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Picard Medical (NYSE: PMI) grows 2025 revenue and repairs balance sheet

Filing Impact
(High)
Filing Sentiment
(Neutral)
Form Type
8-K

Rhea-AI Filing Summary

Picard Medical furnished an earnings presentation covering 2025 results and a strategic update for its SynCardia total artificial heart platform. Revenue rose 12.50% to $4.94 million, driven by 33.49% U.S. growth, which accounted for 88.25% of revenue. The company completed an IPO, raising $35.55 million, and used the funds to repay legacy debt, support operations, and cover transaction costs. Net loss was about $27.00 million, but non-cash and financing items reduced operating cash burn to $15.67 million (GAAP), with a non-GAAP normalized burn of $11.04 million. Cash increased to $11.451 million and notes payable fell sharply, moving stockholders’ equity from a $(44.00) million deficit to positive $3.789 million. Picard highlighted ongoing development of the fully implantable Emperor Total Artificial Heart, next-generation Unicorn portable driver, manufacturing optimization, and regulatory expansion as key priorities for 2026.

Positive

  • Balance sheet transformation: 2025 IPO and financing lifted stockholders’ equity from a roughly $(44.00) million deficit to positive $3.789 million, while notes payable fell from $19.976 million to $6.448 million and derivative liabilities were eliminated.
  • Revenue and U.S. growth: Total revenue increased 12.50% to $4.94 million in 2025, with U.S. revenue up 33.49% and representing 88.25% of total sales, indicating strengthening adoption in the company’s core, higher-margin market.

Negative

  • High losses and cash burn: Picard reported an approximate $27.00 million net loss for 2025, with GAAP net cash used in operations of $15.67 million and a normalized non-GAAP operating cash burn of $11.04 million, underscoring ongoing dependence on external funding.

Insights

Picard pairs double-digit revenue growth with a major balance sheet reset but remains early-stage and loss-making.

Picard Medical reported 2025 revenue of $4.94 million, up 12.50%, with U.S. sales growing 33.49% and contributing 88.25% of revenue. This shows growing adoption of the SynCardia Total Artificial Heart in its highest-margin geography, off a small base.

The company completed an IPO, raising $35.55 million. It used proceeds to repay legacy debt and fund operations, cutting notes payable from $19.976 million to $6.448 million and eliminating a derivative liability, which turned stockholders’ equity from a $(44.001) million deficit to positive $3.789 million.

Despite this balance sheet improvement, Picard still posted an approximate $27.00 million net loss and GAAP operating cash use of $15.67 million. The business remains dependent on external capital while investing in its Emperor fully implantable artificial heart, Unicorn driver, and manufacturing moves that aim to improve margins over time.

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UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 8-K

 

CURRENT REPORT

PURSUANT TO SECTION 13 OR 15(d) OF THE

SECURITIES EXCHANGE ACT OF 1934

 

Date of Report (Date of earliest event reported): March 25, 2026

 

Picard Medical, Inc.

(Exact name of registrant as specified in its charter)

 

Delaware   001-42801   86-3212894

(State or other jurisdiction

of incorporation)

  (Commission
File Number)
 

(IRS Employer

Identification No.)

 

1992 E Silverlake
Tucson AZ, 85713
(Address of principal executive offices, including zip code)

 

Registrant’s telephone number, including area code: (520) 545-1234

 

Not Applicable
(Former name or former address, if changed since last report)

 

Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:

 

Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
   
Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
   
Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
   
Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))

 

Securities registered pursuant to Section 12(b) of the Act:

 

Title of each class   Trading Symbol(s)   Name of each exchange on which registered
Common Stock, par value $0.0001 per share   PMI   The NYSE American, LLC

 

Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).

 

Emerging growth company

 

If an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. 

 

 

 

 

 

 

Item 7.01.Regulation FD Disclosure.

 

On March 25, 2026, Picard Medical, Inc. (the “Company”) held an earnings conference call to discuss the Company’s financial and operating results for the fiscal year ended December 31, 2025. The Company is furnishing as Exhibit 99.1 to this Current Report on Form 8-K the presentation materials that were provided and discussed during the earnings conference call.

