 10.15Letter Agreement, dated as of July 1, 2012, by and between MISONIX, INC. and Michael A. McManus, Jr. (12) 48 10.16Letter Agreement, dated May 7, 2013 by and between MISONIX, INC. and Stavros G. Vizirgianakis. (13) 10.172012 Employee Equity Incentive Plan. (14) 10.182012 Non-Employee Director Stock Option Plan. (14) 10.192014 Employee Equity Incentive Plan. (15) 10.20Employment Agreement, dated May 22, 2015, by and between MISONIX, INC. and Michael A. McManus, Jr. (16) 10.21Letter Agreement, dated as of May 22, 2015, by and between MISONIX, INC. and Michael A. McManus, Jr. (16) 10.22Lease Modification Agreement, dated as of July 1, 2015, between Sanwood Realty and MISONIX, INC. (17) 10.23Retirement Agreement and General Release, dated August 26, 2016, between Michael A. McManus, Jr. and MISONIX, INC (18) 10.24Consulting Agreement, dated September 13, 2016, by and between MISONIX, INC. and Dwyer Holdings LLC (19) 10.25Letter Agreement, dated September 15, 2016, by and between MISONIX, INC. and Richard A. Zaremba (20) 10.26Letter Agreement, dated September 15, 2016, by and between MISONIX, INC. and Robert S. Ludecker (20) 10.27Stock Purchase Agreement dated October 25, 2016 between MISONIX, INC. and Stavros G. Vizirgianakis (21) 10.28Amendment No. 1 to Consulting Agreement between the Company and Joseph Dwyer dated October 25, 2016 (21) 10.29Employment Agreement dated December 15, 2016 between the Company and Stavros G. Vizirgianakis (22) 10.30Restricted Stock Award Agreement dated December 15, 2016 between the Company and Stavros G. Vizirgianakis (22) 10.31Restricted Stock Award Agreement dated December 15, 2016 between the Company and Stavros G. Vizirgianakis (22) 10.32Restricted Stock Award Agreement dated December 15, 2016 between the Company and Stavros G. Vizirgianakis (22) 10.332017 Equity Incentive Plan (23) 21Subsidiaries of the Company 23Consent of Grant Thornton LLP 49 31.1Rule 13a-14(a)/15d-14(a) Certification 31.2Rule 13a-14(a)/15d-14(a) Certification 32.1Section 1350 Certification 32.2Section 1350 Certification 101.INSXBRL Instance Document 101.SCHXBRL Taxonomy Extension Scheme Document 101.CALXBRL Taxonomy Extension Calculation Linkbase Document 101.DEFXBRL Taxonomy Extension Definition Linkbase Document 101.LABXBRL Taxonomy Extension Label Linkbase Document 101.PREXBRL Taxonomy Extension Presentation Linkbase Document (1)Incorporated by reference from the Company's Registration Statement on Form S-8 (Reg. No. 333-165088). (2)Incorporated by reference from the Company's Current Report on Form 8-K filed on October 3, 2014. (3)Incorporated by reference from the Company’s Annual Report on Form 10-K for the fiscal year ended June 30, 2011. (4)Incorporated by reference from the Company's Annual Report on Form 10-KSB for the fiscal year ended June 30, 1997. (5)Incorporated by reference from the Company's definitive proxy statement for the Annual Meeting of Shareholders held on February 19, 1997. (6)Incorporated by reference from the Company's Registration Statement on Form S-8 (Reg. No. 333-78795). (7)Incorporated by reference from the Company’s Registration Statement on Form S-8 (Reg. No. 333-63166). (8)Incorporated by reference from the Company's definitive proxy statement for the Annual Meeting of Shareholders held on December 14, 2005. (9)Incorporated by reference from the Company's definitive proxy statement for the Annual Meeting of Shareholders held on December 8, 2009. (10)Incorporated by reference from the Company's Current Report on Form 8-K filed on June 4, 2010. (11)Incorporated by reference from the Company’s Current Report on Form 8-K filed on November 15, 2011. (12)Incorporated by reference from the Company’s Current Report on Form 8-K filed on September 13, 2012. (13)Incorporated by reference from the Company’s Current Report on Form 8-K filed on May 10, 2013. 50 (14)Incorporated by reference from the Company’s definitive proxy statement for the Annual Meeting of Shareholders held on December 4, 2012. (15)Incorporated by reference from the Company’s definitive proxy statement for the Annual Meeting of Shareholders held on February 3, 2015. (16)Incorporated by reference by the Company’s Current Report on Form 8-K filed on May 26, 2015. (17)Incorporated by reference from the Company’s Current Report on Form 8-K filed on July 8, 2015. (18)Incorporated by reference from the Company’s Current Report on Form 8-K filed on August 26, 2016. (19)Incorporated by reference from the Company’s Current Report on Form 8-K filed on September 14, 2016. (20)Incorporated by reference from the Company’s Current Report on Form 8-K filed on September 16, 2016. (21)Incorporated by reference from the Company’s Current Report on Form 8-K filed on October 25, 2016. (22)Incorporated by reference from the Company’s Current Report on Form 8-K filed on December 19, 2016. (23)Incorporated by reference from the Company’s Registration Statement on Form S-8 filed on July 19, 2017. Item 16. Form 10-K Summary Not applicable. 51 SIGNATURES 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 itsbehalf by the undersigned, thereunto duly authorized. MISONIX, INC. By:/s/ Stavros G. Vizirgianakis Stavros G. Vizirgianakis Chief Executive Officer Date: August 24, 2017 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 registrantand in the capacities and on the dates indicated. Signature Title Date /s/ Stavros G. Vizirgianakis Chief Executive Officer and Director August 24, 2017Stavros G. Vizirgianakis (principal executive officer) /s/ Joseph P. Dwyer Chief Financial Officer August 24, 2017 Joseph P. Dwyer (principal financial and accounting officer) /s/ Patrick A. McBrayer Director August 24, 2017 Patrick A. McBrayer /s/ John W. Gildea Director August 24, 2017 John W. Gildea /s/ Charles Miner III Director August 24, 2017 Charles Miner III /s/ Thomas M. Patton Director August 24, 2017Thomas M. Patton 52 INDEX TO CONSOLIDATED FINANCIAL STATEMENTSMISONIX, INC. and SubsidiariesFor the years ended June 30, 2017, June 30, 2016 and June 30, 2015 PageReport of Independent Registered Public Accounting Firm F-2 Report of Independent Registered Public Accounting Firm F-3 Consolidated Balance Sheets - June 30, 2017 and 2016 F-4 Consolidated Statements of Operations - Years Ended June 30, 2017, 2016 and 2015 F-5 Consolidated Statements of Shareholders’ Equity - Years Ended June 30, 2017, 2016 and 2015 F-6 Consolidated Statements of Cash Flows - Years Ended June 30, 2017, 2016 and 2015 F-7 Notes to Consolidated Financial Statements F-8 The following consolidated financial statement schedule is included in Item 15(a)(2): Schedule II - Valuation and Qualifying Accounts F-26 All other schedules for which provision is made in the applicable accounting regulations of the SEC are not required under the related instructions or are notapplicable and therefore have been omitted. F-1 REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRMBoard of Directors and ShareholdersMISONIX, INC. We have audited the accompanying consolidated balance sheets of MISONIX, INC. and Subsidiaries (collectively, the “Company”) as of June 30, 2017 and2016, and the related consolidated statements of operations, shareholders’ equity and cash flows for each of the three years in the period ended June 30, 2017.Our audits of the basic consolidated financial statements included the financial statement schedule listed in the index appearing under Item 15(a)(2). Thesefinancial statements and financial statement schedule are the responsibility of the Company’s management. Our responsibility is to express an opinion onthese financial statements and financial statement schedule based on our audits. We conducted our audits in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those standards require thatwe plan and perform the audit to obtain reasonable assurance about whether the financial statements are free of material misstatement. An audit includesexamining, on a test basis, evidence supporting the amounts and disclosures in the financial statements. An audit also includes assessing the accountingprinciples used and significant estimates made by management, as well as evaluating the overall financial statement presentation. We believe that our auditsprovide a reasonable basis for our opinion. In our opinion, the consolidated financial statements referred to above present fairly, in all material respects, the financial position of MISONIX, INC. andSubsidiaries as of June 30, 2017 and 2016, and the results of their operations and their cash flows for each of the three years in the period ended June 30,2017 in conformity with accounting principles generally accepted in the United States of America. Also in our opinion, the related financial statementschedule, when considered in relation to the basic consolidated financial statements taken as a whole, present fairly, in all material respects, the informationset forth therein. We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), the Company’s internal controlover financial reporting as of June 30, 2017, based on criteria established in the 2013 Internal Control—Integrated Framework issued by the Committee ofSponsoring Organizations of the Treadway Commission (COSO), and our report dated August 24, 2017 expressed an unqualified opinion. /s/ GRANT THORNTON LLP Boston, MassachusettsAugust 24, 2017 F-2 REPORT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM Board of Directors and ShareholdersMISONIX, INC. We have audited the internal control over financial reporting of MISONIX, INC. and Subsidiaries (the “Company”) as of June 30, 2017, based on criteriaestablished in the 2013 Internal Control—Integrated Framework issued by the Committee of Sponsoring Organizations of the Treadway Commission(COSO). The Company’s management is responsible for maintaining effective internal control over financial reporting and for its assessment of theeffectiveness of internal control over financial reporting, included in the accompanying Management’s Report on Internal Control Over Financial Reporting(“Management’s Report”). Our responsibility is to express an opinion on the Company’s internal control over financial reporting based on our audit. We conducted our audit in accordance with the standards of the Public Company Accounting Oversight Board (United States). Those standards require thatwe plan and perform the audit to obtain reasonable assurance about whether effective