Hyprevention Sas is one of 174 FDA 510(k) medical device manufacturers from France in the dataset, ranked by real submission volume.
Hyprevention Sas - FDA 510(k) Cleared Devices
Recent clearances: V-STRUT Vertebral Implant
1
Total
1
Cleared
0
Denied
Hyprevention Sas has 1 FDA 510(k) cleared medical devices. Based in Pessac Cedex, FR.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Hyprevention Sas 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 Sas
1 devices