Data / Medical devices / Stimulator, Muscle, Powered / Germany
FDA-registered makers of Stimulator, Muscle, Powered in Germany: 6 establishments
6 establishments in Germany are registered with the FDA to make Stimulator, Muscle, Powered (product code IPF). 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
- Stimulator, Muscle, Powered
- Product code
- IPF
- Country
- Germany
Makers of Stimulator, Muscle, Powered in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Gbo Medizintechnik AG | Rimbach Hesse, Germany | Manufacturer | 2 | June 2, 2026 | 0 | 0 | 0 | api.fda.gov |
| Healy GMBH | Kraenzlin Brandenburg, Germany | Manufacturer | 1 | December 14, 2021 | 0 | 0 | 0 | api.fda.gov |
| Pajunk GMBH Medizintechnologie | GEISINGEN Baden-Wurttemberg, Germany | Complaint file establishment, Manufacturer | 1 | November 24, 2023 | 0 | 0 | 0 | api.fda.gov |
| TimeWaver Production GMBH | Kraenzlin Brandenburg, Germany | Manufacturer | 1 | December 14, 2021 | 0 | 0 | 0 | api.fda.gov |
| Zimmer Medizinsysteme GMBH | NEU-ULM Bavaria, Germany | Manufacturer | 1 | February 19, 2021 | 0 | 0 | 0 | api.fda.gov |
| Miha Bodytec GMBH | Gersthofen Bavaria, 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.