Data / Medical devices / United States / Progressive Wound Care Technologies, LLC
Progressive Wound Care Technologies, LLC: FDA-registered device maker in Savannah, GA, United States, 1 510(k) clearance
Progressive Wound Care Technologies, LLC is registered with the FDA (registration 3008562678) in Savannah, GA, United States. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated March 12, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3008562678
- Address
- 1212 E Montgomery Cross Road, Unit B, Savannah, GA, United States, 31406
- Owner or operator
- Progressive Wound Care Technologies, LLC (10033392)
- Roles
- Manufacturer, Repackager or relabeler, Specification developer
- First device listed
- August 11, 2010
- Registered through
- 2026
- Brand names listed
- GelTex® White Foam Dressing, IodoFoam®, Ioplex®, LipoGel®
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Dressing, Wound, Drug | FRO | U | Manufacturer, Repackager or relabeler, Specification developer | accessdata.fda.gov |
| Dressing, Wound, Hydrogel Without Drug And/Or Biologic | NAE | 1 | Manufacturer, Repackager or relabeler | accessdata.fda.gov |
| Dressing, Wound, Hydrophilic | NAC | 1 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| March 12, 2013 | K122634 | IODOFOAM IODOPHOR FOAM DRESSING | FRO | Substantially Equivalent | Progressive Wound Care Technologies, LLC | accessdata.fda.gov |
Compare with other makers
- All makers of Dressing, Wound, Hydrogel Without Drug And/Or Biologic
- All makers of Dressing, Wound, Hydrophilic
- All makers of Dressing, Wound, Drug
Updated March 12, 2013. 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.