Keri Medical SA is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Keri Medical SA - FDA 510(k) Cleared Devices
Recent clearances: KeriFlex® MCP and PIP Finger Joint Prostheses
1
Total
1
Cleared
0
Denied
Keri Medical SA has 1 FDA 510(k) cleared medical devices. Based in Geneva, CH.
Last cleared in 2022. Active since 2022. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Keri Medical SA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Keri Medical SA
1 devices