internal control over financial reporting was maintained in all materialrespects. Our audit included obtaining an understanding of internal control over financial reporting, assessing the risk that a material weakness exists, testingand evaluating the design and operating effectiveness of internal control based on the assessed risk, and performing such other procedures as we considerednecessary in the circumstances. We believe that our audit provides a reasonable basis for our opinion. A company’s internal control over financial reporting is a process designed to provide reasonable assurance regarding the reliability of financial reportingand the preparation of financial statements for external purposes in accordance with generally accepted accounting principles. A company’s internal controlover financial reporting includes those policies and procedures that (1) pertain to the maintenance of records that, in reasonable detail, accurately and fairlyreflect the transactions and dispositions of the assets of the company; (2) provide reasonable assurance that transactions are recorded as necessary to permitpreparation of financial statements in accordance with generally accepted accounting principles, and that receipts and expenditures of the company are beingmade only in accordance with authorizations of management and directors of the company; and (3) provide reasonable assurance regarding prevention ortimely detection of unauthorized acquisition, use, or disposition of the company’s assets that could have a material effect on the financial statements. Because of its inherent limitations, internal control over financial reporting may not prevent or detect misstatements. Also, projections of any evaluation ofeffectiveness to future periods are subject to the risk that controls may become inadequate because of changes in conditions, or that the degree of compliancewith the policies or procedures may deteriorate. In our opinion, the Company maintained, in all material respects, effective internal control over financial reporting as of June 30, 2017, based on criteriaestablished in the 2013 Internal Control—Integrated Framework issued by COSO. We also have audited, in accordance with the standards of the Public Company Accounting Oversight Board (United States), the consolidated financialstatements of the Company as of and for the year ended June 30, 2017, and our report dated August 24, 2017 expressed an unqualified opinion on thoseconsolidated financial statements. /s/ GRANT THORNTON LLP Boston, MassachusettsAugust 24, 2017 F-3 MISONIX, INC. and SubsidiariesConsolidated Balance Sheets June 30,2017 June 30,2016 Assets Current assets: Cash and cash equivalents $11,557,071 $9,049,327 Accounts receivable, less allowance for doubtful accounts of $96,868 and $96,868, respectively 5,133,389 3,869,427 Inventories, net 4,992,434 5,822,935 Prepaid expenses and other current assets 918,899 530,564 Total current assets 22,601,793 19,272,253 Property, plant and equipment, net of accumulated amortization and depreciation of $7,794,580 and $6,976,282,respectively 3,730,203 2,492,815 Patents, net of accumulated amortization of $995,568 and $885,394, respectively 719,136 604,916 Goodwill 1,701,094 1,701,094 Intangible and other assets 282,876 266,603 Deferred income tax 4,334,547 3,394,690 Total assets $33,369,649 $27,732,371 Liabilities and shareholders’ equity Current liabilities: Accounts payable $1,861,228 $1,402,797 Accrued expenses and other current liabilities 3,346,138 1,887,337 Total current liabilities 5,207,366 3,290,134 Deferred lease liability 9,354 9,262 Deferred income 13,087 31,685 Total liabilities 5,229,807 3,331,081 Commitments and contingencies (Note 7) Shareholders’ equity: Common stock, $.01 par value-shares authorized 20,000,000; 9,357,166 and 7,948,234 shares issued and 9,357,166and 7,809,385 outstanding in each period, respectively 93,572 79,482 Additional paid-in capital 36,808,810 32,502,521 Accumulated deficit (8,762,540) (7,081,361)Treasury stock, at cost, 0 and 138,849 shares, respectively — (1,099,352)Total shareholders’ equity 28,139,842 24,401,290 Total liabilities and shareholders’ equity $33,369,649 $27,732,371 See Accompanying Notes to Consolidated Financial Statements. F-4 MISONIX, INC. and SubsidiariesConsolidated Statements of Operations For the years ended June 30, 2017 2016 2015 Net sales $27,269,963 $23,113,194 $22,204,578 Cost of goods sold 8,217,439 7,640,626 7,280,276 Gross profit 19,052,524 15,472,568 14,924,302 Operating expenses: Selling expenses 14,220,907 12,632,961 9,062,695 General and administrative expenses 9,595,206 6,829,516 5,983,623 Research and development expenses 1,837,497 1,839,479 1,592,923 Total operating expenses 25,653,610 21,301,956 16,639,241 Loss from operations (6,601,086) (5,829,388) (1,714,939) Other income (expense): Interest income 75 81 75 Royalty income and license fees 3,771,610 3,948,757 4,256,321 Other (36,211) (21,878) (22,033)Total other income 3,735,474 3,926,960 4,234,363 (Loss)/income from continuing operations before income taxes (2,865,612) (1,902,428) 2,519,424 Income tax (benefit)/expense (1,022,808) (573,351) (2,784,632) Net (loss)/income from continuing operations (1,842,804) (1,329,077) 5,304,056 Discontinued operations: Income from discontinued operations net of tax of $0, $0 and $1,127, respectively — — 17,115 Gain from sale of discontinued operations net of tax of $88,375, $93,069 and $0, respectively 161,625 156,931 250,000 Net income from discontinued operations 161,625 156,931 267,115 Net (loss)/income $(1,681,179) $(1,172,146) $5,571,171 Net (loss)/income per share from continuing operations - Basic $(0.22) $(0.17) $0.70 Net income per share from discontinued operations - Basic 0.02 0.02 0.04 Net (loss)/income per share - Basic $(0.20) $(0.15) $0.74 Net (loss)/income per share from continuing operations - Diluted $(0.22) $(0.17) $0.66 Net income per share from discontinued operations - Diluted 0.02 0.02 0.03 Net (loss)/income per share - Diluted $(0.20) $(0.15) $0.69 Weighted average shares - Basic 8,398,778 7,776,949 7,580,450 Weighted average shares - Diluted 8,398,778 7,776,949 8,094,119 See Accompanying Notes to Consolidated Financial Statements. F-5 MISONIX, INC. and SubsidiariesConsolidated Statements of Shareholders’ Equity Common Stock, $.01 Par Value Treasury Stock Additional Total Number Number paid-in Accumulated stockholders’ of shares Amount of shares Amount capital deficit equity Balance, June 30, 2014 7,412,096 $74,121 (77,560) $(410,993) $28,169,622 $(11,480,386) $16,352,364 Net income — — — — — 5,571,171 5,571,171 Proceeds from exercise of stock options 456,999 4,570 (47,422) (535,267) 1,254,257 — 723,560 Stock-based compensation — — — — 1,107,250 — 1,107,250 Balance, June 30, 2015 7,869,095 $78,691 (124,982) $(946,260) $30,531,129 $(5,909,215) $23,754,345 Net (loss) — — — — — (1,172,146) (1,172,146)Proceeds from exercise of stock options 79,139 791 (13,867) (153,092) 341,748 — 189,447 Stock-based compensation — — — — 1,629,644 — 1,629,644 Balance, June 30, 2016 7,948,234 $79,482 (138,849) $(1,099,352) $32,502,521 $(7,081,361) $24,401,290 Net (loss) — — — — — (1,681,179) (1,681,179)Sale of common stock 761,469 7,615 — — 3,992,385 4,000,000 Issuance of restricted stock 400,000 4,000 (4,000) — — Proceeds from exercise of stock options 247,463 2,475 138,849 1,099,352 (768,235) — 333,592 Stock-based compensation — — — — 1,086,139 — 1,086,139 Balance, June 30, 2017 9,357,166 $93,572 — $— $36,808,810 $(8,762,540) $28,139,842 See Accompanying Notes to Consolidated Financial Statements. F-6 MISONIX, INC. and SubsidiariesConsolidated Statements of Cash Flows For the years ended June 30, 2017 2016 2015 Operating activities Net (loss)/income from continuing operations $(1,842,804) $(1,329,077) $5,304,056 Adjustments to reconcile net (loss)/income to net cash provided by (used in) continuing operatingactivities: Depreciation and amortization and other non-cash items 1,066,844 1,651,972 1,439,972 Bad debt expense — (30,000) (10,000)Deferred income tax benefit (939,857) (502,262) (2,892,428)Stock-based compensation 1,086,139 1,629,644 1,107,250 Deferred income (18,598) (8,966) (46,052)Deferred lease liability 92 9,262 (16,614)Changes in operating assets and liabilities: Accounts receivable (1,263,962) 641,820 (712,095)Inventories (873,136) (2,823,304) (1,259,986)Prepaid expenses and other assets (404,608) (186,211) (129,828)Accounts payable, accrued expenses 1,917,232 630,882 (412,936)Net cash (used in)/provided by continuing operations (1,272,658) (316,240) 2,371,339 Investing activities Acquisition of property, plant and equipment (490,421) (471,829) (345,312)Payments for assets acquisition — — (328,136)Additional patents (224,394) (132,731) (104,755)Net cash used in investing activities from continuing operations (714,815) (604,560) (778,203) Financing activities Proceeds from sale of common stock 4,000,000 — — Proceeds from exercise of stock options 333,592 189,447 723,560 Net cash provided by financing activities from continuing operations 4,333,592 189,447 723,560 Cash flows from discontinued operations Net cash provided by operating activities — — 17,115 Net cash provided by investing activities 161,625 156,931 250,000 Net cash provided by discontinued operations 161,625 156,931 267,115 Net (decrease)/increase in cash and cash equivalents 2,507,744 (574,422) 2,583,811 Cash and cash equivalents at beginning of period 9,049,327 9,623,749 7,039,938 Cash and cash equivalents at end of period $11,557,071 $9,049,327 $9,623,749 Supplemental disclosure of cash flow information: Cash paid for: Income taxes $10,179 $140,931 $73,568 See Accompanying Notes to Consolidated Financial Statements. F-7 MISONIX, INC. and SubsidiariesNotes to Consolidated Financial StatementsFor the Years Ended June 30, 2017, 2016, and 2015 1. Basis of Presentation, Organization and Business and Summary of Significant Accounting Policies Basis of Presentation These consolidated financial statements of Misonix, Inc. (“Misonix” or the “Company”) include the accounts of Misonix and its 100% owned subsidiaries.All significant intercompany balances and transactions have been eliminated. Reclassifications Certain historical expenses on the Statement of Operations have been reclassified to be consistent with the current year presentation. Historically, theCompany had recorded stock compensation expense and