Author: Serenity Medical

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

June 30, 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)

March 31, 2026

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