Data / Medical devices / Marker, Radiographic, Implantable / Germany
FDA-registered makers of Marker, Radiographic, Implantable in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Marker, Radiographic, Implantable (product code NEU). 2 have a 510(k) clearance or PMA approval on file and 0 have a recall event. FDA data exported November 3, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- Device
- Marker, Radiographic, Implantable
- Product code
- NEU
- Country
- Germany
Makers of Marker, Radiographic, Implantable in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| SOMATEX Medical Technologies GmbH | Berlin, Germany | Complaint file establishment, Specification developer | 4 | February 18, 2021 | 0 | 0 | 0 | api.fda.gov |
| Surgmark GMBH | Auerbach i. d. Oberpfalz Bavaria, Germany | Manufacturer | 1 | January 23, 2024 | 0 | 0 | 0 | api.fda.gov |
| Alpo Medizintechnik GMBH | Auerbach in der Oberpfalz Bavaria, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Alleima Karlsruhe GmbH | Karlsruhe Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| PROMOTEC-MEDIZINTECHNIK GmbH | Blankenfelde / Mahlow Brandenburg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov |
Updated November 3, 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.