bonus expense predominantly within general and administrative expenses. The Company hasreclassified amounts to allocate certain of these costs to cost of goods sold, selling expenses and research and development expenses, which is consistent withthe classification being used in 2017. This reclassification had no impact on the Company’s presentation of operating income (loss) and the gross profitimpact was not material. Organization and Business Misonix designs, manufactures, develops and markets therapeutic ultrasonic devices. These products are used for precise bone sculpting, removal of softtumors, and tissue debridement in the fields of orthopedic surgery, plastic surgery, neurosurgery, podiatry and vascular surgery. In the United States, theCompany sells its products through a network of commissioned agents assisted by Company personnel. Outside of the United States, the Company sells todistributors who then resell the product to hospitals. The Company operates as one business segment. High Intensity Focused Ultrasound Technology The Company sold its rights to the high intensity focused ultrasound technology to SonaCare Medical, LLC (“SonaCare”) in May 2010. The Company mayreceive up to approximately $5.8 million in payment for the sale. SonaCare will pay the Company 7% of the gross revenues received from its sales of the (i)prostate product in Europe and (ii) kidney and liver products worldwide, until the Company has received payments of $3 million, and thereafter 5% of thegross revenues, up to an aggregate payment of $5.8 million, all subject to a minimum annual royalty of $250,000. Cumulative payments through June 30,2017 were $1,504,788. Cash and Cash Equivalents The Company considers all highly liquid debt instruments purchased with a maturity of three months or less to be cash equivalents. All of the Company’scash is maintained in bank accounts and accordingly it does not have cash equivalents at June 30, 2017. The Company’s cash balance at June 30, 2017 was$11,557,071. The Company maintains cash balances at various financial institutions. At June 30, 2017, these financial institutions held cash that was approximately$11,325,285in excess of amounts insured by the Federal Deposit Insurance Corporation and other government agencies. F-8 Major Customers and Concentration of Credit Risk Included in sales from continuing operations are sales to Cicel of $46,722, $1,557,132 and $2,974,086, for the fiscal years ended June 30, 2017, 2016 and2015, respectively. There were no accounts receivable from Cicel at June 30, 2017 and 2016. The Company terminated its agreement with Cicel in the firstquarter of fiscal 2017. Total royalties from Medtronic Minimally Invasive Therapies (“MMIT”) related to their sales of the Company’s ultrasonic cutting and sculpting products,which use high frequency sound waves to coagulate and divide tissue for both open and laparoscopic surgery, were $3,764,000 , $3,903,000 and $4,162,000for the fiscal years ended June 30, 2017, 2016 and 2015, respectively. Accounts receivable from MMIT royalties were approximately $925,000 and $973,000at June 30, 2017 and 2016, respectively. The license agreement with MMIT expired in August 2017. At June 30, 2017 and 2016, the Company’s accounts receivable with customers outside the United States were approximately $860,000 and $768,000,respectively, none of which is over 90 days. Use of Estimates The preparation of financial statements in conformity with accounting principles generally accepted in the United States requires management to makeestimates and judgments that affect the reported amount of assets and liabilities and disclosure of contingent assets and liabilities at the date of the financialstatements and the reported amounts of revenues and expenses during the reporting period. Significant estimates and assumptions are used for but not limitedto establishing the allowance for doubtful accounts, valuation of inventory, depreciation, asset impairment evaluations and establishing deferred tax assetsand related valuation allowances, and stock-based compensation. Actual results could differ from those estimates. Accounts Receivable Accounts receivable, principally trade, are generally due within 30 to 90 days and are stated at amounts due from customers, net of an allowance for doubtfulaccounts. The Company performs ongoing credit evaluations and adjusts credit limits based upon payment history and the customer‘s current creditworthiness, as determined by a review of their current credit information. The Company continuously monitors aging reports, collections and payments fromcustomers and maintains a provision for estimated credit losses based upon historical experience and any specific customer collection issues that have beenidentified. While such credit losses have historically been within expectations and the provisions established, the Company cannot guarantee that the samecredit loss rates will be experienced in the future. The Company writes off accounts receivable when they become uncollectible. Inventories Inventories are stated at the lower of cost (first-in, first-out) or market and consist of raw materials, work-in process and finished goods and include purchasedmaterials, direct labor and manufacturing overhead. Management evaluates the need to record adjustments to write down inventory to the lower of cost ormarket on a quarterly basis. The Company’s policy is to assess the valuation of all inventories, including raw materials, work-in-process and finished goodsand it writes down its inventory for estimated obsolescence based upon the age of inventory and assumptions about future demand and usage. Inventoryitems used for demonstration purposes, rentals or on consignment are classified as property, plant and equipment. Property, Plant and Equipment Property, plant and equipment are recorded at cost. Minor replacements and maintenance and repair expenses are charged to expense as incurred.Depreciation of property and equipment is provided using the straight-line method over estimated useful lives ranging from 3 to 5 years. Leaseholdimprovements are amortized over the life of the lease or the useful life of the related asset, whichever is shorter. The Company‘s policy is to periodicallyevaluate the appropriateness of the lives assigned to property, plant and equipment and make adjustments if necessary. Inventory items included in property,plant and equipment are depreciated using the straight line method over estimated useful lives of 3 to 5 years. Depreciation of BoneScapel and Sonic OneORgenerators which are consigned to customers are depreciated over a 5 year period, and depreciation is charged to selling expenses. See Note 4. F-9 Revenue Recognition The Company records revenue upon shipment for products shipped F.O.B. shipping point. Products shipped F.O.B. destination points are recorded as revenuewhen received at the point of destination. Shipments under agreements with distributors are not subject to return, and payment for these shipments is notcontingent on sales by the distributor. Accordingly, the Company recognizes revenue on shipments to distributors in the same manner as with othercustomers. Service contracts and royalty income are recognized when earned. The Company generally warrantees its product for a 12 month period, andaccordingly records a related warranty reserve. Historical warranty costs have not been significant. The Company presents taxes collected from customers and remitted to governmental authorities in the consolidated statements of operations on a net basis. Long-Lived Assets The carrying values of intangible and other long-lived assets, excluding goodwill, are periodically reviewed to determine if any impairment indicators arepresent. If it is determined that such indicators are present and the review indicates that the assets will not be fully recoverable, based on undiscountedestimated cash flows over the remaining amortization and depreciation period, their carrying values are reduced to estimated fair value. Impairment indicatorsinclude, among other conditions, cash flow deficits, an historic or anticipated decline in revenue or operating profit, adverse legal or regulatorydevelopments, accumulation of costs significantly in excess of amounts originally expected to acquire the asset and a material decrease in the fair value ofsome or all of the assets. Assets are grouped at the lowest levels for which there are identifiable cash flows that are largely independent of the cash flowsgenerated by other asset groups. No such impairment was deemed to exist in fiscal 2017 and 2016. Goodwill Goodwill is not amortized. We review goodwill for impairment annually and whenever events or changes indicate that the carrying value of an asset may notbe recoverable. These events or circumstances could include a significant change in the business climate, legal factors, operating performance indicators,competition, or sale or disposition of significant assets or products. Application of this impairment test requires significant judgments, including estimationof cash flows, which is dependent on internal forecasts, estimation of the long term rate of growth for the Company’s business, the useful lives over whichcash flows will occur and determination of the Company’s weighted average cost of capital. The Company primarily utilizes the Company’s marketcapitalization and a discontinued cash flow model in determining the fair value which consists of Level 3 inputs. Changes in the projected cash flows anddiscount rate estimates and assumptions underlying the valuation of goodwill could materially affect the determination of fair value in acquisition or duringsubsequent periods when tested for impairment. The Company completed its annual goodwill impairment tests for fiscal 2017 and 2016 as of June 30th eachyear. No impairment of goodwill was deemed to exist in fiscal 2017, 2016 and 2015. Patents The cost of acquiring or processing patents is capitalized at cost. This amount is being amortized using the straight-line method over the estimated usefullives of the underlying assets, which is approximately 17 years. Patents totaled $719,136 and $604,916 at June 30, 2017 and 2016, respectively.Amortization expense for the years ended June 30, 2017, 2016 and 2015 was approximately $110,000, $94,000 and $150,000, respectively. F-10 The following is a schedule of estimated