Data / Medical devices / Film, Radiographic / United States
FDA-registered makers of Film, Radiographic in the United States: 17 establishments
17 establishments in the United States are registered with the FDA to make Film, Radiographic (product code IWZ). 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
- Film, Radiographic
- Product code
- IWZ
- Country
- United States
Makers of Film, Radiographic in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Air Techniques, Inc. | Melville, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Aktina Medical Corp. | Congers, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ashland | Columbus, OH, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ashland Specialty Ingredients, G.P. | Bridgewater, NJ, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Aspen Surgical Products, Inc. | Caledonia, MI, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ashland Specialty Ingredients, G.P. | Fiskeville, RI, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Bioseal | Placentia, CA, United States | Contract manufacturer, Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Codonics, Inc. | Middleburg Heights, OH, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carestream Dental LLC | Atlanta, GA, United States | Complaint file establishment, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carestream Health, Inc | Rochester, NY, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carestream Health, Inc. | White City, OR, United States | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Carestream Health, Inc. | Rochester, NY, United States | Manufacturer, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| HPC Medx | Hanover, PA, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ortho Organizers, Inc. | Savannah, GA, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Sun Nuclear Corporation | Norfolk, VA, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| White Mountain Imaging | Concord, NH, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Wolf X-Ray Corp | Battleboro, NC, United States | Manufacturer, Repackager or relabeler | 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.