PMI on NYSE

Picard Medical, Inc.

Picard Medical, Inc. is an American surgical and medical instruments and apparatus company.1 It is headquartered in Tucson, Arizona.1 Its shares trade on NYSE under the symbol PMI.1

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Last updated Oct 20, 2026.

Overview

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  • TickerPMI on NYSE1
  • IndustrySurgical & Medical Instruments & Apparatus1
  • HeadquartersTucson, Arizona1
  • Incorporated inDE2
  • Business address1992 E. Silverlake Rd., Tucson, Az 857132
  • Filer category, Emerging growth company2

Picard Medical, Inc. ("PMI") was incorporated in the state of Delaware on April 8, 2021. Unless the context requires otherwise, in this Annual Report, the terms "we," "us," "our," the "Company," "Picard," the "Registrant," and similar references refer to the combined operations of PMI and its consolidated subsidiaries and affiliates, including SynCardia Systems, LLC ("SynCardia").3 From its latest annual report

Financials

From the company’s reports to the SEC. Every number links to the filing it came from.

Key numbers, fiscal 2025

-4.1%Gross margin4
-268.4%Operating margin4
-546.6%Net margin4
12.5%Revenue growth, 20254
-712.6%Return on equity4

What sells

Revenue by product, business segment and region, as the company reports it to the SEC.

Products and services

Product brought in 96% of the revenue Picard Medical, Inc. broke down this way in fiscal 2025.

  1. Product$4.7M496%up 12% from 2024
  2. Rentals$194.0K44%up 42% from 2024
Products and services by year
Products and services20242025
Product$4.3M$4.7M
Rentals$137.0K$194.0K

Where the money goes

Where each dollar of revenue went, fiscal 2025

  • Cost of revenue28¢$5.1M
  • Research and development17¢$3.0M
  • Selling, general and admin55¢$10.0M
  • Income tax0¢$35.0K

Out of $4.9M in revenue.4 The company lost money this year.

Financial statements

Revenue4$4.9M in 2025+13% since 2024
0$2.0M$4.0M$6.0M2024: $4.4M$4.4M20242025: $4.9M$4.9M2025+13%
Gross profit4-$204.0K in 2025+82% since 2024
-$300.0K-$200.0K-$100.0K02024: -$112.0K-$112.0K20242025: -$204.0K-$204.0K2025+82%
Operating income4-$13.3M in 2025−3% since 2024
-$15.0M-$10.0M-$5.0M02024: -$13.7M-$13.7M20242025: -$13.3M-$13.3M2025−3%
Net income4-$27.0M in 2025+28% since 2024
-$30.0M-$20.0M-$10.0M02024: -$21.1M-$21.1M20242025: -$27.0M-$27.0M2025+28%

Every line of the income statement as filed: the last 2 fiscal years, latest first.4

Period ending2025-12-312024-12-31
Revenues$4.9M$4.4M
Cost of revenues$5.1M$4.5M
Gross loss-$204.0K-$112.0K
Research and development$3.0M$3.4M
Selling, general and administrative$10.0M$10.2M
Total operating expenses$13.1M$13.6M
Operating loss-$13.3M-$13.7M
Derivative loss-$7.0M-$4.3M
Interest expense-$5.4M-$3.1M
Change in fair values of senior secured note and warrant liabilities$1.0M$0
Financing charges-$2.3M$0
Other expense, net-$13.7M-$7.4M
Loss before income taxes-$27.0M-$21.1M
Provision (benefit) for income taxes$35.0K-$15.0K
Net loss-$27.0M-$21.1M
Undeclared Series A-1 preferred dividends$0-$2.7M
Net loss attributable to common stockholders-$27.0M-$23.7M
Net loss per sharebasic and diluted (in dollars per share)-$0.75-$2.99
Weighted average common shares outstandingbasic and diluted (in shares)36.2M shares7.9M shares
Foreign currency translation adjustments, net of tax-$50.0K-$15.0K
Comprehensive loss-$27.1M-$21.1M

Compare Picard Medical, Inc. with another company

Corporate structure

Picard Medical, Inc. sits at the top of its group. 1 entity, 1 country on record. Switch between the flow chart and the network, and select any entity to see its details.