 

The information included in Item 7.01, including the exhibit hereto, is being furnished and shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference into any filing of the Company under the Securities Act of 1933, as amended, or the Exchange Act, whether made before or after the date hereof, regardless of any general incorporation language in such filing, except as shall be expressly set forth by specific reference in such filing.

 

Item 9.01. Financial Statements and Exhibits.

 

(d)Exhibits

 

The following exhibits are being furnished herewith:

 

Exhibit No.   Description
99.1   Earnings Conference Call Presentation, dated March 25, 2026
104   Cover Page Interactive Data File (embedded within the Inline XBRL document)

 

1

 

 

SIGNATURE

 

Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.

 

Picard Medical, Inc.  
   
By: /s/ Patrick NJ Schnegelsberg  
  Name: Patrick NJ Schnegelsberg  
  Title: Chief Executive Officer  

 

Dated: March 27, 2026

 

2

 

Exhibit 99.1

 

SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. NYSE: PMI First Annual Business Update March 25, 2026

 

 

This Presentation contains statements that are “forward - looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. Forward - looking statements include all statements that do not relate solely to historical or current facts and can generally be identified by the use of future dates or words such as “may,” “should,” “could,” “will,” “expects,” “seeks to,” “anticipates,” “plans,” “believes,” “estimates,” “intends,” “predicts,” “projects,” “forecast,” “potential” or “continue” or the negative of such terms and other comparable terminology. These statements are not guarantees of future performance and involve risks, uncertainties and assumptions that are difficult to predict. Therefore, actual outcomes and results may differ materially from what is expressed or forecasted in such forward - looking statements due to numerous factors, risks, and uncertainties that could cause actual results to differ materially from such estimates or forecasts. You are cautioned not to unduly rely on such forward - looking statements when evaluating the information in this Presentation. Such forward - looking statements speak only as of the date on which they are made, and the Company does not undertake any obligation to update any forward - looking statement to reflect events or circumstances after the date of this Presentation. Forward - looking statements in this Presentation may include, for example, statements about: the Company's market position, including the belief that SynCardia is a leader in the total artificial heart (“TAH”) market, the Company’s anticipated growth strategy, including expected sales growth and the factors driving such growth, future operations, financial position, estimated revenues and losses, projected capex, prospects and plans; the Company’s strategic advantages and the potential impact those advantages will have on future financial and operational results; the implementation, market acceptance, expected timing of patent and U.S. Food and Drug Administration (“FDA”) approvals, and success of the Company’s products; the Company’s approach and goals with respect to research and development; the Company’s expectations regarding its ability to obtain and maintain intellectual property protection and not infringe on the rights of others; changes in applicable laws or regulations; and the outcome of any known and unknown litigation and regulatory proceedings. Neither the Company nor any of its subsidiaries, affiliates, representatives or advisors assumes any responsibility for or makes any representation or warranty (express or implied) as to the reasonableness, completeness, accuracy or reliability of the estimates and information contained herein, which speak only as of the date identified on the cover page of this Presentation. The Company and its respective affiliates, representatives and advisors expressly disclaim any and all liability based, in whole or in part, on such information, errors therein or omissions therefrom. The forward - looking statements and estimates contained in this Presentation are based on assumptions, expectations, and beliefs as of the date identified on the cover page of this Presentation. Neither the Company nor any of its respective affiliates, representatives or advisors intends to update or otherwise revise the forward - looking statements, estimates and other information contained herein to reflect circumstances existing after the date identified on the cover page of this Presentation or to reflect the occurrence of future events, even if any or all of the underlying assumptions, judgments and estimates are shown to be in error, except as required by law. Additional information about the Company, including risk factors that may affect the Company's business, financial condition, and results of operations, is contained in the Company's filings with the U.S. Securities and Exchange Commission (“SEC”), including the Company's Quarterly Reports on Form 10 - Q, which are available free of charge on the SEC's website at http://www.sec.gov and on the Company's investor relations website at https://picardmedical.com/ . SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Forward - Looking Statements

 

 

