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The Buzzz Corp.

United StatesFDA applicant, unverified

Devices
4

What The Buzzz Corp. makes

The Buzzz Corp. manufactures Class II medical devices including PROWLER, PREVENT I, STEALTH, and INTRUDER.

These devices are listed in the FDA 510(k) registry and the company is based in the US.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue4

Newest first, rows 1-4 of 4

  • Prowler Ref K972037

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Prevent I Ref K973373

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Stealth Ref K972036

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Intruder Ref K972038

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

Frequently asked questions

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

The registry currently lists 4 devices for The Buzzz Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list The Buzzz Corp.'s devices?

Among its 4 most recently registered devices, The Buzzz Corp. has devices listed in FDA 510(k) (4 devices).

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

Among its 4 most recently registered devices, the classes recorded for The Buzzz Corp.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for The Buzzz Corp. include PROWLER, PREVENT I, STEALTH and INTRUDER.

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