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) Regulatory Record - Okapi Medical, LLC Dba Resivant Medical
2 devices
1-2 of 2
Filters