General: Picard Medical, Inc. (NYSE American: PMI) (the “Company”) is making this presentation available in connection with an update on its business operations, strategies, and financial results for the year ended December 31, 2025. The information contained in this presentation does not purport to be complete or to contain all of the information that prospective investors or other interested parties may require. This presentation should be read in conjunction with the Company’s filings with the U.S. Securities and Exchange Commission (“SEC”), which are available through the SEC’s EDGAR system at www.sec.gov and on the Company’s website at https://picardmedical.com . Information on the Company’s website or any other website is not incorporated into this presentation by reference. No Offer or Solicitation: This presentation does not constitute an offer to sell or a solicitation of an offer to buy any securities of the Company, nor shall there be any sale of securities in any jurisdiction in which such offer, solicitation, or sale would be unlawful prior to registration or qualification under the securities laws of any such jurisdiction. No securities regulatory authority has expressed an opinion about any securities of the Company and it is an offense to claim otherwise. Guest Speakers: Certain key opinion leaders and patients may participate as guest speakers during this presentation. These individuals have not been compensated by the Company for their participation, and their remarks represent their own independent views, experiences, and opinions. The Company has not provided, reviewed, or approved any written script or prepared remarks for these speakers. The statements made by any guest speaker are their own and do not necessarily reflect the views or positions of Picard Medical, Inc. or any of its affiliates. Nothing stated by a guest speaker should be construed as an endorsement of the Company’s securities or as medical advice. Third - Party Information: Certain information contained in this presentation has been obtained from published and non - published sources prepared by third parties, which in certain cases have not been independently verified. While such information is believed to be reliable, the Company makes no representation or warranty, express or implied, as to the accuracy or completeness of such third - party information, and nothing contained herein is or shall be relied upon as a promise or representation as to the future performance of the Company. Non - GAAP Financial Measures: This presentation may contain financial measures that are not prepared in accordance with U.S. generally accepted accounting principles (“GAAP”). Any non - GAAP financial measures are presented for supplemental informational purposes only and should not be considered a substitute for financial information presented in accordance with GAAP. Reconciliations of any non - GAAP financial measures to the most directly comparable GAAP measures are included in the Company’s filings with the SEC. Trademarks and Copyrights: All trademarks, service marks, and trade names appearing in this presentation are the property of their respective owners. The SynCardia Total Artificial Heart is a product of SynCardia Systems, LLC, a wholly owned subsidiary of Picard Medical, Inc. The contents of this presentation are protected by copyright and may not be reproduced, distributed, or used without the prior written consent of the Company. SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Disclaimers

 

 

Our Mission To pioneer the future of heart replacement by providing the world’s first Total Artificial Heart and developing the next - generation system as an alternative to transplantation ​ SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved.

 

 

Speaker Agenda Item Patrick NJ Schnegelsberg, Chief Executive Officer Welcome, Introductions and Strategic Overview Matt Schuster, Chief Operating Officer Technology and Product Pipeline Matt Schuster, Chief Operating Officer Operational Strategy Bernard Skaggs, Chief Financial Officer Financial Overview Dr. Amy Fiedler, Cardiothoracic Surgeon (KOL) Clinical Experience with SynCardia TAH Marcela P., Former SynCardia Patient Patient Perspective Dr. Zain Khalpey (KOL) Future of Mechanical Circulatory Support Patrick NJ Schnegelsberg, Chief Executive Officer Closing Remarks and Strategic Outlook Management and KOLs Question and Answer Session SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Agenda Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. • Cardiothoracic surgeon specializing in heart transplantation and mechanical circulatory support • Associate Professor of Surgery and Surgical Director Heart Transplantation and Mechanical Circulatory Support, UCSF • Completed surgical training at Massachusetts General Hospital Harvard Medical School • Leads the Heart Transplant and Mechanical Circulatory Support program at UCSF • Surgical Director for Team Heart Rwanda global cardiac surgery initiative • Led the first all - female surgical team to perform a heart transplant in 2022 Dr. Amy Feidler, M.D. Source: Dr. Feidler Disclosure: Dr. Feidler is an independent clinician and has not received compensation from Picard Medical Inc. or SynCardia S yst ems in connection with this presentation.

