Okapi Medical, LLC Dba Resivant Medical is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Okapi Medical, LLC Dba Resivant Medical - FDA 510(k) Cleared Devices
Recent clearances: CUTIVA™ Topical Skin Adhesive (RM1700), CUTIVA(TM) Topical Skin Adhesive (RM-1700)
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