Bioserenity Medical Devices Group is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Bioserenity Medical Devices Group - FDA 510(k) Cleared Devices
Recent clearances: IceCap product line
1
Total
1
Cleared
0
Denied
Bioserenity Medical Devices Group has 1 FDA 510(k) cleared medical devices. Based in Paris, FR.
Latest FDA clearance: Mar 2025. Active since 2025. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Bioserenity Medical Devices Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Bioserenity Medical Devices Group
1 devices