 

 

SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. • Cardiothoracic surgeon specializing in advanced heart failure and mechanical circulatory support • Chief Medical Artificial Intelligence Officer and Network Director, Artificial Heart Program HonorHealth, Phoenix • M.D., Guy’s, King’s & St Thomas’ School of Medicine, London and PhD. in Cardiothoracic Surgery, Bioenergetics and Cardiac Transplantation Imperial College London • Cardiothoracic surgery training Brigham and Women’s Hospital, Harvard Medical School • Advanced fellowship in mechanical circulatory support and transplantation Columbia University / New York Presbyterian Hospital • Author of 400+ peer reviewed publications and inventor on multiple medical device patents. Dr. Zain Khalpey, MD, PhD, FACS Source: Dr. Khalpey Disclosure: Dr. Khalpey is an independent clinician and has not received compensation from Picard Medical Inc. or SynCardia Systems in connection with this presentation.

 

 

SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. • Diagnosed with Postpartum Cardiomyopathy • Received a SynCardia Total Artificial Heart (STAH) as a bridge to transplant • Spent about 9 months on the device • Successful heart transplant Marcela P. Sources: Marcela P. and SynCardia Systems LLC Disclosure: The patient featured is an individual case and may not be representative of all patient outcomes. The patient has no t received compensation from Picard Medical Inc. or SynCardia Systems. Individual results may vary.

 

 

Opening and Strategic Overview Patrick NJ Schnegelsberg, CEO

 

 

The Problem • ~6.8 million people live with heart failure in the United States • ~56 million globally • ~300,000 patients suffer from advanced heart failure in the United States The Gap • Only ~4,500 heart transplants annually in the United States • Over ~7,000 on the waiting list Our Leadership • SynCardia is the only FDA and Health Canada approved Total Artificial Heart • More than 2,100 implants worldwide SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Advanced Heart Failure: A Major Unmet Need Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC. Donor heart supply remains severely limited Many patients require biventricular circulatory support Established clinical platform and bridge to transplant solution

 

 

Tech Advantage Most mechanical circulatory support technologies treat only one ventricle: • LVADs support the left ventricle • ECMO is temporary support • Temporary devices are short term stabilization tools SynCardia replaces both ventricles and all four heart valves Clinical Validation • First implants performed in the 1980s • First FDA approval in 2004 • Portable Freedom Driver approved in 2014 • Patients supported outside the hospital Future Platform • Development of fully implantable Emperor Total Artificial Heart • Next generation driver technologies • Expanding indications and global markets SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. SynCardia: A Proven Platform with a Path to the Future Purpose Built for Biventricular Support Built on Decades of Clinical Experience Building on the SynCardia Ventricular Platform Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

Clinical Training Clinical Support Centers of Excellence SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. SynCardia Total Artificial Heart Platform Ecosystem Hospital & Home Drivers Driveline Accessories & Services SynCardia TAH Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Key Achievements in 2025 Corporate • Successfully completed initial public offering • $35.55 million total capital raised • Cash burn of $15.67 million (GAAP) Commercial Progress • Revenue increased 12.50% • U.S. represents the majority of Company revenue • Continued expansion of SynCardia adoption at transplant centers Technology Advancement • Continued development of the Emperor fully implantable artificial heart • Progress on next generation driver technologies including Freedom+ and Unicorn Manufacturing and Operations • Initiated transfer of key manufacturing steps including in house valve assembly • Continued technology transfer of external driver manufacturing Global Market Development • Continued progress on regulatory preparation for China NMPA submission • Progress toward expanding access to artificial heart therapy in international markets Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Strategy for Growth in Artificial Heart Therapy Expand Clinical Adaptation Increase implanting centers Strengthen physician training programs Support patient discharge with portable driver technology Regulatory approvals in additional markets Strategic international partnerships Increasing global adoption of artificial heart therapy Expand Global Market Access Advance Next Generation Artificial Heart Technology Fully implantable Emperor Total Artificial Heart Autoregulating electromechanical design Next generation driver technologies Improve Operational Efficiency Manufacturing optimization Expansion of in - house production capabilities Supply chain improvement Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

