Data / Medical devices / Germany / Braun GmbH
Braun GmbH: FDA-registered device maker in Schwalbach/Ts Hesse, Germany, 2 510(k) clearances
Braun GmbH is registered with the FDA (registration 3039398006) in Schwalbach/Ts Hesse, Germany. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated June 5, 2006. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3039398006
- Address
- Sulzbacher Str. 40, Schwalbach/Ts Hesse, Germany, 65824
- Owner or operator
- Procter & Gamble (9915005)
- Roles
- Specification developer
- First device listed
- December 6, 2007
- Registered through
- 2026
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Toothbrush, Powered | JEQ | 1 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| June 5, 2006 | K061351 | ORAL-B SONIC COMPLETE | JEQ | Substantially Equivalent | Braun GmbH | accessdata.fda.gov |
| May 31, 2006 | K061199 | ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES | JEQ | Substantially Equivalent | Braun GmbH | accessdata.fda.gov |
Compare with other makers
Updated June 5, 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.