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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

CountryMakers
United States8
China3
Germany2
South Korea2
Taiwan1
France1
Finland1
Hungary1
Canada1

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.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Mim Software Inc.Cleveland, OH, United StatesComplaint file establishment, Manufacturer7March 27, 2026000api.fda.gov
Siemens Healthineers AGERLANGEN Bavaria, GermanyManufacturer5April 10, 2026000api.fda.gov
Manteia Technologies Co.,ltd.Xiamen Fujian, ChinaManufacturer4January 23, 2026000api.fda.gov
Radformation, Inc.New York, NY, United StatesManufacturer4August 14, 2026000api.fda.gov
EverFortune.AI Co., Ltd.Taichung City, TaiwanManufacturer3January 28, 2026000api.fda.gov
TherapanaceaParis, FranceManufacturer3April 19, 2023000api.fda.gov
MVISION AI OyHelsinki Uusimaa, FinlandManufacturer2October 18, 2024000api.fda.gov
Oncosoft Inc.Seoul, South KoreaComplaint file establishment, Exporter to the US, Manufacturer2July 2, 2026000api.fda.gov
Coreline Soft Co., Ltd.Seoul, South KoreaManufacturer1November 10, 2022000api.fda.gov
Ge HealthcareChicago, IL, United StatesManufacturer1April 1, 2025000api.fda.gov
GE Healthcare Magyarorszag Kft.Budapest, HungarySpecification developer1April 1, 2025000api.fda.gov
Ge Medical Systems, LLCWaukesha, WI, United StatesManufacturer, Specification developer1May 4, 2023000api.fda.gov
Limbus AiToronto Ontario, CanadaComplaint file establishment, Manufacturer1October 9, 2024000api.fda.gov
Medmind Technology Co., Ltd.Beijing, ChinaManufacturer1December 15, 2021000api.fda.gov
Siemens Healthineers AG Varian Cancer Therapy (CTH)Erlangen Bavaria, GermanyManufacturer1July 10, 2026000api.fda.gov
Wisdom Technologies, Inc.Hefei Anhui, ChinaManufacturer1May 7, 2024000api.fda.gov
Carina Medical LLCAshburn, VA, United StatesManufacturer0000api.fda.gov
Ge Medical Systems, LLCWaukesha, WI, United StatesSpecification developer0000api.fda.gov
GEXPRO, a Division of REXEL USA, Inc.Menomonee Falls, WI, United StatesContract manufacturer0000api.fda.gov
Neosoma, Inc.Groton, MA, United StatesManufacturer0000api.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.