future patent amortization expense as of June 30, 2017 during the following fiscal years: 2018 $116,3752019 105,2112020 81,7822021 75,6112022 49,642Thereafter 290,515 $719,136 Income Taxes Deferred tax assets and liabilities are recognized for the future tax consequences attributable to differences between the financial statement carrying amountsof existing assets and liabilities and their respective tax bases and operating loss and tax credit carry forwards. Deferred tax assets and liabilities are measuredusing enacted tax rates expected to apply to taxable income in the years in which those temporary differences are expected to be recovered or settled. Theeffect on deferred tax assets and liabilities of a change in tax rates is recognized in income in the period that includes the enactment date. The ultimaterealization of deferred tax assets is dependent upon the generation of future taxable income in those periods in which temporary differences becomedeductible. Should management determine that it is more likely than not that some portion of the deferred tax asset will not be realized, a valuationallowance against the deferred tax asset would be established in the period such determination was made. The Company recognizes a tax benefit from an uncertain tax position only if it is more likely than not that the tax position will be sustained on examinationby the taxing authorities based on the technical merits of the position. The tax benefits recognized in the financial statements from such position aremeasured based on the largest benefit that has a greater than fifty percent likelihood of being realized upon ultimate settlement. The Company classifiesincome tax related interest and penalties as a component of income tax expense. Income (Loss) Per Share Basic income (loss) per common share (“Basic EPS”) is computed by dividing income (loss) by the weighted average number of common shares outstandingusing the treasury stock method. Diluted income (loss) per common share (“Diluted EPS”) is computed by dividing income (loss) by the weighted averagenumber of common shares and the dilutive common share equivalents and convertible securities then outstanding. The number of weighted average common shares used in the calculation of Basic EPS and Diluted EPS were as follows: For the years endedJune 30, 2017 2016 2015 Basic shares 8,398,778 7,776,949 7,580,450 Dilutive effect of stock options — — 513,669 Diluted shares 8,398,778 7,776,949 8,094,119 Excluded from the calculation of Diluted EPS are options to purchase 257,000 shares of common stock for the twelve months ended June 30, 2015. Theexcluded shares are any shares in which the average stock price for the year ended June 30 is less than the exercise price of the outstanding options in theperiod in which the Company has net income. Diluted EPS for the twelve months ended June 30, 2017 and 2016 presented is the same as Basic EPS, as theinclusion of the effect of common share equivalents then outstanding would be anti-dilutive. For this reason, excluded from the calculations of diluted EPSfor the twelve months ended June 30, 2017 and 2016 are outstanding options to purchase 1,191,236 and 1,790,224 shares, respectively. Also excluded fromthe calculation of earnings per share are the 400,000 restricted stock awards which we issued in December 2016 as none of the shares were vested as of June30, 2017. F-11 Research and Development All research and development expenses are expensed as incurred and are included in operating expenses. Advertising Expense The cost of advertising is expensed in the period the advertising first takes place. The Company incurred approximately $76,000, $386,000 and $155,000 inadvertising costs during the fiscal years ended June 30, 2017, 2016 and 2015, respectively. Advertising costs are reported in selling expenses on thestatement of operations. Depreciation Expense for Consigned Inventory The Company typically provides to its United States customers, on a consignment basis, the generators used to power its BoneScapel and SonicOne products.Title to these generators remains at all times with the Company. When these generators are deployed in the field at customer locations, the Companydepreciates these units over a five year period and charges the depreciation to selling expenses. Depreciation expense relating to consigned generators for thethree years ended June 30, 2017 was $425,000, $416,000 and $232,000, respectively. Prior to fiscal 2017, consigned units were depreciated over a three yearperiod. The impact of this change in accounting estimate was a reduction in expense of approximately $283,000 for the year ended June 30, 2017, comparedto what the expense would have been without this change. Shipping and Handling Shipping and handling fees for the fiscal years ended June 30, 2017, 2016 and 2015 were approximately $119,000, $109,000 and $62,000 respectively, andare reported as a component of net sales. Shipping and handling costs for the fiscal years ended June 30, 2017, 2016 and 2015 were approximately $337,000,$142,000 and $87,000, respectively, and are reported as a component of selling expenses. Stock-Based Compensation The Company measures compensation cost for all share based payments at fair value and recognizes the cost over the vesting period. The Company uses theBlack-Scholes method to value awards and utilizes the straight line amortization method to recognize the expense associated with the awards with gradedvesting terms. Restricted Stock AwardsThe Company measures compensation cost for all restricted stock awards at fair value and recognizes the cost over the vesting period. For awards that havemarket conditions, the Company uses the Monte Carlo valuation method to value awards and utilizes the straight line amortization method to recognize theexpense associated with the awards with graded vesting terms. Where awards have performance conditions, the Company will determine the probability ofachieving those conditions and will record compensation expense when it is probable that the conditions will be met. Recent Accounting Pronouncements In May 2014, the Financial Accounting Standards Board (the “FASB”) issued guidance on revenue from contracts with customers. The underlying principleis that an entity will recognize revenue to depict the transfer of goods or services to customers at an amount that the entity expects to be entitled to inexchange for those goods or services. The guidance provides a five-step analysis of transactions to determine when and how revenue is recognized. Othermajor provisions include capitalization of certain contract costs, consideration of time value of money in the transaction price, and allowing estimates ofvariable consideration to be recognized before contingencies are resolved, in certain circumstances. The guidance also requires enhanced disclosuresregarding the nature, amount, timing and uncertainty of revenue and cash flows arising from an entity‘s contracts with customers. This guidance permits theuse of either the retrospective or cumulative effect transition method and is effective for the Company beginning in 2019; early adoption is permittedbeginning in 2018. We have not yet selected a transition method and are currently evaluating the impact of the guidance on the Company‘s financialcondition, results of operations and related disclosures. The FASB has also issued the following additional guidance clarifying certain issues on revenue fromcontracts with customers: Revenue from Contracts with Customers - Narrow-Scope Improvements and Practical Expedients and Revenue from Contracts withCustomers - Identifying Performance Obligations and Licensing. The Company is currently in the early stages of evaluating this guidance to determine theimpact it will have on its financial statements. F-12 In August 2014, the FASB issued guidance on management‘s responsibility in evaluating whether there is substantial doubt about a company‘s ability tocontinue as a going concern and related footnote disclosures. Management will be required to evaluate, at each reporting period, whether there are conditionsor events that raise substantial doubt about a company‘s ability to continue as a going concern within one year from the date the financial statements areissued. This guidance is effective prospectively for annual and interim reporting periods beginning in 2017; implementation of this guidance did not have amaterial effect on the Company’s financial condition or results of operations. In November 2015, the FASB issued ASU 2015-17 “Balance Sheet Classification of Deferred Taxes (Topic 740)”. The amendments in this ASU requiredeferred tax liabilities and assets be classified as noncurrent in a classified statement of financial position. The amendments eliminate the guidance in Topic740 that requires an entity to separate deferred tax liabilities and assets into a current amount and a noncurrent amount in a classified statement of financialposition. The Company adopted ASU 2015-17 as of March 31, 2016 on a prospective basis in order to simplify the balance sheet classification of deferredtaxes. In February 2016, the FASB issued guidance on lease accounting requiring lessees to recognize a right-of-use asset and a lease liability for long-term leases.The liability will be equal to the present value of lease payments. This guidance must be applied using a modified retrospective transition approach to allannual and interim periods presented and is effective for the Company beginning in fiscal 2019. The Company is currently in the early stages of evaluatingthis guidance to determine the impact it will have on its financial statements. In March 2016, the FASB issued guidance on simplifying several aspects of accounting for share-based payment award transactions, including income taxconsequences, classification of awards as either equity or liabilities, and classification on the statement of cash flows. This guidance requires a mix ofprospective, modified retrospective, and retrospective transition to all annual and interim periods presented and is effective for the Company beginning infiscal 2018. The Company adopted this guidance on July 1, 2017. This guidance will be adopted by the Company on July 1, 2017 and management expectsthis to result in an increase in the Company’s deferred tax asset of approximately $2.5 million. In August 2016, the