Medical Device Manufacturer · CH , Burgdorf

Genostis AF - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
1
Total
1
Cleared
0
Denied

Genostis AF has 1 FDA 510(k) cleared medical devices. Based in Burgdorf, CH.

Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Genostis AF Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Genostis AF

1 devices
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