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

Serenity Medical, a NeuroTechnology Investors (NTI) portfolio company and pioneer in venous sinus stenosis treatment, today announced the Company received U.S. Food and Drug Administration (FDA) ...
Reuters

Candela gets FDA OK for pain-reducing device

Aug 28 (Reuters) - Candela Corp. said it received an additional clearance from the U.S. Food and Drug Administration for its Serenity device, used to reduce pain during all laser and intense pulse ...