Data / Medical devices / System, Planning, Radiation Therapy Treatment / Germany
FDA-registered makers of System, Planning, Radiation Therapy Treatment in Germany: 8 establishments
8 establishments in Germany are registered with the FDA to make System, Planning, Radiation Therapy Treatment (product code MUJ). 6 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
- System, Planning, Radiation Therapy Treatment
- Product code
- MUJ
- Country
- Germany
Makers of System, Planning, Radiation Therapy Treatment in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Siemens Healthineers AG | FORCHHEIM Bavaria, Germany | Manufacturer | 7 | April 26, 2024 | 0 | 0 | 0 | api.fda.gov |
| Brainlab Se | Munich Bavaria, Germany | Exporter to the US, Manufacturer | 6 | October 5, 2026 | 0 | 5 | 0 | api.fda.gov |
| Siemens Healthineers AG Varian Cancer Therapy (CTH) | Erlangen Bavaria, Germany | Complaint file establishment, Manufacturer, Specification developer | 5 | March 18, 2026 | 0 | 0 | 0 | api.fda.gov |
| Varian Medical Systems Haan GmbH | Haan North Rhine-Westphalia, Germany | Manufacturer | 4 | October 23, 2024 | 0 | 0 | 0 | api.fda.gov |
| Bebig Medical GMBH | Berlin, Germany | Manufacturer | 1 | May 20, 2015 | 0 | 0 | 0 | api.fda.gov |
| Medcom GMBH | Darmstadt Hesse, Germany | Manufacturer | 1 | March 27, 2018 | 0 | 0 | 0 | api.fda.gov |
| Siemens Healthineers AG | ERLANGEN Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Varian Medical Systems Haan GmbH Manufacturing site Kemnath | Kemnath Bavaria, Germany | 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.