FASB issued guidance on the Statement of Cash Flows Classification of certain cash receipts and cash payments (a consensus of theEmerging Issues Task Force). This guidance addresses the following eight specific cash flow issues: Debt prepayment or debt extinguishment costs;settlement of zero-coupon debt instruments or other debt instruments with coupon interest rates that are insignificant in relation to the effective interest rateof the borrowing; contingent consideration payments made after a business combination; proceeds from the settlement of insurance claims; proceeds from thesettlement of corporate-owned life insurance policies (including bank-owned life insurance policies); distributions received from equity method investees;beneficial interests in securitization transactions; and separately identifiable cash flows and application of the predominance principle. This guidance will beeffective for the Company beginning in fiscal 2019. The Company is currently in the early stages of evaluating this guidance to determine the impact it willhave on its financial statements. In January 2017, the Financial Accounting Standards Board (the “FASB”) issued ASU No. 2017-04, Simplifying the Test for Goodwill Impairment. Under thenew standard, goodwill impairment would be measured as the amount by which a reporting unit’s carrying value exceeds its fair value, not to exceed thecarrying value of goodwill. This ASU eliminates existing guidance that requires an entity to determine goodwill impairment by calculating the implied fairvalue of goodwill by hypothetically assigning the fair value of a reporting unit to all of its assets and liabilities as if that reporting unit had been acquired ina business combination. This update is effective for annual periods beginning after December 15, 2019, and interim periods within those periods. Earlyadoption is permitted for interim or annual goodwill impairment tests performed on testing dates after January 1, 2017. The Company will apply thisguidance to applicable impairment tests after January 1, 2017. F-13 In January 2017, the FASB issued ASU No. 2017-01, Business Combinations: Clarifying the Definition of a Business (“ASU 2017-01"). ASU 2017-01clarifies the definition of a business for determining whether transactions should be accounted for as acquisitions (or disposals) of assets or businesses. ASU2017-01 is effective for annual periods and interim periods within those annual periods beginning after December 15, 2017, and early adoption is permitted.The Company is in the process of evaluating the impact of the adoption of ASU 2017-01 on its consolidated financial statements. There are no other recently issued accounting pronouncements that are expected to have a material effect on the Company’s financial position, results ofoperations or cash flows. 2. Fair Value of Financial Instruments We follow a three-level fair value hierarchy that prioritizes the inputs to measure fair value. This hierarchy requires entities to maximize the use of“observable inputs” and minimize the use of “unobservable inputs.” The three levels of inputs used to measure fair value are as follows: Level 1: Quoted prices (unadjusted) for identical assets or liabilities in active markets as of the measurement date. Level 2: Significant other observable inputs other than Level 1 prices such as quoted prices for similar assets or liabilities; quoted prices in markets that arenot active; or other inputs that are observable or can be corroborated by observable market data. Level 3: Significant unobservable inputs that reflect assumptions that market participants would use in pricing an asset or liability. At June 30, 2017 and 2016, all of our cash, trade accounts receivable and trade accounts payable were short term in nature, and their carrying amountsapproximate fair value. 3. Inventories Inventories are summarized as follows: June 30, June 30, 2017 2016 Raw material $2,409,148 $3,102,175 Work-in-process 741,994 854,631 Finished goods 3,267,232 3,101,234 6,418,374 7,058,040 Less valuation reserve 1,425,940 1,235,105 $4,992,434 $5,822,935 F-14 4. Property, Plant and Equipment Property, plant and equipment consist of the following: June 30, June 30, 2017 2016 Machinery and equipment $2,452,363 $2,128,349 Furniture and fixtures 1,406,758 1,387,883 Automobiles 22,328 22,328 Leasehold improvements 691,751 682,591 Demonstration and consignment inventory 6,951,583 5,247,946 11,524,783 9,469,097 Less: accumulated depreciation and amortization (7,794,580) (6,976,282) $3,730,203 $2,492,815 Depreciation and amortization of property, plant and equipment totaled approximately $957,000, $1,339,000 and $981,000 for the fiscal years endedJune 30, 2017, 2016 and 2015, respectively. 5. Accrued Expenses and Other Current Liabilities The following summarizes accrued expenses and other current liabilities: June 30, June 30, 2017 2016 Accrued payroll, payroll taxes and vacation 715,245 648,705 Accrued bonus 343,400 300,000 Accrued commissions 751,000 433,000 Professional fees 662,537 256,130 Litigation settlement 500,000 Deferred income 27,901 20,655 Severance 10,029 — Other 336,026 228,847 $3,346,138 $1,887,337 6. Stock-Based Compensation Plans At June 30, 2017, the Company had outstanding equity-linked grants under eight stock-based compensation plans (the “Plans”), as follows: Available Initial Expired / For Plan Shares Granted Exercised Forfeited Outstanding Issuance 2001 Employee Stock Option Plan 1,000,000 1,251,261 376,368 868,955 5,938 — 2005 Employee Equity Incentive Plan 500,000 547,125 484,250 48,925 13,950 — 2005 Non Employee Director Stock Option Plan 200,000 195,000 97,500 7,500 90,000 — 2009 Employee Equity Incentive Plan 500,000 619,925 357,227 123,100 139,598 3,175 2009 Non Employee Director Stock Option Plan 200,000 195,000 48,750 33,750 112,500 38,750 2012 Employee Equity Incentive Plan 500,000 664,000 111,250 188,250 364,500 24,250 2012 Non Employee Director Stock Option Plan 200,000 180,000 — 41,250 138,750 61,250 2014 Employee Equity Incentive Plan 750,000 480,000 — 154,000 326,000 24,000 2017 Equity Incentive Plan 750,000 — — — — 750,000 Total 1,191,236 901,425 F-15 The compensation cost that has been charged against income for these plans was $1,086,139, $1,629,644 and $1,107,250 for the fiscal years ended June 30,2017, 2016 and 2015, respectively, and is recorded in the department associated with the employee to which the grants are issued. The expense for fiscal2017 included a charge to modify certain stock options of $81,765 and a reversal of stock compensation from prior periods due to forfeitures of unvestedoptions of $625,202. As of June 30, 2017, there was approximately $5,612,949 of total unrecognized compensation cost related to non-vested share-basedcompensation arrangements to be recognized over a weighted-average period of 3.2 years, which includes $3,148,986 of unrecognized compensationexpense on restricted stock awards. Shares from option exercises may be acquired by various methods. They may be acquired by (a) cash or certified check, (b) with previously acquired shares ofcommon stock having an aggregate fair market value, on the date of exercise, equal to the aggregate exercise price of all options being exercised (providedthat such shares were not acquired less than six (6) months prior to such exercise date), (c) in certain circumstances by surrendering options to acquire sharesof common stock in exchange for the number of shares of common stock. Cash in the amount of $332,592 was received from the exercise of stock options forthe year ended June 30, 2017. The Company received 141,351 shares of common stock as payment for options exercised during the year ended June 30,2017. During the year ended June 30, 2017, the Company issued 280,200 treasury shares in connection with stock option exercises. Stock options typically expire 10 years from the date of grant and vest over service periods, which typically are 4 years. All options are granted at the price ofthe Common Stock on the NASDAQ Stock Market on the date of grant as set forth in the Plans. The fair value of each option award was estimated on the date of grant using the Black-Scholes option valuation model that uses the assumptions noted in thefollowing table. The expected volatility represents the historical price changes of the Company’s stock over a period equal to that of the expected term of theoption. The Company uses the simplified method for determining the option term. The risk-free rate was based on the U.S. Treasury yield curve in effect at thetime of grant. The expected dividend yield is based upon historical and projected dividends. The Company has historically not paid dividends, and is notexpected to do so in the near term. The weighted average fair value at date of grant for options granted during the fiscal years ended June 30, 2017, 2016 and 2015 was $4.46, $4.68 and $5.70per share, respectively. The fair value was estimated based on the weighted average assumptions of: For twelve months ended June 30, 2017 2016 2015 Risk-free interest rates 1.80% 1.71% 1.60%Expected option life in years 6.25 6.25 6.50 Expected stock price volatility 54.68% 55.41% 61.13%Expected dividend yield 0% 0% 0% F-16 A summary of option activity under the Plans as of June 30, 2017, 2016 and 2015, and changes during the years ending on those dates is presented below: Options Weighted Average Aggregate Outstanding Exercise Intrinsic Shares Price Value Outstanding as of June 30, 2014 1,663,329 3.88 $4,879,106 Vested and exercisable at June 30, 2014 967,056 3.81 $2,937,802 Granted 549,000 10.11 Exercised (579,463) 4.11 Forfeited (47,250) 7.70 Expired (28,000) 8.00 Outstanding as of June 30, 2015 1,557,616 5.80 $6,553,821 Vested and exercisable at June 30, 2015 620,256 3.19 $3,911,604 Granted 320,000 8.80 Exercised (82,737) 4.60 Forfeited (4,375) 9.23 Expired (280) 5.82 Outstanding as of June 30, 2016 1,790,224 $6.38 $1,675,072 Vested and exercisable at June 30, 2016 813,349 $3.82 $1,501,208 Granted 327,500 8.34 Exercised (527,663) 3.30 Forfeited (383,625) 8.23 Expired (15,200) 8.51 Outstanding as of June 30, 2017 1,191,236 $7.66 $2,748,956 Vested and exercisable at June 30, 2017 517,361 $6.33 $1,923,794 The total fair value of shares vested during the year ended June 30, 2017 was $1,213,325. The number and weighted-average grant-date fair value of non-vested stock options at the beginning