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UC Davis Health Among First in Nation to Evaluate the Supira pVAD System in SUPPORT II Study

SACRAMENTO, Calif., June 26, 2026 – UC Davis Health has launched enrollment for the SUPPORT II Pivotal Study, evaluating the investigational Supira System. This low-profile percutaneous ventricular assist device (pVAD) is designed to provide critical, temporary hemodynamic support for high-risk patients undergoing complex coronary stenting procedures.

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UC Davis Health Among First in Nation to Evaluate the Supira pVAD System in SUPPORT II Study2026-06-29T14:08:08-07:00

CentraCare Heart & Vascular First in Midwest to Enroll Patient in SUPPORT II Study

ST. CLOUD, Minn. – June 23, 2026 - CentraCare Heart & Vascular recently shared a major clinical milestone on LinkedIn, announcing their program as the first in the Midwest to successfully enroll a patient in the SUPPORT II clinical trial evaluating the investigational Supira System.

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CentraCare Heart & Vascular First in Midwest to Enroll Patient in SUPPORT II Study2026-08-18T15:55:22-07:00

Supira Medical Announces FDA Approval for SUPPORT II Pivotal Trial, Advances in Cardiogenic Shock, and Appointment of D. Keith Grossman to Board of Directors

LOS GATOS, Calif., April 8, 2026 – Supira Medical, Inc. (Supira), a clinical-stage company focused on transforming the percutaneous ventricular assist device (pVAD) market, today announced FDA approval to initiate the SUPPORT II Pivotal Trial. The trial is designed to support a future PMA submission and represents a critical step toward U.S. market entry.

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Supira Medical Announces FDA Approval for SUPPORT II Pivotal Trial, Advances in Cardiogenic Shock, and Appointment of D. Keith Grossman to Board of Directors2026-06-29T13:53:26-07:00

Supira Medical Secures $120M Oversubscribed Series E Financing and Completes Enrollment of SUPPORT I Early Feasibility Study in the United States

LOS GATOS, CA., March 26, 2025 – Supira Medical, Inc. (Supira), a clinical-stage Shifamed portfolio company, today announced the successful completion of an oversubscribed Series E financing round, raising $120M to accelerate the company’s mission of transforming the percutaneous ventricular assist device (pVAD) market.

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Supira Medical Secures $120M Oversubscribed Series E Financing and Completes Enrollment of SUPPORT I Early Feasibility Study in the United States2026-06-29T13:53:58-07:00

Supira Medical Initiates U.S. Early Feasibility Study (EFS) for High-Risk PCI

LOS GATOS, Calif., Nov. 21, 2024 – Supira Medical, Inc. (Supira), a Shifamed portfolio company, announced today the initiation and successful patient enrollment in the company’s U.S. EFS. This multi-center prospective, single arm clinical study will evaluate the safety and feasibility of Supira’s innovative low-profile, high-flow percutaneous ventricular assist device (pVAD) in patients undergoing high-risk percutaneous coronary intervention (HRPCI).

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Supira Medical Initiates U.S. Early Feasibility Study (EFS) for High-Risk PCI2026-06-29T13:54:30-07:00
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