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Picard Medical / SynCardia Releases Annual Stockholder Presentation Ahead of 2026 Annual Meeting

(Moderate)
(Positive)
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Picard Medical (NYSE American: PMI), parent of SynCardia, released a pre-recorded presentation ahead of its July 17, 2026 annual stockholder meeting.

The presentation reviews Q1 revenue up 85% year-over-year, U.S. revenue up 116%, gross margin at 28%, manufacturing optimization, Emperor platform development milestones, and key voting proposals, including director elections and capital structure amendments.

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Positive

  • Revenue increased 85% year-over-year, with gross margin reaching 28% from year-end 2025
  • U.S. revenue grew by 116%, contributing to improved overall financial performance
  • Manufacturing optimization aims to enhance quality control, supply chain resilience, and reduce costs
  • Next-generation Emperor platform advances electromechanical total artificial heart technology
  • Roadmap includes planned FDA Breakthrough Device pursuit, IDE submission in 2028, and clinical activities intent in 2029
  • Annual meeting proposals include capital structure amendments and advisory votes on executive compensation

Negative

  • None.

News Market Reaction – PMI

-1.63%
13 alerts
-1.63% Session close to close
+21.0% Peak in 6 hr 38 min
$20.09M Market Cap
0.2x Rel. Volume

In the Jul 2 session, PMI declined 1.63%, reflecting a mild negative market reaction. Argus tracked a peak move of +21.0% during that session. Our momentum scanner triggered 13 alerts that day, indicating notable trading interest and price volatility.

Data tracked by StockTitan Argus on the day of publication.

Market Context

The presentation underscores rapid growth, with revenue up 85% and gross margin at 28%, alongside a ...
Analysis

The presentation underscores rapid growth, with revenue up 85% and gross margin at 28%, alongside a roadmap to Emperor clinical studies in 2029. Investors may weigh these advances against capital-structure proposals and the company’s ongoing NYSE American compliance work.

Key Figures

Revenue growth: 85% year-over-year increase Gross margin: 28% U.S. revenue growth: 116% increase +4 more
7 metrics
Revenue growth 85% year-over-year increase Recent performance highlighted in annual stockholder presentation
Gross margin 28% Improved from year-end 2025 as noted in presentation
U.S. revenue growth 116% increase Driver of overall revenue and margin improvement
IDE submission timing 2028 Planned Investigational Device Exemption submission for Emperor platform
Planned clinical studies 2029 Intended start of Emperor clinical study activities
Annual meeting date July 17, 2026 Scheduled 2026 Annual Meeting of Stockholders
Meeting time 6:00 p.m. Eastern Time Virtual 2026 Annual Meeting start time

Historical Context

5 past events · Latest: Jun 24 (Neutral)
Pattern 5 events
Date Event Sentiment 24h Move Catalyst
Jun 24 Leadership change Neutral -2.5% CEO stepped down and chairman assumed interim chief executive role.
Jun 16 Conference data plans Positive -3.9% Planned presentation of new in vivo Emperor data and outcome research at ASAIO.
Jun 02 Preclinical study update Positive +60.3% Reported successful acute in vivo implants of next‑generation Emperor total artificial heart.
May 29 Shareholder letter Negative -1.7% Outlined growth but highlighted going‑concern and NYSE American equity compliance issues.
May 21 1Q26 earnings report Negative -8.4% Strong revenue growth but sizable net loss and exchange listing deficiency notices.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Recent news has mostly produced reactions consistent with tone, including a sharp rally on positive Emperor preclinical data and declines around risk- or governance-focused updates.