Major holders of Picard Medical, Inc.

  • Hudson Bay Capital Management LP Filed SCHEDULE 13G/A on Picard Medical, Inc., latest Aug 7, 2026 (2 filings since Feb 11, 2026)
  • VERSA CAPITAL FUND III, L.P. Filed SCHEDULE 13G/A on Picard Medical, Inc., latest Jun 5, 2026 (2 filings since Nov 13, 2025)
  • Picard Medical, Inc. Tucson, Arizona

Built from major holders from Schedules 13D and 13G. Each entity in the chart links to its source.

What it owns

What Picard Medical, Inc. reports owning in its annual reports to the SEC: buildings, land and equipment, real estate and locations, investments, intangible assets and inventory, at the end of its latest fiscal year and a year before.

Property and equipment

ItemLatestA year beforeChange
Property and equipment, before depreciation$782.0K4 Dec 31, 2025$750.0K4 Dec 31, 2024+4.3%
Accumulated depreciation$599.0K4 Dec 31, 2025$523.0K4 Dec 31, 2024+14.5%
Property and equipment, net$183.0K4 Dec 31, 2025$227.0K4 Dec 31, 2024−19.4%
Finance-lease assets$152.0K4 Dec 31, 2025$177.0K4 Dec 31, 2024−14.1%
Operating-lease assets (leased space)$363.0K4 Dec 31, 2025$700.0K4 Dec 31, 2024−48.1%

Investments

ItemLatestA year beforeChange
Cash and cash equivalents$7.5M4 Dec 31, 2025$96.0K4 Dec 31, 2024+7661.5%

Intangibles and goodwill

ItemLatestA year beforeChange
Goodwill$615.0K4 Dec 31, 2025$615.0K4 Dec 31, 20240%
Intangible assets, net (excluding goodwill)$509.0K4 Dec 31, 2025$596.0K4 Dec 31, 2024−14.6%
Finite-lived intangibles, gross$880.0K4 Dec 31, 2025$880.0K4 Dec 31, 20240%
Accumulated amortization$371.0K4 Dec 31, 2025$284.0K4 Dec 31, 2024+30.6%
Finite-lived intangibles, net$509.0K4 Dec 31, 2025$596.0K4 Dec 31, 2024−14.6%

Inventory

ItemLatestA year beforeChange
Inventory, total$7.3M4 Dec 31, 2025$8.1M4 Dec 31, 2024−10.0%
Raw materials$6.1M4 Dec 31, 2025$6.3M4 Dec 31, 2024−3.1%
Work in process$2.5M4 Dec 31, 2025$2.8M4 Dec 31, 2024−8.4%
Finished goods$1.5M4 Dec 31, 2025$1.4M4 Dec 31, 2024+2.4%

Properties, in its own words

As of December 31, 2025, the Company does not own any real property. The Company’s offices and primary operating facility are located at 1992 E. Silverlake Road, Tucson, Arizona, which the Company leases.

The facility consists of approximately 34,034 square feet and serves as the Company’s corporate headquarters and primary operating location, supporting manufacturing operations, research and development activities, quality and regulatory functions, and administrative offices. The Company believes that this facility is suitable and adequate for its current operations and expected near-term growth. The lease for the facility expires on January 31, 2027.

The rest of Item 2

The Company’s manufacturing and quality operations conducted at this facility are subject to regulatory oversight applicable to medical device manufacturers, including compliance with the FDA’s Quality System Regulation and other applicable federal, state, and local regulatory requirements. Operations at this facility are also subject to standard environmental and safety regulations. The Company is not aware of any material environmental issues affecting the use of this facility.

The Company does not own or lease any properties outside of the United States, and the facility described above represents the primary location from which the Company conducts its operations.

Item 2 of the 10-K filed Mar 30, 2026.3

Leadership

Who has led Picard Medical, Inc., and when. Pick a name to see everywhere that person has worked.

