Data / Medical devices / Barrier, Control Panel, X-Ray, Movable / United States
FDA-registered makers of Barrier, Control Panel, X-Ray, Movable in the United States: 9 establishments
9 establishments in the United States are registered with the FDA to make Barrier, Control Panel, X-Ray, Movable (product code IWX). 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
- Barrier, Control Panel, X-Ray, Movable
- Product code
- IWX
- Country
- United States
Makers of Barrier, Control Panel, X-Ray, Movable in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Aadco Medical, Inc. | Randolph, VT, United States | Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Cardio Medical Products, Inc. | Rockaway, NJ, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Image Diagnostics, Inc. | Fitchburg, MA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Intech Partners LLC | Oak Ridge North, TX, United States | Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Phillips Safety Products, Inc. | Middlesex, NJ, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Protech Leaded Eyewear, Inc. | West Palm Beach, FL, United States | Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Techno-Aide, Inc. | Whites Creek, TN, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Weslacova | North Wilkesboro, NC, United States | Contract manufacturer | 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 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.