Data / Medical devices / Device, Patient Transfer, Powered / United States
FDA-registered makers of Device, Patient Transfer, Powered in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Device, Patient Transfer, Powered (product code FRZ). 1 has a 510(k) clearance or PMA approval on file and 2 have a recall event. FDA data exported November 3, 2026.
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- Device
- Device, Patient Transfer, Powered
- Product code
- FRZ
- Country
- United States
Makers of Device, Patient Transfer, Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Diacor, Inc. | Mount Pleasant, UT, United States | Manufacturer | 1 | January 17, 2013 | 0 | 0 | 0 | api.fda.gov |
| Agiliti Health - Corona | Corona, CA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Anholt Technologies Inc. | Avondale, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cardinal Health | Riverview, FL, United States | Manufacturer, Reprocessor | 0 | 0 | 0 | 0 | api.fda.gov | |
| D.T. Davis Enterprises Ltd. | Allentown, PA, United States | Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Design Specific Us Inc | Wilmington, DE, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hatch Product Development LLC | Wauconda, IL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medline ReNewal | Redmond, OR, United States | Reprocessor | 0 | 0 | 0 | 0 | api.fda.gov | |
| Patient Positioning Systems, LLC | Annapolis, MD, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Prism Pacific Industries LLC | Sacramento, CA, United States | Complaint file establishment, Repackager or relabeler, Reprocessor | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Sustainability Solutions | Tempe, AZ, United States | Specification developer | 0 | 0 | 1 | 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.