Data / Medical devices / Holder, Head, Neurosurgical (Skull Clamp) / Germany
FDA-registered makers of Holder, Head, Neurosurgical (Skull Clamp) in Germany: 8 establishments
8 establishments in Germany are registered with the FDA to make Holder, Head, Neurosurgical (Skull Clamp) (product code HBL). 3 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
- Holder, Head, Neurosurgical (Skull Clamp)
- Product code
- HBL
- Country
- Germany
Makers of Holder, Head, Neurosurgical (Skull Clamp) in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Black Forest Medical GmbH | FREIBURG Baden-Wurttemberg, Germany | Manufacturer | 8 | April 24, 2024 | 0 | 3 | 1 | api.fda.gov |
| Brainlab Se | Munich Bavaria, Germany | Manufacturer | 1 | April 26, 2013 | 0 | 0 | 0 | api.fda.gov |
| Medical Bees GMBH | Emmingen-Liptingen Baden-Wurttemberg, Germany | Manufacturer | 1 | November 6, 2025 | 0 | 0 | 0 | api.fda.gov |
| Eurofins Inpac Medizintechnik GMBH | Birkenfeld Baden-Wurttemberg, Germany | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eurofins Inpac Medizintechnik GMBH | Birkenfeld Baden-Wurttemberg, Germany | Contract manufacturer, Contract sterilizer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Eurofins STERIPAC GMBH | Calw-Altburg Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| NORAS MRI products GMBH | HOECHBERG Bavaria, Germany | Contract manufacturer, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Siemens Healthineers AG | ERLANGEN Bavaria, Germany | Specification developer | 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.