Data / Medical devices / Tissue Adhesive For The Topical Approximation Of Skin / United States
FDA-registered makers of Tissue Adhesive For The Topical Approximation Of Skin in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Tissue Adhesive For The Topical Approximation Of Skin (product code MPN). 9 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Tissue Adhesive For The Topical Approximation Of Skin
- Product code
- MPN
- Country
- United States
Makers of Tissue Adhesive For The Topical Approximation Of Skin in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| H.B. Fuller Medical Adhesive Technologies, LLC | Hudson, NC, United States | Manufacturer, Repackager or relabeler, Specification developer | 6 | May 13, 2014 | 0 | 0 | 0 | api.fda.gov |
| Chemence Medical Inc. | Alpharetta, GA, United States | Complaint file establishment, Manufacturer, Manufacturer for export | 5 | September 9, 2021 | 0 | 0 | 0 | api.fda.gov |
| Covidien | North Haven, CT, United States | Repackager or relabeler, Specification developer | 2 | October 26, 2015 | 1 | 0 | 0 | api.fda.gov |
| Ethicon, Inc. | Somerville, NJ, United States | Manufacturer | 1 | October 22, 2015 | 0 | 1 | 0 | api.fda.gov |
| Ethicon, Inc. | Raritan, NJ, United States | Specification developer | 1 | October 22, 2015 | 0 | 0 | 0 | api.fda.gov |
| Ethicon, LLC. | San Lorenzo, PR, United States | Manufacturer | 1 | October 22, 2015 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Distribution Center | Memphis, TN, United States | Manufacturer | 1 | October 26, 2015 | 0 | 0 | 0 | api.fda.gov |
| Okapi Medical Dba Resivant Medical | Akron, OH, United States | Manufacturer | 1 | August 20, 2024 | 0 | 0 | 0 | api.fda.gov |
| OptMed, Inc | New York, NY, United States | Complaint file establishment, Specification developer | 1 | September 19, 2025 | 0 | 0 | 0 | api.fda.gov |
Updated November 2, 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.