Chief financial officer

  1. Bernard Skaggs2025–now

Chief operating officer

  1. Matt Schuster2025–now
Board members and other officers (4)

Timeline

  1. Oct 13, 20268-K Bylaws or fiscal year changed13
  2. Oct 6, 20268-K New debt or obligation; Unregistered sale of shares14
  3. Aug 20, 20268-K Regulation FD disclosure15
  4. Jul 27, 20268-K Listing notice or transfer; Other events16
  5. Jul 22, 20268-K Bylaws or fiscal year changed; Other events17
  6. Jul 21, 20268-K Shareholder vote18
  7. Jul 13, 20268-K Other events19
  8. Jul 7, 20268-K Executive or director change20
  9. Jul 2, 20268-K Other events21
  10. Jul 2, 20268-K Other events22
  11. Jun 29, 20268-K Executive or director change23
  12. Jun 24, 20268-K Executive or director change24
  13. Aug 28, 2025New chief executive Patrick Nj Schnegelsberg becomes CEO7

Calendar

Coming up

  1. Nov 13, 2026Reports results for the quarter ending Sep/2026 A year earlier it reported ($9.50) a share, on Nov 14, 2025.25

When it reported results

  1. May 21, 2026Reported quarterly or annual results26
  2. Apr 22, 2026Reported quarterly or annual results27
  3. Mar 25, 2026Reported quarterly or annual results28
  4. Nov 14, 2025Reported quarterly or annual results29

Upcoming dates from Nasdaq's calendar; past results from the company's 8-K filings (Item 2.02). The full markets calendar

Filings

136 filings to the SEC since October 2021: 2 annual reports, 4 quarterly reports, 44 major events, 10 insider forms, 4 large holders, 72 other. The latest 20:

  1. Oct 13, 20268-K EDGAR
  2. Oct 6, 20268-K EDGAR
  3. Aug 20, 20268-K EDGAR
  4. Aug 19, 202610-Q EDGAR
  5. Aug 17, 2026NT 10-Q EDGAR
  6. Aug 7, 2026SCHEDULE 13G/A EDGAR
  7. Jul 27, 20268-K EDGAR
  8. Jul 22, 20268-K EDGAR
  9. Jul 21, 20268-K EDGAR
  10. Jul 16, 2026DEFA14A EDGAR
  11. Jul 13, 20268-K/A EDGAR
  12. Jul 8, 2026DEFA14A EDGAR
  13. Jul 7, 20268-K/A EDGAR
  14. Jul 2, 2026425 EDGAR
  15. Jul 2, 20268-K EDGAR
  16. Jul 2, 2026425 EDGAR
  17. Jul 2, 20268-K EDGAR
  18. Jun 29, 20268-K EDGAR
  19. Jun 29, 2026DEF 14A EDGAR
  20. Jun 24, 20268-K EDGAR

The 136 filings since October 2021 can be filtered by form type and year here when JavaScript is on.

Every filing from the last five years, summarized. The full record is on SEC EDGAR.

Major holders

Investors who own more than 5% of the shares must tell the SEC: a 13D if they may seek to influence the company, a 13G if they hold passively.

Executive pay

What the company paid its top executives, from the summary compensation table in its proxy statement. Total pay includes salary, bonus, stock and option awards and other pay, as the company valued them.

YearExecutiveAgeSalaryTotal pay
2025Patrick NJ Schnegelsberg,$400.0K32
2025Matt Schuster,45$220.0K32
2025Bernard Skaggs,$200.0K32
2024Former ChiefExecutive Officer$400.0K$1.6M32
2024Chief Operating Officer$220.0K$529.4K32
2024Former Chief Financial Officer$200.0K$472.6K32

SEC filer profile

How Picard Medical, Inc. is registered with the Securities and Exchange Commission, from its EDGAR record and the cover page of its latest annual report.

