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Bfw Laboratories, Inc.

United StatesFDA applicant, unverified

Devices
2

What Bfw Laboratories, Inc. makes

Bfw Laboratories, Inc. makes the S.E.T. Tube and the BFW Voice Generator.

These devices are classified as Class II and are listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • S.E.T. Tube Ref K843988

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Bfw Voice Generator Ref K851462

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

Frequently asked questions

How many devices does Bfw Laboratories, Inc. have in the registry?

The registry currently lists 2 devices for Bfw Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Bfw Laboratories, Inc.'s devices?

Among its 2 most recently registered devices, Bfw Laboratories, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Bfw Laboratories, Inc.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Bfw Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Bfw Laboratories, Inc. in the registry?

The most recently registered devices listed for Bfw Laboratories, Inc. include S.E.T. TUBE and BFW VOICE GENERATOR.

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