Data / Medical devices / United States / Okapi Medical Dba Resivant Medical
Okapi Medical Dba Resivant Medical: FDA-registered device maker in Akron, OH, United States, 1 510(k) clearance
Okapi Medical Dba Resivant Medical is registered with the FDA (registration 3031294900) in Akron, OH, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 20, 2024. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3031294900
- Address
- 526 S Main St # 124m, Akron, OH, United States, 44311
- Owner or operator
- Okapi Medical dba Resivant Medical (10092381)
- Roles
- Manufacturer
- First device listed
- December 30, 2024
- Registered through
- 2026
- Brand names listed
- CUTIVA(TM) PLUS Skin Closure System (RM-1739)
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Cutaneous Tissue Adhesive With Mesh | OMD | 2 | Manufacturer | accessdata.fda.gov |
| Tissue Adhesive For The Topical Approximation Of Skin | MPN | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 20, 2024 | K234114 | CUTIVA(TM) Topical Skin Adhesive (RM-1700); CUTIVA(TM) PLUS Skin Closure System (RM-1739) | MPN | Substantially Equivalent | Okapi Medical, LLC Dba Resivant Medical | accessdata.fda.gov |
Compare with other makers
- All makers of Tissue Adhesive For The Topical Approximation Of Skin
- All makers of Cutaneous Tissue Adhesive With Mesh
Updated August 20, 2024. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.