  • Name on EDGARPicard Medical, Inc.1
  • CIK0002030617
  • Employer ID (EIN)86-32128943
  • Filer statusNon-accelerated filer an emerging growth company; a smaller reporting company; not a shell company3
  • Incorporated inDelaware3
  • Fiscal year endsDecember 311
  • Industry code (SIC)3841 Surgical & Medical Instruments & Apparatus1
  • SEC reviewing officeOffice of Industrial Applications and Services, Division of Corporation Finance1
  • Business address1992 E. Silverlake Rd., Tucson, AZ 857131
  • Phone520-308-07961
  • Shares outstanding2,338,634 as of Aug 18, 20266
  • Public float$130.8M as of Jun 30, 20253
  • AuditorMaloneBailey, LLP, Houston, Texas PCAOB ID 206; no auditor attestation of internal control over financial reporting3
  • On EDGAR sinceAug 23, 20241
  • Filings136 in all: 8-K (42), CORRESP (17), UPLOAD (10), S-1/A (9), 3 (7), 10-Q (4), EFFECT (4), S-1 (4)1
    All 29 form types

    3/A (3), DEF 14A (3), DRS/A (3), PRE 14A (3), 144 (2), 424B3 (2), 424B4 (2), 425 (2), 8-K/A (2), DEFA14A (2), DRS (2), FWP (2), SCHEDULE 13G (2), SCHEDULE 13G/A (2), 10-K (1), 10-K/A (1), 8-A12B (1), CERT (1), DEFR14A (1), NT 10-Q (1), S-8 (1)

  • Latest filingsAnnual report (10-K) Mar 30, 2026
    Quarterly report (10-Q) Aug 19, 2026
    Proxy statement (DEF 14A) Jun 29, 2026
    Latest 8-K (8-K) Oct 13, 2026

Securities registered for trading

ClassSymbolExchange
Common stock, par value $0.0001 per sharePMINYSE

From the cover page of the 10-K filed Mar 30, 2026 (Section 12(b) of the Exchange Act).3

Risk factors and legal proceedings

The risks Picard Medical, Inc. names in Item 1A of its 10-K filed Mar 30, 2026: 53 risks under these headings, as written.3

