Data / Medical devices / Cutaneous Tissue Adhesive With Mesh / United States
FDA-registered makers of Cutaneous Tissue Adhesive With Mesh in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Cutaneous Tissue Adhesive With Mesh (product code OMD). 4 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
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- Device
- Cutaneous Tissue Adhesive With Mesh
- Product code
- OMD
- Country
- United States
Makers of Cutaneous Tissue Adhesive With Mesh in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ethicon, Inc. | Somerville, NJ, United States | Manufacturer | 3 | December 7, 2021 | 0 | 0 | 0 | api.fda.gov |
| Ethicon, Inc. | Raritan, NJ, United States | Specification developer | 3 | December 7, 2021 | 0 | 0 | 0 | api.fda.gov |
| Ethicon, LLC. | San Lorenzo, PR, United States | Manufacturer | 3 | December 7, 2021 | 0 | 0 | 0 | api.fda.gov |
| Chemence Medical Inc. | Alpharetta, GA, United States | Manufacturer | 2 | June 5, 2020 | 0 | 0 | 0 | api.fda.gov |
| Okapi Medical Dba Resivant Medical | Akron, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 2026. 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.