of fiscal 2017 was 977,000 and $4.96, respectively. The number and weighted-average grant-date fair value of stockoptions which vested during fiscal 2017 was 248,625 and $4.88, respectively. The following table summarizes information about stock options outstanding and exercisable at June 30, 2017: Options Outstanding Options Exercisable Weighted Average Weighted Weighted Range of Contractual Average Average Exercise Life Exercise Exercise Prices Number (Yrs.) Price Number Price $0.85-$6.74 352,236 4.1 $4.09 313,861 $3.98 $6.75-$8.53 341,750 8.3 $7.23 85,000 $7.57 $8.54-13.89 497,250 8.4 $10.49 118,500 $11.65 1,191,236 7.1 $7.66 517,361 $6.33 Stock options are granted with exercise prices not less than the fair market value of the Company’s Common Stock, at the time of the grant, with an exerciseterm as determined by the compensation committee of the Company’s board of directors (the “Committee”) not to exceed 10 years. The Committeedetermines the vesting period for the Company’s stock options. Generally, such stock options have vesting periods of immediate to four years. Certain optionawards provide for accelerated vesting upon meeting specific retirement, death or disability criteria, and upon change of control. F-17 Restricted Stock Awards On December 15, 2016, the Company issued 400,000 shares of restricted stock to its Chief Executive Officer. These awards vest over a period of up to fiveyears, subject to meeting certain service, performance and market conditions. These awards were valued at approximately $3.4 million and compensationexpense recorded for the year ended June 30, 2017 was $488,402. The awards contain a combination of vesting terms which include time vesting,performance vesting relating to revenue achievement, and market vesting related to obtaining certain levels of Company stock prices. At June 30, 2017, theCompany has estimated that it is probable that the performance conditions will be met. The awards were valued using a Monte Carlo valuation model using astock price at the date of grant of $9.60, a term of 3 to 5 years, a risk free interest rate of 1.6% to 2.1% and a volatility factor of 66.5%. 7. Commitments and Contingencies Leases The Company has entered into several non-cancellable operating leases for the rental of certain manufacturing and office space, equipment and automobilesexpiring in various years through 2021. The principal building lease provides for a monthly rental of approximately $26,000. The Company also leasescertain office equipment and automobiles under operating leases expiring through fiscal 2018. The following is a schedule of future minimum lease payments, by year and in the aggregate, under operating leases with initial or remaining terms of oneyear or more at June 30, 2017: Operating Leases 2018 353,659 2019 21,812 2020 21,812 2021 9,225 Total minimum lease payments $406,508 Certain of the leases provide for escalation clauses, renewal options and the payment of real estate taxes and other occupancy costs. Rent expense for alloperating leases was approximately $428,000, $411,000 and $375,000 for the fiscal years ended June 30, 2017, 2016 and 2015, respectively. Purchase Commitments As of June 30, 2017, 2016, and 2015, the Company had purchase and inventory commitments totaling $2,859,718, $2,507,125 and $2,982,198, respectively. Class Action Securities Litigation On September 19, 2016, Richard Scalfani, an individual shareholder of Misonix, filed a lawsuit against the Company and its former CEO and CFO in the U.S.District Court for the Eastern District of New York, alleging violations of the federal securities laws. The complaint alleges that the Company’s stock pricewas artificially inflated between November 5, 2015 and September 14, 2016 as a result of alleged false and misleading statements in the Company’s securitiesfilings concerning the Company’s business, operations, and prospects and the Company’s internal control over financial reporting. Scalfani filed the actionseeking to represent a putative class of all persons (other than defendants, officers and directors of the Company, and their affiliates) who purchased publiclytraded Misonix securities between November 5, 2015 and September 14, 2016. Scalfani seeks an unspecified amount of damages for himself and for theputative class under the federal securities laws. On March 24, 2017, the Court appointed Scalfani and another individual Misonix shareholder, TraceyAngiuoli, as lead plaintiffs for purposes of pursuing the action on behalf of the putative class. The lead plaintiffs, on behalf of the putative class, and theCompany have reached a settlement in principle under which the Company would pay $500,000 to resolve the matter. That settlement is subject to approvalby the district court. The Company believes it has various legal and factual defenses to the allegations in the complaint, and intends to vigorously defend theaction if the settlement is not approved and finalized. The Company has accrued a liability of $500,000 as of June 30, 2017. The Company believes that itsexposure will be limited to its insurance company retention of $250,000. F-18 Former Chinese Distributor - FCPA For several months, with the assistance of outside counsel, the Company conducted a voluntary investigation into the business practices of the independentChinese entity that previously distributed its products in China and the Company’s knowledge of those business practices, which may have implicationsunder the FCPA, as well as into various internal controls issues identified during the investigation. On September 27, 2016 and September 28, 2016, the Company voluntarily contacted the SEC and the DOJ, respectively, to advise both agencies of thesepotential issues. The Company has provided and will continue to provide documents and other information to the SEC and the DOJ, and is cooperating fullywith these agencies in their ongoing investigations of these matters. Although the Company’s investigation is complete, additional issues or facts could arise which may expand the scope or severity of the potential violations. The Company has no current information derived from the investigation or otherwise to suggest that its previously reported financial statements and resultsare incorrect. At this stage, the Company is unable to predict what, if any, action the DOJ or the SEC may take or what, if any, penalties or remedial measures these agenciesmay seek. Nor can the Company predict the impact on the Company as a result of these matters, which may include the imposition of fines, civil and criminalpenalties, which are not currently estimable, as well as equitable remedies, including disgorgement of any profits earned from improper conduct andinjunctive relief, limitations on the Company’s conduct, and the imposition of a compliance monitor. The DOJ and the SEC periodically have based theamount of a penalty or disgorgement in connection with an FCPA action, at least in part, on the amount of profits that a company obtained from the businessin which the violations of the FCPA occurred. During its distributorship relationship with the prior Chinese distributor from 2010 through 2016, theCompany generated sales of approximately $8 million from the relationship. Further, the Company may suffer other civil penalties or adverse impacts, including lawsuits by private litigants in addition to the lawsuits that already havebeen filed, or investigations and fines imposed by local authorities. The investigative costs to date are approximately $2.5 million, of which approximately$2.4 million was charged to general and administrative expenses during the fiscal year ended June 30, 2017. Former Chinese Distributor – Litigation On April 5, 2017, the Company’s former distributor in China, Cicel (Beijing) Science & Technology Co., Ltd., filed a lawsuit against the Company andcertain officers and directors of the Company in the United States District Court for the Eastern District of New York, alleging that the Company improperlyterminated its contract with the former distributor. The complaint, which seeks various remedies, including compensatory and punitive damages, specificperformance and preliminary and post judgment injunctive relief, asserts various causes of action, including breach of contract, unfair competition, tortiousinterference with contract, fraudulent inducement, and conversion. The Company believes it has various legal and factual defenses to the allegations in thecomplaint, and intends to vigorously defend the action. The case is at its earliest stages; there has been no discovery and there is no trial date. Stockholder Derivative Litigation On June 6, 2017, Irving Feldbaum, an individual shareholder of Misonix, filed a lawsuit in the U.S. District Court for the Eastern District of New York. Thecomplaint alleges claims against the Company’s board of directors, its former CEO and CFO, certain of its former directors, and the Company as a nominaldefendant for alleged violations of Section 14(a) of the Securities Exchange Act of 1934 and state law claims for breach of fiduciary duty, waste of corporateassets, and unjust enrichment. The complaint alleges that the Company incurred damages as a result of alleged false and misleading statements in theCompany’s securities filings concerning the Company’s business, operations, and prospects and the Company’s internal control over financial reporting. Thecomplaint also alleges that the Company’s February 4, 2016 Proxy Statement contained false and misleading statements regarding executive compensation.The complaint seeks the recovery of damages on behalf of the Company and the implementation of changes to corporate governance procedures. On June 16,2017, Michael Rubin, another individual shareholder of Misonix, filed a case alleging similar claims in the same district court. The cases are at their earlieststages; there has been no discovery and there is no trial date. The Company is not able either to estimate the amount of potential loss it may recognize, if any,from these claims or to identify any changes in corporate governance procedures it may undertake, if any, as a result of these claims. F-19 8. Related Party Transactions Stavros G. Vizirgianakis was appointed to Misonix’s Board of Directors on May 7, 2013 and became the Company’s CEO in December 2016. AppliedBioSurgical, a company formerly owned by Mr. Vizirgianakis’ father and now owned by his brother, is an independent distributor for the Company outside ofthe United States. Set forth below is a table showing the Company’s net sales for each of the past three fiscal years and accounts receivable at June 30 for the indicated timeperiods below with Applied BioSurgical: For the years ended June 30: Applied BioSurgical 2017 2016 2015 Sales $580,888 $559,787 $540,185 Accounts receivable $192,984 $272,421 $294,683 On October 25, 2016, the Company sold 761,469 shares of Common Stock in a private placement to Stavros G. Vizirgianakis, the Company’s current ChiefExecutive Officer, at a price per share of $5.253, representing total cash proceeds to the Company of approximately $4.0 million. 