  • Risks Related to Our Business and Industry
  • We have a history of significant losses. If we do not achieve and sustain profitability, our financial condition could suffer.
  • All of our revenue is generated from a limited number of products, and any decline in the sales of these products or failure to gain market acceptance of these products will negatively impact our business.
  • The manufacturing process of the SynCardia TAH requires highly specialized knowledge and operator skills, which could affect our ability to manufacture the SynCardia TAH on a timely basis. If we are unable to manufacture the SynCardia TAH on a timely basis consistent with our quality standards, our results of operations will be adversely impacted.
  • We rely on specialized suppliers and service providers for components of the SynCardia TAH and do not have second-source suppliers for the majority of components.
  • The future demand for our current products and future products is unproven. Our current products and future products may not be accepted by hospitals, surgeons or patients, and may not become commercially successful.
  • Once SynCardia TAH has been proven either safe and with probable benefit (through an approved HDE) or safe and effective (through an approved PMA), If SynCardia is unable to educate physicians on the safe and effective use of the SynCardia TAH and the procedure to implement the SynCardia TAH, we may be unable to achieve our expected growth.
  • If we fail to develop and retain a direct sales force and effective network of international distributors, we may be unable to achieve expected growth targets and our business could suffer.
  • Reliance on distributors and third parties to market and sell our products could negatively impact our business.
  • We operate in a market segment that is subject to rapid technological change. If our competitors are able to develop and market technologies or products that are safer, more effective, less costly, easier to use or otherwise more attractive than our products, our business will be adversely impacted.
  • SynCardia has significant customer concentrations, and economic difficulties or changes in the purchasing policies or patterns of our key customers could have a significant impact on our business and operating results. We have no long-term exclusive agreements with our customers and, as a result, generally operate on an invoice and purchase order basis to meet our customers’ needs.
  • Our future success depends on our ability to develop, receive regulatory approval (including long term indication) for, and introduce new products or product enhancements that will be accepted by the market in a timely manner.
The other 42 risks
  • If we are unable to successfully complete the pre-clinical studies or clinical trials necessary to support premarket approval applications or PMA supplements, our ability to obtain approvals for new products will be limited.
  • Premarket approvals for our therapeutic medical devices could be denied or significantly delayed.
  • We are subject to extensive post-marketing regulation by the FDA and comparable authorities in other jurisdictions, which could impact the sales and marketing of our products and could cause us to incur significant costs to maintain compliance. In addition, we may become subject to additional regulation in other jurisdictions as we increase our efforts to market and sell our products outside of the U.S.
  • If third-party payors do not continue to provide adequate coverage and reimbursement for the use of our products, it is unlikely that our products will be widely used, and our revenues will be negatively impacted.
  • Our manufacturing operations, research and development activities, and corporate headquarters are currently based at a single location, which may subject us to a variety of risks.
  • Product liability claims could damage our reputation or adversely affect our business.
  • Product deficiencies could result in field actions, recalls, substantial costs and write-downs; these could also lead to the delay or termination of planned studies or future clinical trials, if any, and harm our reputation and our business and financial results.
  • Any claims related to improper handling, storage or disposal of hazardous chemicals and biomaterials could be time-consuming and costly to address.
  • Our international operations subject us to certain operating risks, which could adversely impact our results of operations and financial condition.
  • Changes in U.S. and international trade policies, particularly with respect to China, may adversely impact our business and operating results.
  • We are subject to credit risk from our accounts receivable related to our product sales, which include sales within foreign countries that have recently experienced economic turmoil.
  • Changes in U.S. and foreign tax laws could have a material adverse effect on our business, cash flow, results of operations or financial conditions.
  • Our ability to use net operating loss carryforwards and certain other tax attributes may be subject to limitations.
  • Our ability to maintain our competitive position depends on our ability to attract and retain highly qualified personnel.
  • If we acquire other companies or businesses, we will be subject to risks that could hurt our business.
  • Failure to protect our information technology infrastructure against cyber-based attacks, network security breaches, service interruptions, or data corruption could significantly disrupt our operations and adversely affect our business and operating results.
  • Failure to protect the product and patient from cybersecurity risks associated with using the device could endanger patient safety and our ability to market the product.
  • The demand for total artificial hearts depends on a variety of factors. In particular, medical advances, that would either provide a better alternative or replace the use of a SynCardia TAH, which would ultimately result in the demand for SynCardia TAHs to decrease and would adversely affect our business, prospects, financial condition, and operating results.
  • Risks Related to Regulation of Our Industry
  • The off-label use or misuse of our products may harm our image in the marketplace, result in injuries that lead to product liability suits, which could be damaging to our reputation and costly to our business, and/or result in costly investigations and regulatory agency sanctions or even civil or criminal penalties if we are deemed to have engaged in such promotion.
  • We are required to comply with medical device reporting, or MDR, requirements and must report certain malfunctions, deaths, and serious injuries associated with our products, which can result in voluntary corrective actions or agency enforcement actions.
  • Our employees, independent contractors, principal investigators, consultants, commercial partners, and suppliers may engage in misconduct or other improper activities, including non-compliance with regulatory standards and requirements.
  • We are subject to various federal, state, and foreign healthcare laws and regulations, and a finding of failure to comply with such laws and regulations could have a material adverse effect on our business.
  • The SynCardia TAH is currently approved in the U.S. for bridge to transplant indications. We plan to seek approval for long-term indications of 2 years, or more, in the future. If we do not receive that approval within the next year, we may need to undertake additional clinical trials, which could cost significant funds and adversely affect our business.
  • In Europe, we voluntarily withdrew our CE certificate under CE MDD in 2022 and terminated our relationship with our CE notified body to migrate from CE MDD to CE MDR, and failure to reinstate our CE certificate under CE MDR or could have a material adverse effect on our business.
  • Prior weaknesses in our CE MDD regulatory regime and compliance with developing European Union medical device regulations, including the CE MDD, may limit our ability to market or sell products in European markets or to introduce new products into European markets.
  • Risks Related to Our Intellectual Property
  • Many aspects of the SynCardia TAH are no longer protected by patents, and we may be unable to, in the long term, protect our products from competition through other means.
  • The medical device industry is characterized by extensive patents and other intellectual property litigation, and we could become subject to litigation that could be costly, result in the diversion of management’s attention, require us to pay significant damages or royalty payments, or prevent us from marketing and selling our existing or future products.
  • If we cease our commercial ties or contractual arrangements with either Bimba or Heitek Automation, we will be required to source crucial components for the C2 and Freedom Driver from an alternative supplier, which could have a negative impact on our business and operations if one is not found.
  • We may be subject to claims that we or our employees have inadvertently or intentionally used or disclosed trade secrets or other proprietary information of former employers of our employees.
  • Risks Related to Ownership of Our Securities
  • Our share price may be volatile, and purchasers of our securities could incur substantial losses.
  • Our independent registered public accounting firm has included an explanatory paragraph relating to our ability to continue as a going concern in its report on our audited financial statements included in this Registration Statement for the fiscal year ended December 31, 2025.
  • We are a “controlled company” within the meaning of the applicable rules of NYSE and, as a result, qualify for exemptions from certain corporate governance requirements. We rely on these exemptions while we search for candidates to serve as independent directors, and accordingly, our stockholders will not have the same protections afforded to stockholders of companies that are subject to such requirements.
  • We do not intend to pay cash dividends for the foreseeable future. As a result, your ability to achieve a return on your investment will depend on appreciation in the market price of our common stock.
  • Future issuances of common stock, or the perception that future issuances may occur, may cause the market price of common stock to decline, regardless of our operating performance.
  • The exercise of outstanding warrants and stock options, and the sale of common stock upon exercise thereof, may adversely affect the trading price of our securities.
  • We continue to incur increased costs and become subject to additional regulations and requirements as a result of becoming a public company, and our management will continue to be required to devote substantial time to compliance matters, which could lower our profits or make it more difficult to run our business. Compliance failures could adversely affect our business, results of operations, and financial condition.
  • We are an “emerging growth company” and a “smaller reporting company” within the meaning of the Securities Act, and we take advantage of certain exemptions from disclosure requirements available to emerging growth companies and/or smaller reporting companies, which could make our securities less attractive to investors and may make it more difficult to compare our performance with that of other public companies.
  • We could be subject to securities class action or derivative litigation.
  • If we are unable to implement and maintain effective internal control over financial reporting, investors may lose confidence in the accuracy and completeness of our financial reports and the market price of common stock may decrease.
  • An active trading market may not develop or be sustained.
  • If securities or industry analysts do not publish research, or publish inaccurate or unfavorable research, about our business, our common stock share price and trading volume could decline.
  • Our Charter designates specific courts as the exclusive forum for substantially all stockholder litigation matters, which could limit the ability of our stockholders to obtain a favorable forum for disputes with us or our directors, officers or employees.

