Data / Medical devices / Radiological Image Processing Software For Radiation Therapy / United States
FDA-registered makers of Radiological Image Processing Software For Radiation Therapy in the United States: 8 establishments
8 establishments in the United States are registered with the FDA to make Radiological Image Processing Software For Radiation Therapy (product code QKB). 4 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
- Radiological Image Processing Software For Radiation Therapy
- Product code
- QKB
- Country
- United States
Makers of Radiological Image Processing Software For Radiation Therapy in the United States
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Mim Software Inc. | Cleveland, OH, United States | Complaint file establishment, Manufacturer | 7 | March 27, 2026 | 0 | 0 | 0 | api.fda.gov |
| Radformation, Inc. | New York, NY, United States | Manufacturer | 4 | August 14, 2026 | 0 | 0 | 0 | api.fda.gov |
| Ge Healthcare | Chicago, IL, United States | Manufacturer | 1 | April 1, 2025 | 0 | 0 | 0 | api.fda.gov |
| Ge Medical Systems, LLC | Waukesha, WI, United States | Manufacturer, Specification developer | 1 | May 4, 2023 | 0 | 0 | 0 | api.fda.gov |
| Carina Medical LLC | Ashburn, VA, United States | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ge Medical Systems, LLC | Waukesha, WI, United States | Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| GEXPRO, a Division of REXEL USA, Inc. | Menomonee Falls, WI, United States | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Neosoma, Inc. | Groton, MA, 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.