Data / Medical devices / Holder, Radiographic Cassette, Wall-Mounted / United States
FDA-registered makers of Holder, Radiographic Cassette, Wall-Mounted in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Holder, Radiographic Cassette, Wall-Mounted (product code IXY). 0 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.
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- Device
- Holder, Radiographic Cassette, Wall-Mounted
- Product code
- IXY
- Country
- United States
Makers of Holder, Radiographic Cassette, Wall-Mounted in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aktina Medical Corp. | Congers, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Accogent Pausch | Eatontown, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Core Labs, LLC. | Englewood, CO, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Del Medical, Inc. | Bloomingdale, IL, United States | Manufacturer, Repackager or relabeler | 0 | 0 | 1 | 0 | api.fda.gov | |
| Livermoretech,inc | Plano, TX, United States | Manufacturer, Remanufacturer, Repackager or relabeler | 0 | 0 | 0 | 0 | api.fda.gov | |
| Marketlab Incorporated | Caledonia, MI, United States | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| RCI Operating CO LLC | Hilton, NY, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reina Imaging | Crystal Lake, IL, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Summit Industries, LLC | Niles, IL, 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.