Okapi Medical Dba Resivant Medical
Country not established FDA establishment FEI 3031294900
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
CUTIVA(TM) Topical Skin Adhesive (RM-1700); CUTIVA(TM) PLUS Skin Closure System (RM-1739) Ref K234114
510(k) 510(k)- 510(k) 510(k)
Company details
- FDA FEI number
- 3031294900
- Address
- 526 S Main St # 124m, Akron, OH, 44311
Frequently asked questions
How many devices does OKAPI MEDICAL DBA RESIVANT MEDICAL have in the registry?
The registry currently lists 2 devices for OKAPI MEDICAL DBA RESIVANT MEDICAL. Devices recorded under merged duplicate company entries are counted once.
Which registries list OKAPI MEDICAL DBA RESIVANT MEDICAL's devices?
Among its 2 most recently registered devices, OKAPI MEDICAL DBA RESIVANT MEDICAL has devices listed in FDA 510(k) (2 devices).
What risk classes do OKAPI MEDICAL DBA RESIVANT MEDICAL's devices fall under?
Among its 2 most recently registered devices, the classes recorded for OKAPI MEDICAL DBA RESIVANT MEDICAL's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from OKAPI MEDICAL DBA RESIVANT MEDICAL in the registry?
The most recently registered devices listed for OKAPI MEDICAL DBA RESIVANT MEDICAL include CUTIVA(TM) Topical Skin Adhesive (RM-1700); CUTIVA(TM) PLUS Skin Closure System (RM-1739) and CUTIVA™ Topical Skin Adhesive (RM1700); CUTIVA™ PLUS Skin Closure System (RM1739).