Data / Medical devices / System, X-Ray, Mobile / United States
FDA-registered makers of System, X-Ray, Mobile in the United States: 15 establishments
15 establishments in the United States are registered with the FDA to make System, X-Ray, Mobile (product code IZL). 14 have a 510(k) clearance or PMA approval on file and 4 have a recall event. FDA data exported November 2, 2026.
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- Device
- System, X-Ray, Mobile
- Product code
- IZL
- Country
- United States
Makers of System, X-Ray, Mobile in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Ge Medical Systems, LLC | Waukesha, WI, United States | Manufacturer, Specification developer | 6 | April 28, 2021 | 0 | 12 | 0 | api.fda.gov |
| Minxray, Inc. | Northbrook, IL, United States | Manufacturer | 5 | March 19, 2021 | 0 | 0 | 0 | api.fda.gov |
| Source-Ray, Inc. | Ronkonkoma, NY, United States | Manufacturer | 5 | December 12, 2016 | 0 | 0 | 0 | api.fda.gov |
| Aspen Imaging Healthcare, Inc | Plano, TX, United States | Complaint file establishment, Manufacturer | 2 | May 28, 2025 | 0 | 0 | 0 | api.fda.gov |
| Carestream Health, Inc | Rochester, NY, United States | Manufacturer, Specification developer | 2 | March 11, 2026 | 0 | 3 | 0 | api.fda.gov |
| First Source Inc. | Rochester, NY, United States | Manufacturer, Specification developer | 2 | July 3, 2024 | 0 | 1 | 0 | api.fda.gov |
| Livermoretech,inc | Plano, TX, United States | Complaint file establishment, Manufacturer | 2 | May 28, 2025 | 0 | 0 | 0 | api.fda.gov |
| Repair Operations Center | Oak Creek, WI, United States | Remanufacturer | 2 | April 28, 2021 | 0 | 0 | 0 | api.fda.gov |
| Del Medical, Inc. | Bloomingdale, IL, United States | Manufacturer | 1 | November 20, 2017 | 0 | 1 | 0 | api.fda.gov |
| Kub Technologies, Inc. | Stratford, CT, United States | Manufacturer | 1 | October 29, 2014 | 0 | 0 | 0 | api.fda.gov |
| Oxos Medical, Inc | Atlanta, GA, United States | Complaint file establishment, Manufacturer, Remanufacturer, Repackager or relabeler | 1 | February 4, 2022 | 0 | 0 | 0 | api.fda.gov |
| Remote Technologies, Inc. | Port Chester, NY, United States | Manufacturer | 1 | September 6, 1991 | 0 | 0 | 0 | api.fda.gov |
| RadmediX, LLC | Dayton, OH, United States | Manufacturer | 1 | April 13, 2020 | 0 | 0 | 0 | api.fda.gov |
| X-Cel X-Ray Corp. | Crystal Lake, IL, United States | Manufacturer | 1 | August 9, 1993 | 0 | 0 | 0 | api.fda.gov |
| Uih Technologies, LLC | Houston, TX, United States | Contract 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.