Serenity Medical Receives U.S. FDA Breakthrough Device Designation for The Serenity Shepherd Stent™ System to Treat Pulsatile Tinnitus
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June 30, 2026

Serenity Medical Receives U.S. FDA Breakthrough Device Designation for The Serenity Shepherd Stent™ System to Treat Pulsatile Tinnitus

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March 31, 2026

Serenity Medical Receives U.S. FDA HDE Approval of the River™ Stent – the First Venous Stent Approved for Severe, Refractory Idiopathic Intracranial Hypertension (IIH)

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