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) ...
UCSF Radiology

Imaging Pulsatile Tinnitus with 4D Flow MRI

Patients with pulsatile tinnitus are beset by a sound that surges with every beat of their heart. For those who seek medical ...
Forbes

Breakthrough Treatment Shows Promise In Curing Chronic Headaches And Tinnitus

Forbes contributors publish independent expert analyses and insights. An experienced weaver of health, technology, ethics and spirituality. Adel Gitman spent two years plagued by tinnitus. “Imagine ...
Morningstar

Sonorous Neurovascular Receives FDA Breakthrough Device Designation for BosSTENT™, First Braided Self-Expanding Cerebral Venous Stent, to Treat Debilitating Pulsatile Tinnitus

LAKE FOREST, Calif., Feb. 5, 2026 /PRNewswire/ -- Sonorous Neurovascular, a pioneering medical device company dedicated to advancing neurovascular therapies, today announced that the U.S. Food and ...
Medscape

How Should I Manage the Patient With Tinnitus?

Patients with asymmetric hearing loss and/or unilateral tinnitus should always have additional testing with an otolaryngology specialist. Patients with pulsatile tinnitus must have specialty care and ...
manilatimes

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

Second FDA Regulatory Milestone for Serenity’s Novel Platform, Following the Recent HDE Approval of the River Stent™ - First Venous Stent for Severe, Refractory Idiopathic Intracranial Hypertension ...
Mena FN

Serenity Medical Receives U.S. FDA Breakthrough Device Designation For The Serenity Shepherd Stenttm System To Treat Pulsatile Tinnitus

(MENAFN- GlobeNewsWire - Nasdaq) Second FDA Regulatory Milestone for Serenity's Novel Platform, Following the Recent HDE Approval of the River StentTM – First Venous Stent for Severe, Refractory ...