Key Terms

total artificial heart, breakthrough device designation, investigational device exemption, electromechanical actuation
4 terms
total artificial heart medical
"maker of the world's first total artificial heart approved by both the U.S."
A total artificial heart is a surgically implanted mechanical device that replaces the heart’s two main pumping chambers and takes over circulation, acting like a continuous pump that keeps blood moving through the body. Investors care because it is a high-cost, high-stakes medical product whose commercial success depends on clinical trial results, regulatory approvals, hospital adoption, reimbursement rules and long-term patient outcomes — factors that drive revenue potential and risk.
breakthrough device designation regulatory
"milestones for this initial configuration include pursuit of FDA Breakthrough Device designation"
A breakthrough device designation is a regulatory program that gives promising medical devices for serious or life‑threatening conditions priority support and faster review from a health authority (e.g., the U.S. FDA). Think of it as a “fast lane” or VIP pass through development and review: it can shorten time to market, lower regulatory uncertainty, and boost a company’s commercial prospects — but it is not an approval by itself.
investigational device exemption regulatory
"a planned Investigational Device Exemption submission in 2028"
An investigational device exemption (IDE) is a regulatory permission that allows a medical device maker to test an unapproved device in people so the device’s safety and effectiveness can be studied. For investors, an IDE matters because it marks a formal step toward regulatory approval—like getting a temporary test-drive permit—and influences clinical cost, timelines, and the likelihood a device will reach the market and generate revenue.
electromechanical actuation technical
"a new electromechanical actuation platform designed to eliminate the external pneumatic driver"
A system that converts electrical signals into physical motion to move or control parts—using motors, solenoids or similar components—so a device can push, pull, rotate or position something without human hands. Think of it like the small motor in a remote-control toy that turns the wheels. For investors, electromechanical actuation matters because it drives product performance, energy use, reliability and manufacturing cost, all of which affect revenue potential and long-term competitiveness.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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- Presentation Highlights Business Progress, Product Development Milestones, and Matters for Stockholder Consideration-

TUCSON, Ariz., July 02, 2026 (GLOBE NEWSWIRE) -- Picard Medical, Inc. (NYSE American: PMI) ("Picard Medical" or the "Company"), parent company of SynCardia Systems, LLC ("SynCardia"), maker of the world's first total artificial heart approved by both the U.S. Food and Drug Administration and Health Canada, today announced the availability of its pre-recorded presentation in advance of the Company's 2026 Annual Meeting of Stockholders, scheduled for July 17, 2026. The presentation provides stockholders with an overview of the Company's recent business performance, product development progress, manufacturing initiatives, and the proposals to be considered at the Annual Meeting.

"Despite recent leadership changes, our mission remains unchanged," said Richard Fang, Ph.D., Interim Chief Executive Officer and Chairman of the Board. "We remain committed to advancing the development of a fully implantable total artificial heart while continuing to support physicians and patients with our current technologies. Our presentation highlights the meaningful progress we have made across our business, from strong first-quarter financial performance to continued innovation in our next-generation Emperor platform, and provides stockholders with important information regarding the proposals to be voted on at the Annual Meeting."

Among the business updates highlighted in the presentation were steady financial milestones including an 85% year-over-year increase in revenue and improved gross margin of 28% from year-end 2025, driven by a 116% increase of U.S. revenue Picard Medical also discussed ongoing manufacturing optimization initiatives designed to strengthen quality control, improve supply chain resilience, and reduce production costs.

The presentation also provides an update on the Company's next-generation Emperor platform, which builds on the clinically proven SynCardia Total Artificial Heart architecture through the Emperor Drive System, a new electromechanical actuation platform designed to eliminate the external pneumatic driver used with the Company's current products. The Company's initial Emperor configuration retains an external controller and battery, with a longer-term roadmap toward a fully implantable system utilizing wireless power transfer and internal control. Development milestones for this initial configuration include pursuit of FDA Breakthrough Device designation, continued preclinical studies, a planned Investigational Device Exemption submission in 2028, and an intent to begin clinical study activities in 2029, the scope and design of which will be determined in consultation with FDA.

The presentation concludes with an overview of the proposals to be considered by stockholders at the 2026 Annual Meeting, including the election of directors, proposed amendments to the Company's capital structure, ratification of its independent registered public accounting firm, and advisory votes regarding executive compensation. Stockholders are encouraged to review the Company's proxy materials and submit their votes prior to the meeting.

The Company's 2026 Annual Meeting of Stockholders will be held virtually on Friday, July 17, 2026, at 6:00 p.m. Eastern Time. Stockholders of record as of the applicable record date are eligible to vote by internet, telephone, or during the virtual meeting.

About Picard Medical and SynCardia

Picard Medical, Inc. is the parent company of SynCardia Systems, LLC (“SynCardia”), the Tucson, Arizona–based leader with the only commercially available total artificial heart technology for patients with end-stage heart failure. SynCardia develops, manufactures, and commercializes the SynCardia Total Artificial Heart (“STAH”), an implantable system that assumes the full functions of a failing or failed human heart. It is the first artificial heart approved by both the FDA and Health Canada, and it remains the only commercially available artificial heart in the United States and Canada. With more than 2,100 implants performed at hospitals across 27 countries, the STAH is the most widely used and extensively studied artificial heart in the world. For additional information about Picard Medical, please visit www.picardmedical.com or review the Company’s filings with the U.S. Securities and Exchange Commission (the “SEC”) at www.sec.gov.

