Data / Medical devices / Holder, Head, Radiographic / United States
FDA-registered makers of Holder, Head, Radiographic in the United States: 13 establishments
13 establishments in the United States are registered with the FDA to make Holder, Head, Radiographic (product code IWY). 0 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
- Holder, Head, Radiographic
- Product code
- IWY
- Country
- United States
Makers of Holder, Head, Radiographic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Anholt Technologies Inc. | Avondale, PA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Cassemco, Inc. | Cookeville, TN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Creative Foam Corporation - Bremen | Bremen, IN, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Dental Imaging Technologies Corporation | Quakertown, PA, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Domico Med-Device, LLC | Fenton, MI, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hyperfine, Inc | Guilford, CT, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Klarity Medical Products, LLC | Heath, OH, United States | Contract manufacturer, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medtec LLC | Orange City, IA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neocis Inc | Miami, FL, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Radiation Products Design, Inc. | Albertville, MN, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Standard Imaging, Inc. | Middleton, WI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Techno-Aide, Inc. | Whites Creek, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Xoran Technologies, LLC | Ann Arbor, MI, United States | 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.