Data / Medical devices / Cradle, Patient, Radiologic / United States
FDA-registered makers of Cradle, Patient, Radiologic in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Cradle, Patient, Radiologic (product code KXH). 2 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
- Cradle, Patient, Radiologic
- Product code
- KXH
- Country
- United States
Makers of Cradle, Patient, Radiologic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| GE Healthcare Coils | Aurora, OH, United States | Specification developer | 1 | November 16, 2012 | 0 | 0 | 0 | api.fda.gov |
| Huestis Machine Corp. | Bristol, RI, United States | Manufacturer | 1 | October 14, 1986 | 0 | 0 | 0 | api.fda.gov |
| Creative Foam Corporation - Bremen | Bremen, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Depuy Orthopaedics, Inc. | Warsaw, IN, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| First Source Inc. | Rochester, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hyperfine, Inc | Guilford, CT, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Orchid Orthopedic Solutions Alabama LLC | Arab, AL, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reina Imaging | Crystal Lake, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| THE INITIATIVE LLC., DBA KyphoLift | South Jordan, UT, United States | Specification developer | 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.