Medical Device Manufacturer · CH , Geneva

Keri Medical SA - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2022
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.

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