Data / Medical devices / Germany / Otto Bock Mobility Solutions GmbH
Otto Bock Mobility Solutions GmbH: FDA-registered device maker in Koenigsee Thuringia, Germany, 1 510(k) clearance
Otto Bock Mobility Solutions GmbH is registered with the FDA (registration 3007923118) in Koenigsee Thuringia, Germany. It lists 3 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 7, 2006. Registered through 2026. FDA data exported November 2, 2026.
SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.
- FDA registration number
- 3007923118
- Address
- Lindenstrasse 13, Koenigsee Thuringia, Germany, D-07426
- Owner or operator
- Ottobock SE & Co. KGaA (8010097)
- Roles
- Complaint file establishment, Specification developer
- First device listed
- August 10, 2000
- Registered through
- 2026
- Brand names listed
- Paragolfer, Various models
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Accessories, Wheelchair | KNO | 1 | Specification developer | accessdata.fda.gov |
| Components, Wheelchair | KNN | 1 | Specification developer | accessdata.fda.gov |
| Wheelchair, Standup | IPL | 2 | Complaint file establishment | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 7, 2006 | K060936 | PARAGOLFER | IPL | Substantially Equivalent | Parabasetec, GmbH | accessdata.fda.gov |
Compare with other makers
- All makers of Accessories, Wheelchair
- All makers of Components, Wheelchair
- All makers of Wheelchair, Standup
Updated August 7, 2006. 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.