Technology and Product Pipeline Matt Schuster, COO

 

 

Technology Leadership in Total Artificial Hearts FDA approves Companion C2 Driver FDA approves Freedom Driver FDA approves 50cc STAH US Patents covering fully implantable artificial hearts Patient Hospitalized Patient Mobile in Hospital Patient Mobile in Home Children & Small Adults Alternative to Heart Transplant 2004 2012 2014 2020 2024 FDA approves 70cc STAH First company to receive TAH approval by FDA Next Generation, driver - less STAH; may seek FDA approval in 2028 Notes: Approval years: 2004 – 70cc ventricles; 2012 – Companion C2 driver; 2014 – Freedom Portable Home driver; 2020 – 50cc STAH ventricles. The original CSS driver was used beginning in 2004 until the C2 driver was approved in 2012. Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC. SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved.

 

 

Emperor Total Artificial Heart SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. (1) US Patents: 11,918,798; 12,121,711 & China: CN 115279450 Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC. • Development of a fully implantable artificial heart platform designed to eliminate external pneumatic drivers • Designed to preserve surgical placement and physiologic performance of the current SynCardia system • Incorporates internal power systems, wireless control, and transcutaneous energy transfer • Intended to improve long term patient mobility and quality of life • Three issued U.S. and one issued Chinese patent covering fully implantable artificial heart 1 Goal: Fully Implantable Power and Control Architecture

 

 

• Volume displacement diaphragm pump replacing both ventricles and all four heart valves • Partial fill full eject cycle based on the Frank Starling principle • Automatic adjustment of cardiac output in response to changes in preload and afterload • Physiologic pumping mechanism similar to the native heart Mechanism of Action Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC. SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved.

 

 

• Bench testing demonstrates hemodynamic characteristics consistent with the SynCardia platform • Equivalent stroke volume, cardiac output, and wash characteristics observed • Demonstrates autoregulation in response to changing atrial pressure • Maintains stable output across a range of physiologic conditions Hemodynamic Performance 0 1 2 3 4 5 6 7 4 6 8 10 12 14 Cardiac Output (L/min) Right Atrial Pressure (mmHg) Emperor TAH STAH Emperor Exhibits Frank - Starling Autoregulation Emperor TAH shows increased cardiac output at a constant beat rate in response to increased inflow right atrial pressure, demonstrating autoregulation in response to changing hemodynamics. Testing was conducted at a rate of 125 beats/min SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

• Successfully implanted in multiple porcine models • Animals separated from bypass without complications • Device provided stable circulatory support during observation period • Hemodynamic performance consistent with design objectives Preclinical Feasibility Testing SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Emperor Exhibits Emperor Exhibits in Vivo Autoregulation Emperor TAH shows increased cardiac output at a constant beat rate in response to increased inflow right atrial pressure, demonstrating autoregulation in response to changing hemodynamics. Testing was conducted at a rate of 130 beats/min. Data reflect stable hemodynamic conditions without evidence of suction, atrial collapse, or flow limitation, confirming that the Emperor TAH maintained appropriate preload sensitivity under these operating conditions. Right Atrial Pressure (mmHg) Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

• 2026 – Continued acute animal studies – Design iteration and reliability testing – Potential submission for FDA Breakthrough Device Designation • 2027 – Design freeze – Initiation of GLP animal studies • 2028 – Completion of verification and validation testing – Potential initiation of U.S. clinical study Development Roadmap Emperor Gen 1 Concept SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Sources: Hydrix Ltd, Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Unicorn Driver – Next Generation Portable Artificial Heart System • Next generation portable pneumatic driver system • Intended to reduce size and weight relative to the Freedom driver • Designed to improve battery life, usability, and patient mobility • Potential manufacturing cost advantages through simplified architecture Unicorn Freedom Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

Status Purpose Platform Commercial (FDA) Proven bridge to transplant therapy replacing both ventricles SynCardia Total Artificial Heart Development (Bench) Next generation driver reducing size, weight and cost Unicorn Portable Driver Preclinical (Animals) Fully implantable artificial heart for long term support Emperor Total Artificial Heart SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Artificial Heart Innovation Pipeline Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

