Data / Medical devices / Absorbable Synthetic Wound Dressing / United States
FDA-registered makers of Absorbable Synthetic Wound Dressing in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Absorbable Synthetic Wound Dressing (product code QSZ). 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
- Absorbable Synthetic Wound Dressing
- Product code
- QSZ
- Country
- United States
Makers of Absorbable Synthetic Wound Dressing in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Anika Therapeutics, Inc. | Bedford, MA, United States | Complaint file establishment, Manufacturer | 2 | September 2, 2026 | 0 | 0 | 0 | api.fda.gov |
| Acera Surgical, Inc. C/O Linda Braddon, PhD | Woodstock, GA, United States | Complaint file establishment, Specification developer | 2 | September 25, 2020 | 0 | 0 | 0 | api.fda.gov |
| Acera Surgical - Adie Road | Maryland Heights, MO, United States | Manufacturer | 1 | May 18, 2023 | 0 | 0 | 0 | api.fda.gov |
| Ets Wound Care LLC | Rolla, MO, United States | Manufacturer | 1 | September 15, 2016 | 0 | 0 | 0 | api.fda.gov |
| Nanofiber Solutions LLC | Dublin, OH, United States | Manufacturer | 1 | March 2, 2018 | 0 | 0 | 0 | api.fda.gov |
| SiOxMed, LLC | Winston Salem, NC, United States | Complaint file establishment, Manufacturer | 1 | July 5, 2024 | 0 | 0 | 0 | api.fda.gov |
| Poly-Med, Inc. | Piedmont, SC, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Quality Tech Services, LLC | Bloomington, MN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Surgical Technologies, Inc. | St. Paul, MN, 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.