Data / Medical devices / Dressing, Wound And Burn, Occlusive
Dressing, Wound And Burn, Occlusive (MGP): 11 FDA-registered makers in 4 countries
11 establishments in 4 countries are registered with the FDA to make Dressing, Wound And Burn, Occlusive (product code MGP, Class U). 7 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 80 510(k) clearances under this code, the latest on October 25, 2001, and lists 1 recall event (0 Class I). FDA data exported November 2, 2026.
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- Product code
- MGP
- Device class
- U
- Medical specialty
- Unknown
Makers by country
| Country | Makers |
|---|---|
| United States | 8 |
| Canada | 1 |
| China | 1 |
| Mexico | 1 |
Makers of Dressing, Wound And Burn, Occlusive
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| 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 |
| Derma Sciences Canada, Inc | TORONTO Ontario, Canada | Manufacturer | 1 | November 2, 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 | |
| Derma Sciences Nantong Incorporation | DEVELOPMENT Jiangsu, China | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Teleflex Medical de Mexico, S. de R.L. de C.V. | NUEVO LAREDO Tamaulipas, Mexico | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated October 25, 2001. 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.