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The Braun Corp.

Country not established

Devices
1
FDA recalls
3

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What The Braun Corp. makes

The Braun Corp. makes the BRAUN DENTAL CENTER OC-3, a dental device used in clinical settings for dental procedures.

This device is classified as Class I and is listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Braun Dental Center Oc-3 Ref K844339

    Active Regimes: 510(k) Registry: 510(k) Class:I

FDA recalls3

Recalls are matched to the firm by name. FDA recall data as of 1 Nov 2026.

FDA recall records list 3 recalls initiated by The Braun Corp., initiated on 2007-08-15. By recorded status: 3 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2007

    • 15 Aug 2007 Z-2467-2010 Unclassified (pre-2012) Terminated The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured. Distribution: Worldwide distribution Submission number: K952946
    • 15 Aug 2007 Z-2468-2010 Unclassified (pre-2012) Terminated The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured. Distribution: Worldwide distribution Submission number: K952946
    • 15 Aug 2007 Z-2469-2010 Unclassified (pre-2012) Terminated The wheelchair lifts threshold warning system may not operate and the wheelchair user can fall from the vehicle and be seriously injured. Distribution: Worldwide distribution Submission number: K952946

Frequently asked questions

How many devices does The Braun Corp. have in the registry?

The registry currently lists 1 device for The Braun Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list The Braun Corp.'s devices?

Among its 1 most recently registered device, The Braun Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do The Braun Corp.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for The Braun Corp.'s devices are Class I. Each device page shows its own class and authorisation.

Are there FDA recall records for The Braun Corp.?

FDA recall records list 3 recalls initiated by The Braun Corp., the most recent initiated on 15 Aug 2007. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from The Braun Corp. in the registry?

The most recently registered devices listed for The Braun Corp. include BRAUN DENTAL CENTER OC-3.

Generated automatically from registry data and not verified by a human reviewer.