Legal proceedings

PMI is subject from time to time to various claims, lawsuits, and other legal and administrative proceedings (including those described below). Some of these claims, lawsuits and other proceedings may involve highly complex issues that are subject to substantial uncertainties and could result in damages, fines and penalties, non-monetary sanctions, or other relief. The Company intends to recognize provisions for claims or pending litigation when it determines that an unfavorable outcome is probable, and the amount of loss can be reasonably estimated. Due to the inherent uncertain nature of litigation, the ultimate outcome or actual cost of settlement may materially vary from estimates. For additional information, see “Risk Factors – Litigation Related to Trading of Our Securities.”

On February 2, 2026, a putative securities class action captioned Louie v. Picard Medical, Inc., et al., Case No. 5:26-CV-01024, was filed in the United States District Court for the Northern District of California, San Jose Division. The complaint names PMI as a defendant, along with certain of its current and former officers and directors and other third parties, and purports to assert claims under Sections 10(b) and 20(a) of the Exchange Act and Rule 10b‑5 promulgated thereunder. The putative class period alleged is from September 2, 2025, through October 31, 2025. The complaint generally alleges, among other things, that defendants made materially false or misleading statements or omissions in connection with the Company’s initial public offering and subsequent public disclosures, and that the Company’s securities were affected by social‑media‑based promotion activity. The complaint seeks unspecified compensatory damages, attorneys’ fees and costs, and other relief.

The opening of Item 3, Legal Proceedings.3

Sources

The numbers on this page point here. Each one links to the record it came from.

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    SEC EDGAROther events
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