Data / Medical devices / Exerciser, Powered / Germany
FDA-registered makers of Exerciser, Powered in Germany: 10 establishments
10 establishments in Germany are registered with the FDA to make Exerciser, Powered (product code BXB). 0 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
- Exerciser, Powered
- Product code
- BXB
- Country
- Germany
Makers of Exerciser, Powered in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| BTT Health GMBH | Greifenberg Bavaria, Germany | Manufacturer, Specification developer | 0 | 0 | 1 | 0 | api.fda.gov | |
| DJO Global / Germany | Freiburg Baden-Wurttemberg, Germany | Exporter to the US, Manufacturer, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| H/P/Cosmos Sports & Medical GMBH | NUSSDORF BEI TRAUNSTEIN Bavaria, Germany | Contract manufacturer, Exporter to the US, Manufacturer, Remanufacturer, Repackager or relabeler, Specification developer | 0 | 0 | 0 | 0 | api.fda.gov | |
| JK Products GMBH | BAD HONNEF North Rhine-Westphalia, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| KBL GmbH | Dernbach Rhineland-Palatinate, Germany | Complaint file establishment, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Medica Medizintechnik GMBH | HOCHDORF Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDIREHA GmbH | Umkirch Baden-Wurttemberg, Germany | Contract manufacturer, Exporter to the US | 0 | 0 | 0 | 0 | api.fda.gov | |
| Novotec Medical GMBH | PFORZHEIM Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reck-Technik GMBH & Co. KG | BETZENWEILER Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Reha-Stim Medtec GMBH | Berlin, Germany | 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.