Forward-looking Statements

This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that are based on management’s current expectations, assumptions, and beliefs and involve risks and uncertainties. Forward-looking statements are statements that are not historical facts. Forward-looking statements can often be identified by words such as “anticipate,” “believe,” “continue,” “expect,” “goal,” “intend,” “may,” “plan,” “remain,” “target,” “will,” “advance,” “expand,” and similar expressions, and variations or negatives of these words.

These statements include, but are not limited to, statements regarding the Company’s financial condition, future operating results, commercialization activities, expectations for growth, expanding utilization of the SynCardia Total Artificial Heart, expanding patient access at transplant centers, supporting clinical partners, advancing development of the Emperor Total Artificial Heart and other next-generation technologies, regulatory submissions and approvals, manufacturing and supply chain initiatives, capital raising activities, strengthening the Company’s commercial and financial position, strategic initiatives, leadership transitions, and other statements that are not historical facts.

Such forward-looking statements are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied by the forward-looking statements. Factors that may cause such differences include, but are not limited to, risks relating to the Company’s ability to obtain additional financing, maintain compliance with applicable stock exchange listing requirements, achieve commercial adoption of its products, obtain regulatory approvals, execute manufacturing and supply chain initiatives, successfully develop next-generation technologies, manage market conditions, and other risks described in the Company’s filings with the U.S. Securities and Exchange Commission (”SEC”).

The Company expressly disclaims any obligation or undertaking to publicly update or revise any forward-looking statements contained herein, whether as a result of new information, future events, changed circumstances, or otherwise, 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 SEC, including the Company’s Annual Report on Form 10-K and Quarterly Reports on Form 10-Q, which are available free of charge at www.sec.gov and on the Company’s investor relations website at www.picardmedical.com.

Contact:

Investors
Eric Ribner
Managing Director
LifeSci Advisors LLC
eric@lifesciadvisors.com

Picard Medical, Inc./SynCardia Systems, LLC
IR@picardmedical.com

General/Media
Brittany Lanza
blanza@syncardia.com


FAQ

What did Picard Medical (NYSE American: PMI) announce in its 2026 annual stockholder presentation?

Picard Medical released a pre-recorded 2026 annual stockholder presentation covering financial performance, product development, manufacturing, and voting proposals. According to Picard Medical, it highlights Q1 revenue growth, margin improvements, Emperor platform milestones, and key agenda items for the July 17, 2026 virtual annual meeting.

How did Picard Medical (PMI) describe its recent financial performance in the 2026 stockholder presentation?

Picard Medical reported an 85% year-over-year revenue increase and a 28% gross margin from year-end 2025. According to Picard Medical, U.S. revenue rose 116%, demonstrating steady financial milestones alongside ongoing efforts to optimize manufacturing, quality control, and supply chain resilience across its SynCardia artificial heart business.

What is Picard Medical’s Emperor platform mentioned in the July 2026 presentation for PMI shareholders?

The Emperor platform is Picard Medical’s next-generation system building on the SynCardia Total Artificial Heart. According to Picard Medical, its Emperor Drive System replaces the external pneumatic driver with electromechanical actuation, initially retaining an external controller and battery, with a roadmap toward a fully implantable, wirelessly powered configuration.

What clinical and regulatory milestones did Picard Medical outline for the Emperor platform for PMI?

Picard Medical plans to pursue FDA Breakthrough Device designation and continue preclinical studies for Emperor. According to Picard Medical, it targets an Investigational Device Exemption submission in 2028 and intends to begin clinical study activities in 2029, with scope and design determined in consultation with FDA.

What proposals will Picard Medical (PMI) stockholders vote on at the 2026 annual meeting?

Stockholders will vote on electing directors, capital structure amendments, auditor ratification, and advisory executive compensation items. According to Picard Medical, the presentation summarizes these proposals and encourages stockholders to review proxy materials and vote by internet, telephone, or during the virtual July 17, 2026 meeting.

When is the 2026 Picard Medical (PMI) annual stockholder meeting and who can vote?

Picard Medical’s 2026 annual stockholder meeting will be held virtually on July 17, 2026, at 6:00 p.m. Eastern Time. According to Picard Medical, stockholders of record as of the applicable record date may vote online, by phone, or at the virtual meeting.

How is Picard Medical improving manufacturing for SynCardia products according to its 2026 presentation?

Picard Medical is pursuing manufacturing optimization initiatives for its SynCardia artificial heart products. According to Picard Medical, these efforts aim to strengthen quality control, improve supply chain resilience, and reduce production costs, supporting both current external-driver systems and future Emperor platform configurations in development.