Data / Medical devices / Oral Wound Dressing / United States
FDA-registered makers of Oral Wound Dressing in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Oral Wound Dressing (product code OLR). 8 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
- Oral Wound Dressing
- Product code
- OLR
- Country
- United States
Makers of Oral Wound Dressing in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Forward Science Technologies LLC | Houston, TX, United States | Manufacturer | 2 | December 22, 2022 | 0 | 0 | 0 | api.fda.gov |
| MPM Medical | Mesquite, TX, United States | Specification developer | 2 | May 10, 2006 | 0 | 0 | 0 | api.fda.gov |
| 3-D Matrix, Inc. | Newton, MA, United States | Complaint file establishment, Manufacturer | 1 | October 8, 2021 | 0 | 0 | 0 | api.fda.gov |
| DenTek Oral Care, Inc. | Tarrytown, NY, United States | Complaint file establishment, Specification developer | 1 | September 18, 2019 | 0 | 0 | 0 | api.fda.gov |
| Inter-Med, Inc. | Racine, WI, United States | Manufacturer | 1 | May 27, 2020 | 0 | 0 | 0 | api.fda.gov |
| Soleva Pharma LLC | Robbinsville, NJ, United States | Complaint file establishment, Manufacturer, Specification developer | 1 | December 11, 2006 | 0 | 0 | 0 | api.fda.gov |
| Tricol Biomedical, INC. | Portland, OR, United States | Specification developer | 1 | July 7, 2006 | 0 | 0 | 0 | api.fda.gov |
| Unicare Biomedical, Inc. | Laguna Hills, CA, United States | Repackager or relabeler, Specification developer | 1 | July 24, 2009 | 0 | 0 | 0 | api.fda.gov |
| Accupac, LLC | Mainland, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Acupac Packaging, Inc. | Mahwah, NJ, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Innovize | North Oaks, MN, United States | Contract 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.