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Data / Medical devices / Germany / Braun GMBH

Braun GMBH: FDA-registered device maker in KRONBERG Hesse, Germany, 2 510(k) clearances

Braun GMBH is registered with the FDA (registration 9617642) in KRONBERG Hesse, Germany. It lists 2 device types. The FDA files 2 510(k) clearances under its listings, the newest dated June 5, 2006. Registered through 2027. FDA data exported November 2, 2026.

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FDA registration number
9617642
FEI number
1000227535
Address
Frankfurter Strasse 145, KRONBERG Hesse, Germany, D61476
Owner or operator
Procter & Gamble (9915005)
Roles
Specification developer
First device listed
July 30, 2001
Registered through
2027

Devices it lists

DeviceProduct codeClassRoleSource
Toothbrush, ManualEFW1Specification developeraccessdata.fda.gov
Toothbrush, PoweredJEQ1Specification developeraccessdata.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.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
June 5, 2006K061351ORAL-B SONIC COMPLETEJEQSubstantially EquivalentBraun GmbHaccessdata.fda.gov
May 31, 2006K061199ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIESJEQSubstantially EquivalentBraun GmbHaccessdata.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.