Data / Medical devices / Mesh, Surgical, Absorbable, Staple Line Reinforcement / United States
FDA-registered makers of Mesh, Surgical, Absorbable, Staple Line Reinforcement in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Mesh, Surgical, Absorbable, Staple Line Reinforcement (product code OXC). 5 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 2, 2026.
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- Device
- Mesh, Surgical, Absorbable, Staple Line Reinforcement
- Product code
- OXC
- Country
- United States
Makers of Mesh, Surgical, Absorbable, Staple Line Reinforcement in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ethicon Endo-Surgery, LLC | Guaynabo, PR, United States | Specification developer | 3 | January 9, 2026 | 0 | 0 | 0 | api.fda.gov |
| Ethicon Endo-Surgery, Inc. | Cincinnati, OH, United States | Specification developer | 2 | January 9, 2026 | 0 | 0 | 0 | api.fda.gov |
| Teleflex LLC (NADC) | Olive Branch, MS, United States | Manufacturer | 1 | October 6, 2023 | 0 | 0 | 0 | api.fda.gov |
| Teleflex Medical Inc. | Cincinnati, OH, United States | Specification developer | 1 | October 6, 2023 | 0 | 0 | 0 | api.fda.gov |
| W. L. Gore & Associates, Inc. | Elkton, MD, United States | Manufacturer | 1 | August 17, 2018 | 0 | 0 | 0 | api.fda.gov |
| Bard Shannon Limited | Humacao, PR, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Covidien | North Haven, CT, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Davol Inc., Sub. C.R. Bard, Inc. | Warwick, RI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtronic Distribution Center | Memphis, TN, United States | Manufacturer | 0 | 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.