Operational Strategy and Manufacturing Initiatives Matt Schuster, COO

 

 

Manufacturing Optimization • Allows U.S. team to focus on implant innovation • Supports lower manufacturing cost • Reduces component obsolescence risk Vertical Integration • Eliminates reliance on external supplier • Improves precision control of valve tolerance • Reduces manufacturing lead time Supply Chain Resilience • Ensures continuity of implant component supply• • Enables supplier cost benchmarking SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Operational Initiatives to Support Scale and Improve Margins Driver Manufacturing Transfer to China Valve Assembly Moved In - House Second Source Qualification Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

Financial Overview Bernard Skaggs, CFO

 

 

• Revenue increased 12.50 percent year over year to $4.94 million • U.S. revenue grew 33.49 percent, representing 88.25 percent of total revenue • Product revenue increased 11.57 percent to $4.75 million and represents 96.07 percent of total revenue Revenue Growth Driven by U.S. Adoption of the SynCardia platform SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC. 0 1 2 3 4 5 6 2024 2025 Revenues by Year and Region ($MM) US Europe Rest of World

 

 

Balance Sheet Cleanup • Repayment of legacy debt and settlement of outstanding accounts payable to stabilize the balance sheet. Transaction and Financing Costs • IPO and financing expenses associated with becoming a public company and securing institutional capital Business Operations and Growth • Operating funds and restricted cash supporting manufacturing, clinical support, and commercialization activities. Deployment of Capital Raised in 2025 SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. • Majority of capital deployed to support ongoing operations and business growth • Legacy liabilities addressed, strengthening the company’s financial foundation • Remaining capital reflects transaction costs associated with the IPO and financing activities 47% 36% 17% Use of Funds (% of $35M Raised) Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

• Approximately $27.00 million net loss • Approximately $14.53 million in non - cash and financing related items(primarily driven by derivative accounting, amortization of debt discount, and other financing related charges) • Approximately $(3.20) million in net working capital changes reflecting timing of accounts payable, inventory, and other operating items • Net cash used in operations (GAAP): (15.67) • Normalized operating cash burn (Non - GAAP): $(11.04) million - 27 14.5 - 3.2 - 11.1 Net Loss Non - cash & … Working capital … Operating Cash … 0 - 5 - 10 - 15 - 20 - 25 - 30 Net Loss to Operating Cash Flow Bridge ($ million) Increase Decrease Total Operating Cash Burn Significantly Lower Than GAAP Net Loss SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

Balance Sheet Strengthened Following Capital Raise and Liability Reduction SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. (1) (1) n/m (not meaningful) because equity moved from negative to positive, so a percentage comparison is not meaningful. (2) Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC. Dec 31 2025 Dec 31 2024 % Change Cash $ 11,451 $ 96 11,828 Inventory $ 7,303 $ 8,115 -10 Other, current $ 1,972 $ 1,580 25 Fixed assets $ 1,822 $ 2,315 -21 Total assets $ 22,548 $ 12,106 86 Accounts payable $ 2,079 $ 5,293 -61 Notes payable $ 6,448 $ 19,976 -68 Derivative liability - $ 6,759 -100 Warrant liability $ 7,842 - n/a Other, current & LT $ 2,390 $ 3,814 -37 Total liabilities $ 18,759 $ 35,842 -48 Temporary equity $ - $ 20,265 n/m (1) Stockholders’ deficit $ 7 $ 1 600 Additional paid-in capital $ 80,397 $ 5,561 1,346 Accumulated other comprehensive income $ 228 $ 278 -18 Accumulated deficit $ (76,843) $ (49,841) -54 Stockholders’ equity (deficit) $ 3,789 $ (44,001) n/m (1) Total liabilities, temporary equity and stockholders’ equity (deficit) $ 22,548 $ 12,106 86 • Additional paid in capital increased significantly following IPO and financing • Stockholders' equity improved from $(44.00)M deficit to $3.78M positive equity

 

 

