Data / Medical devices / Massager, Therapeutic, Electric / Germany
FDA-registered makers of Massager, Therapeutic, Electric in Germany: 10 establishments
10 establishments in Germany are registered with the FDA to make Massager, Therapeutic, Electric (product code ISA). 1 has 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
- Massager, Therapeutic, Electric
- Product code
- ISA
- Country
- Germany
Makers of Massager, Therapeutic, Electric in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| MTS Medical AG | KONSTANZ Baden-Wurttemberg, Germany | Manufacturer | 2 | October 12, 2022 | 0 | 0 | 0 | api.fda.gov |
| Gbo Medizintechnik AG | Rimbach Hesse, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| JK Products GMBH | BAD HONNEF North Rhine-Westphalia, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Likamed GMBH | Eppingen Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| MEDIREHA GmbH | Umkirch Baden-Wurttemberg, Germany | Contract manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| NOVAFON Elektromedizinische Geraete GMBH | Weinstadt Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Physiomed Elektromedizin AG | SCHNAITTACH/LAIPERSDORF Bavaria, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Richard Wolf GMBH | KNITTLINGEN Baden-Wurttemberg, Germany | Contract manufacturer, Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Saxony Beauty Technology GMBH | Dresden Saxony, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Zimmer Medizinsysteme GMBH | NEU-ULM 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.