Hyprevention - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Hyprevention has 1 FDA 510(k) cleared medical devices. Based in Pessac, FR.
Latest FDA clearance: Feb 2024. Active since 2024. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Hyprevention Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hyprevention, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Hyprevention
1 devices