9. Income Taxes Open tax years related to federal and state income tax filings are for the years ended June 30, 2014, 2015, 2016 and 2017. The Company’s net operating losscarryforwards from closed years can be adjusted by the tax authorities when they are utilized in an open year. The Company files state tax returns inCalifornia, Florida, New Jersey, New York, Pennsylvania, Texas and various other states. During the current year, the Company received notification from theInternal Revenue Service of an examination for the year ended June 30, 2015. As of June 30, 2017, no significant preliminary audit findings were received bythe Company and no reserves have been recorded. The Company’s foreign subsidiary, Misonix Ltd. filed tax returns in the United Kingdom. Open yearsrelated to the United Kingdom for filing are June 30, 2015, 2016 and 2017. As of June 30, 2017 and 2016, the Company has no material unrecognized taxbenefits and no accrued interest and penalties. Deferred income taxes reflect the net tax effects of temporary differences between the carrying amounts of assets and liabilities for financial reportingpurposes and the amounts used for income tax purposes. F-20 The tax effects of temporary differences that give rise to significant portions of the deferred tax assets and liabilities are presented below: June 30, 2017 2016 Deferred tax assets / (liabilities) Bad debt reserves $34,243 $34,151 Inventory reserves 676,733 624,808 Accruals and allowances 269,539 148,479 License fee and other income — 2,139 Net operating loss carryforwards 3,500,826 2,204,637 Tax credits 455,916 406,070 Stock based compensation 451,892 839,611 Deferred gain - HIFU and Labcaire 149,222 156,275 Amortization (594,306) (599,802)Depreciation 16,030 195,048 Other 3,182 12,004 4,963,277 4,023,420 Valuation Allowance (628,730) (628,730)Total net deferred tax assets $4,334,547 $3,394,690 Prior to June 30, 2014 and through March 31, 2015, the Company had a full valuation allowance recorded against deferred tax assets. As of the year endedJune 30, 2015, the Company reduced the valuation allowance by $5,503,417. The change in the valuation allowance includes a $1,499,297 write-off ofdeferred tax assets against its corresponding valuation allowance. The write-off primarily pertains to the loss in tax benefit for net operating losses subject tolimitations under federal tax law that precludes its utilization. In addition, during the fourth quarter of fiscal 2015, based on the Company’s consideration ofall available positive and negative evidence including achieving cumulative profitable operating performance over the prior three years and the Company’spositive outlook for taxable income in the future, the Company reevaluated its deferred tax asset. Based upon the guidance under ASC 740, the Companyconcluded that it was more likely than not that the Company would realize the benefit of such deferred tax assets. The portion of the valuation allowancerelease attributable to income in future years resulted in the recognition of a tax benefit of $2,892,000 in continuing operations in the fourth quarter of fiscal2015. The deferred tax asset will be realized against future income tax expense that would be payable in the absence of the net operating loss carryforward.The Company still maintains a full valuation allowance on all foreign net operating losses in the amount of $628,730. At June 30, 2017, the Company has a gross deferred tax asset of $4,963,277. Based upon the guidance under ASC 740, after consideration of all availablepositive and negative evidence, the Company concluded that it was more likely than not that the Company would realize the benefit of its deferred tax assets.Accordingly, the Company concluded that no valuation allowance was required at June 30, 2017. This determination was primarily based on the Company’sforecasted taxable income for future periods. The forecast of future taxable income is based on judgments which the Company has made regarding its abilityto grow revenue both domestically and internationally, its ability to control costs, its ability to introduce new products into the marketplace and its ability toachieve and maintain profitability. As of June 30, 2017, the Company had approximately $10,781,000 of U.S. federal net operating loss carryforwards which expire in tax years between 2031and 2037. Included in this amount are windfall tax benefits related to exercised stock options of approximately $2,571,000, the benefit of which will berecorded in equity when realized when the Company adopts ASU 2016-09 beginning in fiscal 2018. The Company has approximately $281,000 of researchand development tax credit carryforwards which expire in the tax years between 2026 and 2037. In addition, the Company has approximately $175,000 ofalternative minimum tax credit which has an indefinite carryforward period. F-21 Significant components of the income tax expense (benefit) attributable to continuing operations are as follows: Year Ended June 30, 2017 2016 2015 Current: Federal $— $4,962 $59,686 State 5,424 17,012 44,361 Total current 5,424 21,974 104,047 Deferred: Federal (990,016) (558,133) (2,845,039)State (38,216) (37,192) (43,640)Total deferred (1,028,232) (595,325) (2,888,679) $(1,022,808) $(573,351) $(2,784,632) The reconciliation of income tax expense (benefit) computed at the Federal statutory tax rates to income tax expense (benefit) is as follows: Year ended June 30, 2017 2016 2015 Tax at federal statutory rates $(974,308) $(646,828) $856,604 State income taxes, net of federal benefit (34,636) (13,319) 29,278 Research credit (50,000) (49,593) (70,401)Stock-based compensation 6,692 191,827 303,398 Deferred tax asset adjustments (1) — (100,939) — Valuation allowance — — (3,914,045)Travel and entertainment 34,743 35,010 21,508 Other (5,299) 10,491 (10,974) $(1,022,808) $(573,351) $(2,784,632) (1)Relates to the correction of two errors from the fiscal 2015 tax provision in fiscal 2016 as the net impactwas not material. 10. Employee Profit Sharing Plan The Company sponsors a retirement plan pursuant to Section 401(k) of the Internal Revenue Code of 1986, as amended (the “Code”) for all full-timeemployees. Participants may contribute a percentage of compensation not to exceed the maximum allowed under the Code, which was $24,000 if theemployee was over 50 years of age for the year ended June 30, 2017. The plan provides for a matching contribution by the Company of 10% of annualeligible compensation contributed by the participants based on years of service, which amounted to $57,465, $52,145 and $46,636 for the fiscal years endedJune 30, 2017, 2016 and 2015, respectively. 11. Segment Reporting Operating segments are defined as components of an enterprise about which separate financial information is available that is evaluated on a regular basisby the chief operating decision-maker (“CODM”) in deciding how to allocate resources to an individual segment and in assessing performance of thesegment. The Company has concluded that its Chief Executive Officer is the CODM as he is the ultimate decision maker for key operating decisions,determining the allocation of resources and assessing the financial performance of the Company. These decisions, allocations and assessments are performedby the CODM using consolidated financial information. Consolidated financial information is utilized by the CODM as the Company’s current productoffering primarily consists of minimally invasive therapeutic ultrasonic medical devices. The Company’s products are relatively consistent andmanufacturing is centralized and consistent across product offerings. Based on these factors, key operating decisions and resource allocations are made bythe CODM using consolidated financial data and as such the Company has concluded that it operates as one segment. F-22 Worldwide revenue for the Company’s products is categorized as follows: For the Years Ended June 30, 2017 2016 2015 Total Consumables $20,328,676 $16,091,651 $12,833,377 Equipment 6,941,287 7,021,543 9,371,201 Total $27,269,963 $23,113,194 $22,204,578 Domestic: Consumables $14,866,772 $11,277,449 $8,449,215 Equipment 1,593,999 1,809,357 2,348,705 Total $16,460,771 $13,086,806 $10,797,920 International: Consumables $5,461,904 $4,814,202 $4,384,162 Equipment 5,347,288 5,212,186 7,022,496 Total $10,809,192 $10,026,388 $11,406,658 Substantially all of the Company’s long-lived assets are located in the United States. F-23 12. Quarterly Results (unaudited) Fiscal 2017 Q1 Q2 Q3 Q4 Year Net sales $6,171,625 $6,030,380 $7,177,763 $7,890,195 $27,269,963 Cost of goods sold 1,912,007 1,818,672 2,112,099 2,374,661 8,217,439 Gross profit 4,259,618 4,211,708 5,065,664 5,515,534 19,052,524 Operating expenses: Selling expenses 3,325,687 3,271,134 3,587,859 4,036,227 14,220,907 General and administrative expenses 1,931,821 2,087,419 2,484,962 3,091,004 9,595,206 Research and development expenses 492,084 440,364 465,863 439,186 1,837,497 Total operating expenses 5,749,592 5,798,917 6,538,684 7,566,417 25,653,610 Loss from operations (1,489,974) (1,587,209) (1,473,020) (2,050,883) (6,601,086) Other income/(expense): Interest income 19 19 18 19 75 Royalty income and license fees 944,068 949,048 953,235 925,259 3,771,610 Other (1,996) (6,640) (6,940) (20,635) (36,211)Total other income 942,091 942,427 946,313 904,643 3,735,474 (Loss) from continuing operations before income taxes (547,883) (644,782) (526,707) (1,146,240) (2,865,612) Income tax (benefit) (26,000) (30,000) (219,000) (747,808) (1,022,808) Net (loss) from continuing operations $(521,883) $(614,782) $(307,707) $(398,432) $(1,842,804) Discontinued operations: Net income (loss) from