Medical Device Manufacturer · US , Akron , OH

Okapi Medical, LLC Dba Resivant Medical - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2024
2
Total
2
Cleared
0
Denied

Okapi Medical, LLC Dba Resivant Medical has 2 FDA 510(k) cleared medical devices. Based in Akron, US.

Latest FDA clearance: Aug 2025. Active since 2024. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Okapi Medical, LLC Dba Resivant Medical Filter by specialty or product code using the sidebar.

FDA 510(k) cleared devices by Okapi Medical, LLC Dba Resivant Medical

2 devices
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