Keri Medical SA - FDA 510(k) Cleared Devices
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) cleared devices by Keri Medical SA
1 devices