Data / Medical devices / Bed, Patient Rotation, Powered / United States
FDA-registered makers of Bed, Patient Rotation, Powered in the United States: 11 establishments
11 establishments in the United States are registered with the FDA to make Bed, Patient Rotation, Powered (product code IKZ). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 3, 2026.
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- Device
- Bed, Patient Rotation, Powered
- Product code
- IKZ
- Country
- United States
Makers of Bed, Patient Rotation, Powered in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Agiliti Health - Corona | Corona, CA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Agiliti Health - Ellis | Ellis, KS, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Agiliti Health - Hays | Hays, KS, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Encompass Group, LLC. | McDonough, GA, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kap Medical | Corona, CA, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Kreg Medical, Inc. | Melrose Park, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Larand LLC | Naperville, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Seneca Devices Inc | Durham, NC, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Stryker Medical | Portage, MI, United States | Complaint file establishment, Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| The Side Lyer Company | Orlando, FL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Turn Medical, LLC | San Antonio, TX, United States | Complaint file establishment, 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.