Data / Medical devices / Components, Wheelchair / Germany
FDA-registered makers of Components, Wheelchair in Germany: 5 establishments
5 establishments in Germany are registered with the FDA to make Components, Wheelchair (product code KNN). 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
- Components, Wheelchair
- Product code
- KNN
- Country
- Germany
Makers of Components, Wheelchair in Germany
| Maker | Location | Role | 510(k) clearances | Latest clearance | PMA approvals | Recall events | Class I | Source |
|---|---|---|---|---|---|---|---|---|
| Hoggi GMBH | RANSBACH-BAUMBACH Rhineland-Palatinate, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| HomeBraceGermany GmbH | Urbach Baden-Wurttemberg, Germany | Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Munevo GMBH | Munich Bavaria, Germany | Complaint file establishment, Manufacturer | 0 | 0 | 1 | 0 | api.fda.gov | |
| Otto Bock Manufacturing Konigsee GmbH | Koenigsee Thuringia, Germany | Contract manufacturer, Exporter to the US, Manufacturer | 0 | 0 | 0 | 0 | api.fda.gov | |
| Otto Bock Mobility Solutions GmbH | Koenigsee Thuringia, 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.