Data / Medical devices / Radiological Image Processing Software For Radiation Therapy
Radiological Image Processing Software For Radiation Therapy (QKB): 20 FDA-registered makers in 9 countries
20 establishments in 9 countries are registered with the FDA to make Radiological Image Processing Software For Radiation Therapy (product code QKB, Class 2, 21 CFR 892.2050). 16 of them have a 510(k) clearance or PMA approval on file and 0 have a recall event. The FDA has issued 49 510(k) clearances under this code, the latest on August 14, 2026, and lists 0 recall events (0 Class I). FDA data exported November 2, 2026.
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- Product code
- QKB
- Device class
- 2
- Regulation
- 892.2050
- Medical specialty
- Radiology
Makers by country
| Country | Makers |
|---|---|
| United States | 8 |
| China | 3 |
| Germany | 2 |
| South Korea | 2 |
| Taiwan | 1 |
| France | 1 |
| Finland | 1 |
| Hungary | 1 |
| Canada | 1 |
Makers of Radiological Image Processing Software For Radiation Therapy
Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.
| 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 |
| Siemens Healthineers AG | ERLANGEN Bavaria, Germany | Manufacturer | 5 | April 10, 2026 | 0 | 0 | 0 | api.fda.gov |
| Manteia Technologies Co.,ltd. | Xiamen Fujian, China | Manufacturer | 4 | January 23, 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 |
| EverFortune.AI Co., Ltd. | Taichung City, Taiwan | Manufacturer | 3 | January 28, 2026 | 0 | 0 | 0 | api.fda.gov |
| Therapanacea | Paris, France | Manufacturer | 3 | April 19, 2023 | 0 | 0 | 0 | api.fda.gov |
| MVISION AI Oy | Helsinki Uusimaa, Finland | Manufacturer | 2 | October 18, 2024 | 0 | 0 | 0 | api.fda.gov |
| Oncosoft Inc. | Seoul, South Korea | Complaint file establishment, Exporter to the US, Manufacturer | 2 | July 2, 2026 | 0 | 0 | 0 | api.fda.gov |
| Coreline Soft Co., Ltd. | Seoul, South Korea | Manufacturer | 1 | November 10, 2022 | 0 | 0 | 0 | api.fda.gov |
| Ge Healthcare | Chicago, IL, United States | Manufacturer | 1 | April 1, 2025 | 0 | 0 | 0 | api.fda.gov |
| GE Healthcare Magyarorszag Kft. | Budapest, Hungary | Specification developer | 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 |
| Limbus Ai | Toronto Ontario, Canada | Complaint file establishment, Manufacturer | 1 | October 9, 2024 | 0 | 0 | 0 | api.fda.gov |
| Medmind Technology Co., Ltd. | Beijing, China | Manufacturer | 1 | December 15, 2021 | 0 | 0 | 0 | api.fda.gov |
| Siemens Healthineers AG Varian Cancer Therapy (CTH) | Erlangen Bavaria, Germany | Manufacturer | 1 | July 10, 2026 | 0 | 0 | 0 | api.fda.gov |
| Wisdom Technologies, Inc. | Hefei Anhui, China | Manufacturer | 1 | May 7, 2024 | 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 August 14, 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.