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SeaStar Medical to Present at Upcoming Investor Summit Conference

Key Takeaway: SeaStar Medical will present at the Virtual Investor Summit Conference on June 24, 2026. CEO Eric Schlorff will discuss the company's focus on treatments for critically ill patients facing organ failure. SeaStar's QUELIMMUNE® product is FDA approved for life-threatening Acute Kidney Injury in pediatric patients, and the company is conducting pivotal trials for adult patients.

Market Sentiment Analysis

POSITIVE FACTORS

  • CEO Eric Schlorff will present at a significant investor conference.
  • SeaStar Medical's product QUELIMMUNE® is FDA approved for a rare condition.
  • The company has received Breakthrough Device Designation for multiple indications.
  • Ongoing pivotal clinical trials aim to address critical health issues.

Full Press Release Details

DENVER, June 22, 2026 (GLOBE NEWSWIRE) -- SeaStar Medical Holding Corporation (Nasdaq: ICU), a commercial-stage healthcare company focused on transformational treatments for critically ill patients facing organ failure and potential loss of life, announced today that Eric Schlorff, Chief Executive Officer of SeaStar Medical, will present at the Virtual Investor Summit Conference on Wednesday, June 24that 10:30 am Eastern Time.
Interested investors can register and view the live presentation here:SeaStar Medical Events / Presentations
A replay of the SeaStar Medical presentation will be available on the Company's website and can be accessedhere. The replay will be available for up to 30 days following its posting.

About SeaStar Medical

SeaStar Medical is a commercial-stage healthcare company focused on transformational treatments for critically ill patients facing organ failure and potential loss of life. SeaStar Medical’s first commercial product,QUELIMMUNE®(SCD-PED), was approved in 2024 by the U.S. Food and Drug Administration (FDA). It is the only FDA approved product for the ultra-rare condition of life-threatening Acute Kidney Injury (AKI) due to sepsis or a septic condition requiring renal replacement therapy (RRT) in critically ill pediatric patients. SeaStar Medical’s Selective Cytopheretic Device (SCD) therapy has been awarded Breakthrough Device Designation for six therapeutic indications by the FDA, enabling the potential for a speedier pathway to approval and preferable reimbursement dynamics at commercial launch. The company is currently conducting the NEUTRALIZE-AKI pivotal clinical trial of its SCD therapy in adult patients with AKI requiring continuous renal replacement therapy, a life-threatening condition with no effective treatment options that impacts over 200,000 adults in the U.S. annually.
For more information visitwww.seastarmedical.comor visit us onLinkedInorX.

Contact:SeaStar Investor Relations:IR@SeaStarMed.com

Frequently Asked Questions

When is SeaStar Medical's presentation at the Investor Summit?

The presentation is scheduled for June 24, 2026, at 10:30 am Eastern Time.

What is SeaStar Medical's focus?

The company focuses on transformational treatments for critically ill patients facing organ failure.

What is QUELIMMUNE®?

QUELIMMUNE® is SeaStar Medical's FDA-approved product for life-threatening Acute Kidney Injury.

What designation has SeaStar Medical received from the FDA?

The company has received Breakthrough Device Designation for six therapeutic indications.

What trial is SeaStar Medical currently conducting?

They are conducting the NEUTRALIZE-AKI pivotal clinical trial for adult patients with AKI.

Last updated: Jun 22, 2026