Data / Medical devices / Filler, Bone Void, Calcium Compound / Germany
FDA-registered makers of Filler, Bone Void, Calcium Compound in Germany: 9 establishments
9 establishments in Germany are registered with the FDA to make Filler, Bone Void, Calcium Compound (product code MQV). 5 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
- Filler, Bone Void, Calcium Compound
- Product code
- MQV
- Country
- Germany
Makers of Filler, Bone Void, Calcium Compound in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Curasan AG | KLEINOSTHEIM Bavaria, Germany | Specification developer | 3 | September 17, 2018 | 0 | 0 | 0 | api.fda.gov |
| Curasan AG, Frankfurt Facility | FRANKFURT Hesse, Germany | Manufacturer | 3 | September 17, 2018 | 0 | 0 | 0 | api.fda.gov |
| Medtronic Sofamor Danek Deggendorf GMBH | DEGGENDORF Bavaria, Germany | Manufacturer | 3 | April 19, 2013 | 0 | 0 | 0 | api.fda.gov |
| Biocomposites GmbH (former ARTOSS GmbH) | Rostock Mecklenburg-Western Pomerania, Germany | Manufacturer | 2 | April 7, 2025 | 0 | 0 | 0 | api.fda.gov |
| Signus Medizintechnik GMBH | ALZENAU Bavaria, Germany | Complaint file establishment, Exporter to the US, Manufacturer, Specification developer | 1 | September 28, 2009 | 0 | 0 | 0 | api.fda.gov |
| BBF Sterilisationsservice GMBH | Kernen 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 | |
| Friedrich Daniels GMBH | SOLINGEN North Rhine-Westphalia, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MedSkin Solutions Dr. Suwelack AG | BILLERBECK North Rhine-Westphalia, 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.