Data / Medical devices / Mesh, Surgical, Collagen, Large Abdominal Wall Defects / United States
FDA-registered makers of Mesh, Surgical, Collagen, Large Abdominal Wall Defects in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Mesh, Surgical, Collagen, Large Abdominal Wall Defects (product code OXK). 2 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
- Mesh, Surgical, Collagen, Large Abdominal Wall Defects
- Product code
- OXK
- Country
- United States
Makers of Mesh, Surgical, Collagen, Large Abdominal Wall Defects in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Lifecell Corp | Branchburg, NJ, United States | Manufacturer | 1 | April 17, 2013 | 0 | 0 | 0 | api.fda.gov |
| Lifecell Corp. | Branchburg, NJ, United States | Complaint file establishment, Manufacturer | 1 | April 17, 2013 | 0 | 0 | 0 | api.fda.gov |
| Acell, Inc. | Columbia, MD, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Colorado Therapeutics LLC | Louisville, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cook Biotech, Inc. | West Lafayette, IN, 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.