Data / Medical devices / System, X-Ray, Angiographic / Germany
FDA-registered makers of System, X-Ray, Angiographic in Germany: 9 establishments
9 establishments in Germany are registered with the FDA to make System, X-Ray, Angiographic (product code IZI). 6 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
- System, X-Ray, Angiographic
- Product code
- IZI
- Country
- Germany
Makers of System, X-Ray, Angiographic in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Siemens Healthineers AG | FORCHHEIM Bavaria, Germany | Exporter to the US, Manufacturer | 7 | May 3, 2018 | 0 | 0 | 0 | api.fda.gov |
| Carl Zeiss Meditec AG (oberkochen) | OBERKOCHEN Baden-Wurttemberg, Germany | Manufacturer | 3 | June 20, 2023 | 0 | 0 | 0 | api.fda.gov |
| Surgvision GMBH | Muenchen Bavaria, Germany | Manufacturer, Specification developer | 3 | March 20, 2024 | 0 | 0 | 0 | api.fda.gov |
| Aesculap AG | TUTTLINGEN, DONAU Baden-Wurttemberg, Germany | Complaint file establishment, Manufacturer | 1 | January 21, 2021 | 0 | 0 | 0 | api.fda.gov |
| Diagnostic Green GMBH | Munich Bavaria, Germany | Specification developer | 1 | September 22, 2025 | 0 | 0 | 0 | api.fda.gov |
| Xiralite GMBH | Berlin, Germany | Manufacturer | 1 | January 31, 2014 | 0 | 0 | 0 | api.fda.gov |
| Askion GMBH | Gera Thuringia, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Intuitive Surgical Optics GmbH | Freiburg Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Schoelly Fiberoptic, GMBH | DENZLINGEN Baden-Wurttemberg, Germany | 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.