Data / Medical devices / Peripheral Blood Processing Device For Wound Management / United States
FDA-registered makers of Peripheral Blood Processing Device For Wound Management in the United States: 5 establishments
5 establishments in the United States are registered with the FDA to make Peripheral Blood Processing Device For Wound Management (product code PMQ). 0 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
- Peripheral Blood Processing Device For Wound Management
- Product code
- PMQ
- Country
- United States
Makers of Peripheral Blood Processing Device For Wound Management in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Innovate Medical, LLC | Johnson City, TN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Millstone Medical Outsourcing LLC. | Fall River, MA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Mimix Awc | Tampa, FL, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Royal Biologics, Inc. | Hackensack, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Regenlab USA LLC | Jersey City, NJ, United States | 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.