Data / Medical devices / Intervertebral Fusion Device With Integrated Fixation, Cervical / Germany
FDA-registered makers of Intervertebral Fusion Device With Integrated Fixation, Cervical in Germany: 12 establishments
12 establishments in Germany are registered with the FDA to make Intervertebral Fusion Device With Integrated Fixation, Cervical (product code OVE). 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
- Intervertebral Fusion Device With Integrated Fixation, Cervical
- Product code
- OVE
- Country
- Germany
Makers of Intervertebral Fusion Device With Integrated Fixation, Cervical in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Silony Medical GMBH | Leinfelden-Echterdingen Baden-Wurttemberg, Germany | Complaint file establishment, Specification developer | 5 | June 24, 2015 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Sofamor Danek Deggendorf GMBH | DEGGENDORF Bavaria, Germany | Manufacturer | 4 | January 21, 2015 | 0 | 0 | 0 | api.fda.gov |
| Aesculap AG | TUTTLINGEN, DONAU Baden-Wurttemberg, Germany | Manufacturer | 1 | May 25, 2016 | 0 | 0 | 0 | api.fda.gov |
| Signus Medizintechnik GMBH | ALZENAU Bavaria, Germany | Complaint file establishment, Exporter to the US, Manufacturer, Specification developer | 1 | February 11, 2025 | 0 | 0 | 0 | api.fda.gov |
| Christian Diener GMBH | TUTTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eurofins STERIPAC GMBH | Calw-Altburg Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Friedrich Daniels GMBH | SOLINGEN North Rhine-Westphalia, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Hipp Medical AG | Renquishausen Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Jabil Tuttlingen Manufacturing GmbH | Tuttlingen Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Procon Medizintechnik GMBH | Alzenau Bavaria, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Ptumedical GMBH | Spaichingen Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| ProCon Implants GmbH | Tuttlingen 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.