discontinued operations netof income tax expense of $0,$0, $0 and $88,375,respectively 161,861 (236) 161,625 Net income from discontinued operations — — 161,861 (236) 161,625 Net (loss) $(521,883) $(614,782) $(145,846) $(398,668) $(1,681,179) Net (loss) per share from continuing operations - Basic $(0.07) $(0.07) $(0.04) $(0.05) $(0.22) Net income per share from discontinued operations -Basic — — 0.02 — 0.02 Net (loss) per share - Basic $(0.07) $(0.07) $(0.02) $(0.05) $(0.20) Net (loss) per share from continuing operations -Diluted $(0.07) $(0.07) $(0.04) $(0.05) $(0.22) Net income per share from discontinued operations -Diluted — — 0.02 — 0.02 Net (loss) per share - Diluted $(0.07) $(0.07) $(0.02) $(0.05) $(0.20) F-24 Fiscal 2016 Q1 Q2 Q3 Q4 Year Net sales $5,250,985 $6,039,355 $5,426,147 $6,396,707 $23,113,194 Cost of goods sold 1,760,699 1,957,900 1,859,749 2,062,278 7,640,626 Gross profit 3,490,286 4,081,455 3,566,398 4,334,429 15,472,568 Operating expenses: Selling expenses 2,656,280 2,991,687 3,319,385 3,665,609 12,632,961 General and administrative expenses 1,803,920 1,675,090 1,515,559 1,834,947 6,829,516 Research and development expenses 399,994 392,068 548,278 499,139 1,839,479 Total operating expenses 4,860,194 5,058,845 5,383,222 5,999,695 21,301,956 Loss from operations (1,369,908) (977,390) (1,816,824) (1,665,266) (5,829,388) Other income/(expense): Interest income 19 25 19 18 81 Royalty income and license fees 988,170 1,018,362 963,025 979,200 3,948,757 Other (6,021) (5,413) (5,464) (4,980) (21,878)Total other income 982,168 1,012,974 957,580 974,238 3,926,960 (Loss) from continuing operations before income taxes (387,740) 35,584 (859,244) (691,028) (1,902,428) Income tax (benefit) (168,000) (139,000) (15,000) (251,351) (573,351) Net (loss) from continuing operations $(219,740) $174,584 $(844,244) $(439,677) $(1,329,077) Discontinued operations: Net income (loss) from discontinued operations net of income tax expense of $0,$0, $0 and $88,375,respectively — — 165,000 (8,069) 156,931 Net income from discontinued operations — — 165,000 (8,069) 156,931 Net (loss) $(219,740) $174,584 $(679,244) $(447,746) $(1,172,146) Net (loss) per share from continuing operations - Basic $(0.03) $0.02 $(0.11) $(0.06) $(0.17) Net income per share from discontinued operations -Basic — — 0.02 — 0.02 Net (loss) per share - Basic $(0.03) $0.02 $(0.09) $(0.06) $(0.15) Net (loss) per share from continuing operations -Diluted $(0.03) $0.02 $(0.11) $(0.06) $(0.17) Net income per share from discontinued operations -Diluted — — 0.02 — 0.02 Net (loss) per share - Diluted $(0.03) $0.02 $(0.09) $(0.06) $(0.15) F-25 Schedule II Additions Balance at charged Balance at beginning to cost and end of Description of period expenses (Deductions) period Allowance for doubtful accounts Yearsended June 30: 2017 $96,868 $— $— $96,868 2016 $126,868 $(30,000)(A) $— $96,868 2015 $136,868 $(10,000)(A) $— $126,868 (A)Reduction in allowance for doubtful accounts due to adjustment in reserve balance. Additions Balance at charged(credited) Balance at beginning to cost and end of Description of period expenses (Deductions) period Deferred tax valuation allowance Yearended June 30: 2017 $628,730 — — $628,730 2016 $628,730 $— $— $628,730 2015 $6,132,147 $(1,111,693) $(4,391,724)(A) $628,730 (A)Reduction in deferred tax valuation allowance due to reevaluation of deferred tax assets. F-26 EXHIBIT INDEX Exhibit No. Description 21 Subsidiaries of the Company. 23 Consent of Grant Thornton LLP. 31.1 Rule 13a-14(a)/15d-14(a) Certification. 31.2 Rule 13a-14(a)/15d-14(a) Certification. 32.1 Section 1350 Certification. 32.2 Section 1350 Certification. 101.INS XBRL Instance Document 101.SCH XBRL Taxonomy Extension Scheme Document 101.CAL XBRL Taxonomy Extension Calculation Linkbase Document 101.DEF XBRL Taxonomy Extension Definition Linkbase Document 101.LAB XBRL Taxonomy Extension Label Linkbase Document 101.PRE XBRL Taxonomy Extension Presentation Linkbase Document Exhibit 21 Subsidiaries of the Company 1. Misonix Limited, a United Kingdom corporation 2. Fibra-Sonics (NY) Inc., a New York corporation 3. Hearing Innovations, Incorporated, a Delaware corporation Exhibit 23 CONSENT OF INDEPENDENT REGISTERED PUBLIC ACCOUNTING FIRM We have issued our reports dated August 24, 2017, with respect to the consolidated financial statements, schedule and internal control over financialreporting included in the Annual Report of MISONIX INC. on Form 10-K for the year ended June 30, 2017. We consent to the incorporation by reference ofsaid reports in the Registration Statements of MISONIX INC. on Forms S-8 (File No. 333-203944, File No. 333-188554, File No. 333-165088, File No. 333-130874, File No. 333-63166, File No. 333-78795, File No. 333-18907, File No. 333-73924 and File No. 333-219348). /s/ GRANT THORNTON LLP Boston, MassachusettsAugust 24, 2017 Exhibit 31.1 CERTIFICATIONS I, Stavros G. Vizirgianakis, certify that: 1. I have reviewed this annual report on Form 10-K of MISONIX, 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 thestatements 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 financialcondition, 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(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined inExchange 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)), forthe registrant and have: (a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensurethat 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, toprovide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes inaccordance 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 ofthe 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 fiscalquarter (the registrant’s fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, theregistrant’s internal control over financial reporting; and 5. The registrant’s other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to theregistrant’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 toadversely 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 overfinancial reporting. Date: August 24, 2017 By:/s/ Stavros G. Vizirgianakis Stavros G. Vizirgianakis Chief Executive Officer Exhibit 31.2 CERTIFICATIONS I, Joseph P. Dwyer, certify that: 1. I have reviewed this annual report on Form 10-K of MISONIX, 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 thestatements 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 financialcondition, 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(s) and I are responsible for establishing and maintaining disclosure controls and procedures (as defined in ExchangeAct 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 registrantand have: (a) Designed such disclosure controls and procedures, or caused such disclosure controls and procedures to be designed under our supervision, to ensurethat 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, toprovide reasonable assurance regarding the reliability of financial reporting and the preparation of financial statements for external purposes inaccordance 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 ofthe 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 fiscalquarter (the registrant's fourth fiscal quarter in the case of an annual report) that has materially affected, or is reasonably likely to materially affect, theregistrant's internal control over financial reporting; and 5. The registrant's other certifying officer(s) and I have disclosed, based on our most recent evaluation of internal control over financial reporting, to theregistrant'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 toadversely 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 overfinancial reporting. Date: August 24, 2017 By:/s/ Joseph P. Dwyer Joseph P. Dwyer Chief Financial Officer Exhibit 32.1 CERTIFICATION PURSUANT TO 18 U.S.C. SECTION 1350, AS ADOPTED PURSUANT TO SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002 In connection with the Annual Report of MISONIX, INC. (the "Company") on Form 10-K for the period ended June 30, 2017 as filed with the Securities andExchange Commission on the date hereof (the "Report"), I, Stavros G. Vizirgianakis, Chief Executive Officer of the Company, certify, pursuant to 18 U.S.C.ss. 1350, as adopted pursuant to ss. 906 of the Sarbanes-Oxley Act of 2002, that: (1) The Report fully complies with the requirements of section 13(a) or 15(d) of the Securities Exchange Act of 1934; and (2) The information contained in the Report fairly presents, in all material respects, the financial condition and result of operations of the Company. Date: August 24, 2017 By:/s/ Stavros G. Vizirgianakis Stavros G. Vizirgianakis Chief Executive Officer A signed original of this written statement required by Section 906, or other document authenticating, acknowledging, or otherwise adopting the signaturethat appears in typed form within the electronic version of this written statement required by Section 906, has been provided to MISONIX, INC. and will beretained by MISONIX, INC. and furnished to the Securities and Exchange Commission or its staff upon request. Exhibit 32.2 CERTIFICATION PURSUANT TO 18 U.S.C. SECTION 1350, AS ADOPTED PURSUANT TO SECTION 906 OF THE SARBANES-OXLEY ACT OF 2002 In connection with the Annual Report of MISONIX, INC. (the "Company") on Form 10-K for the period ended June 30, 2017 as filed with the Securities andExchange Commission on the date hereof (the "Report"), I, Joseph P. Dwyer, Chief Financial Officer of the Company, certify, pursuant to 18 U.S.C. ss. 1350,as adopted pursuant to ss. 906 of the Sarbanes-Oxley Act of 2002, that: (1) The Report fully complies with the requirements of section 13(a) or 15(d) of the Securities Exchange Act of 1934; and (2) The information contained in the Report fairly presents, in all material respects, the financial condition and result of operations of the Company. Date: August 24, 2017 By:/s/ Joseph P. Dwyer Joseph P. Dwyer Chief Financial Officer A signed original of this written statement required by Section 906, or other document authenticating, acknowledging, or otherwise adopting the signaturethat appears in typed form within the electronic version of this written statement required by Section 906, has been provided to MISONIX, INC. and will beretained by MISONIX, INC. and furnished to the Securities and Exchange Commission or its staff upon request.
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