Total shares outstanding 75,178,535 Warrants 7,710,280 Equity incentive plan 18,000,000 Fully diluted shares 100,888,815 Common shares authorized (1) 150,000,000 Preferred shares authorized 30,000,000 SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Capitalization and Fully Diluted Share Count (1) (1) Figures are as of 3/23/2026. On March 10, 2026 the schareholders voted to increase the number of authorized shares to 30 0 m illion. The Equity Incentive Plan consists only of stock options. The Fullly Diluted Shares includes warrants, options, restri cted and enrestrcted shares. (2) Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Key Financial Priorities for 2026 Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC. Revenue Growth • Expand U.S. implant volumes, the Company’s highest margin market Gross Margin Improvement • Improve gross margins through scale, manufacturing efficiency, and rental program optimization Capital and Cost Management • Strengthen balance sheet through additional capital and disciplined cost management

 

 

Experience with the SynCardia TAH Amy Fiedler, MD Associate Professor of Surgery, Surgical Director of Heart Transplantation and Mechanical Circulatory Support, UCSF

 

 

Amy G. Fiedler, MD Associate Professor of Cardiac Surgery Surgical Director of Heart Transplantation and Mechanical Circulatory Support Total Artificial Heart A Cardiac Surgeons Perspective

 

 

35 Objectives Overview of our heart failure program at UCSF Describe our path to TAH and subsequent growth Review patient selection (key for success) Surgical technique Discuss our institutional outcomes to date Next steps for future growth and collaboration

 

 

36 AHFCCC – UCSF Advanced Heart Failure Comprehensive Care Center ▪ Top 8 heart transplant program in the US ▪ Largest VA ECMO program in the West ▪ 5 th largest LVAD HM3 center in the West

 

 

37 Our journey to TAH It takes a team… ▪ Busy LVAD center ▪ Busy transplant center ▪ Fantastic coordinators + nurses ▪ Innovative leadership ▪ Surgeons with experience

 

 

38 Patient Selection ▪ Biventricular failure ▪ Age ▪ Status of end organs ▪ Multi - disciplinary evaluation ▪ Potential transplant candidacy in the future ▪ Rehabilitation potential

 

 

39 Patient Selection

 

 

40 Surgical Technique – Tips and Tricks ▪ Minimize any unnecessary dissection ▪ Sew the aorta and PA grafts on first ▪ Double layer 3 - 0 MH prolene on sewing cuffs ▪ Loops around SVC, IVC, aorta ▪ Goretex + close pericardium ▪ Delayed chest closure until exquisitely dry

 

 

41 Institutional Outcomes to Date Program began November 2024 ▪ 5 TAH implants - 2 with successful OHT - 1 awaiting discharge - 2 expired

 

 

42 Success Stories

 

 

43 Success Stories

 

 

44 Next Steps for Growth / Collaboration SynCardia x UCSF ▪ UCSF to become a destination center for TAH ▪ Collaborative outreach events across the country promoting TAH x UCSF ▪ Partnering to publish outcomes, best practices, and practice changing techniques ▪ Discuss possibility of cross - collaboration to identify RV failure after LVAD and selecting those patients for TAH support

 

 

45 Thank you!

 

 

Patient Perspective Former SynCardia Patient

 

 

Future of Mechanical Circulatory Support Innovation Zain Khalpey, MD, PhD, FACS Chief Medical Artificial Intelligence Officer, Network Director for the Artificial Heart Program, HonorHealth, Phoenix

 

 

 

 

 

 

 

 

 

 

 

 

 

 

Closing Remarks with Q&A Patrick NJ Schnegelsberg, CEO

 

 

• Continued growth in U.S. adoption, which represents the Company’s highest margin geography • Ongoing development of the next generation technology platforms, including the fully implantable Emperor Total Artificial Heart • Operational initiatives focused on manufacturing efficiency, supply chain resilience, and cost optimization • Continued investment in clinical adoption, physician training, and market expansion • Focus on strengthening the balance sheet and securing additional capital to support operations and technology development • Management remains focused on executing the Company’s long - term strategy to expand access to artificial heart therapy and advance next generation technologies. SynCardia's products are approved for sale in the U.S. and Canada only. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. Key Strategic Priorities for 2026 Sources: Picard Medical Inc SEC filings & SynCardia Systems LLC.

