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The Gillette Company

Country not established

Devices
3

What The Gillette Company makes

The company manufactures disposable and rechargeable electric shavers, including cordless whirlpool models, as well as heat and cold wraps for muscle recovery and pain relief.

These products are classified as Class II medical devices in the US and are listed under the FDA’s 510(k) premarket notification process. The manufacturer is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Deluxe Heat Wrap/Cold Wrap Ref K801081

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Gillette Heat Wrap Ref K790374

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Gillette Cordless Whirlpool Ref K791603

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

Frequently asked questions

How many devices does The Gillette Company have in the registry?

The registry currently lists 3 devices for The Gillette Company. Devices recorded under merged duplicate company entries are counted once.

Which registries list The Gillette Company's devices?

Among its 3 most recently registered devices, The Gillette Company has devices listed in FDA 510(k) (3 devices).

What risk classes do The Gillette Company's devices fall under?

Among its 3 most recently registered devices, the classes recorded for The Gillette Company's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from The Gillette Company in the registry?

The most recently registered devices listed for The Gillette Company include DELUXE HEAT WRAP/COLD WRAP, GILLETTE HEAT WRAP and GILLETTE CORDLESS WHIRLPOOL.

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