Data / Medical devices / Dressing, Wound And Burn, Occlusive / United States
FDA-registered makers of Dressing, Wound And Burn, Occlusive in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Dressing, Wound And Burn, Occlusive (product code MGP). 6 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
- Dressing, Wound And Burn, Occlusive
- Product code
- MGP
- Country
- United States
Makers of Dressing, Wound And Burn, Occlusive in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Carwild Corp. | New London, CT, United States | Contract manufacturer, Manufacturer | 1 | October 21, 1997 | 0 | 0 | 0 | api.fda.gov |
| Conmed Corporation | Utica, NY, United States | Complaint file establishment, Manufacturer | 1 | March 24, 1995 | 0 | 0 | 0 | api.fda.gov |
| Conmed Corporation | Westborough, MA, United States | Specification developer | 1 | March 24, 1995 | 0 | 0 | 0 | api.fda.gov |
| Signa Medical, Inc. | Long Beach, NY, United States | Repackager or relabeler, Specification developer | 1 | November 12, 1997 | 0 | 0 | 0 | api.fda.gov |
| Teleflex LLC (NADC) | Olive Branch, MS, United States | Manufacturer, Repackager or relabeler | 1 | August 1, 1994 | 0 | 0 | 0 | api.fda.gov |
| Teleflex Medical LLC | Morrisville, NC, United States | Complaint file establishment, Specification developer | 1 | August 1, 1994 | 0 | 0 | 0 | api.fda.gov |
| C.G. Laboratories-Bob White | Granbury, TX, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| CG Converting And Packaging, LLC | Granbury, TX, United States | Contract 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.