 

 

About SynCardia Systems, LLC SynCardia Systems, LLC, a Picard Medical Company, is headquartered in Tucson, AZ. We manufacture and distribute the world’s f irs t and only US Food and 
 Drug Administration (FDA) and Health Canada approved total artificial heart. The SynCardia Total Artificial Heart is the most widely used and extensively studied artific ial heart in the world. The SynCardia Total Artificial Heart (STAH) The STAH has been successfully implanted in over 2,000 patients suffering from advanced stage heart failure. The implant is a vai lable in two sizes to accommodate patients’ diverse physiologies. The STAH is approved for sale in the US and in Canada where it is indicated for use in cardiac transplant - eligible patients at risk of 
 imminent death from biventricular failure. EU and international approvals are pending. For additional information and label information, visit us at www.syncardia.com. About Heart Failure* Heart failure (HF) is a growing burden for the United States and other developed countries due to the aging of their populati ons . Approximately 6.7 million individuals had HF in 2023 and the prevalence of advanced stage HF has been estimated to be as high as 25% of the total HF populations. Approximately 300,000 (5%) of advanced st age HF are refractory to guideline directed therapy. Medical Advice Disclaimer The information, including but not limited to, text, graphics, images, and other components contained in this material are fo r i nformational purposes only. No 
 information in this material is intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or 
 a qualified health care provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking 
 it because of information you have read in this material. * Bozkurt B, et al., J Card Fail. 2023 Oct;29(10):1412 - 1451; (2) Abouezzeddine et al., Congest Heart Fail. 2011 Jul - Aug;17(4):160 - 8. SynCardia Systems, LLC is a wholly owned subsidiary of Picard Medical Inc. © SynCardia Systems, LLC. All rights reserved. SynCardia's products are approved for sale in the U.S. and Canada only. “Freedom” is a registered trademark of SynCardia Systems, LLC. “ SynCardia Systems”, the SynCardia logo, “Giving the Gift of Time”, “Saving Lives, one Heart at a Time”, “Companion 2 Driver ” are trademarks of SynCardia Systems, LLC. NYSE: PMI

 

FAQ

How did Picard Medical (PMI) perform financially in 2025?

Picard Medical generated 2025 revenue of $4.94 million, up 12.50% year over year. U.S. revenue grew 33.49% and represented 88.25% of total sales. The company still reported an approximate $27.00 million net loss while investing in growth and technology.

What were the key uses of Picard Medical’s 2025 capital raise?

Picard Medical raised $35.55 million in 2025, largely via its IPO. The company deployed funds to repay legacy debt, settle accounts payable, cover IPO and financing costs, and support manufacturing, clinical support, and commercialization activities across its SynCardia artificial heart platform.

How has Picard Medical’s balance sheet changed after the IPO?

Picard Medical’s balance sheet strengthened significantly following its 2025 IPO. Notes payable dropped from $19.976 million to $6.448 million, derivative liabilities were removed, and stockholders’ equity improved from a $(44.001) million deficit to positive $3.789 million as of December 31, 2025.

What is Picard Medical’s main growth driver in the U.S. market?

Growth is driven by increasing U.S. adoption of the SynCardia Total Artificial Heart. In 2025, U.S. revenue rose 33.49% and comprised 88.25% of total revenue, reflecting expanded use at transplant centers and a focus on physician training and patient discharge with portable drivers.

What are Picard Medical’s key technology initiatives like the Emperor Total Artificial Heart?

The Emperor Total Artificial Heart is a fully implantable next-generation system in preclinical development. It aims to eliminate external drivers, using internal power, wireless control, and transcutaneous energy transfer, while Unicorn focuses on a smaller, lighter portable driver to improve mobility and potential cost efficiency.

What are Picard Medical’s financial priorities for 2026?

Picard Medical plans to focus on revenue growth, margin improvement, and capital management. Priorities include expanding high-margin U.S. implant volumes, enhancing manufacturing efficiency and rental programs, and strengthening the balance sheet through additional capital and disciplined cost control to support ongoing technology development.

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