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Sunbeam Corp.

United StatesFDA applicant, unverified

Devices
3

What Sunbeam Corp. makes

Sunbeam Corp. manufactures personal wellness devices, including an ultrasonic cool spray humidifier for respiratory comfort, a cold pack (#589) for pain relief, and a powered gum massager designed to relieve jaw tension.

These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Ultrasonic Cool Spray Humidifier Ref K842275

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Cold Pack #589 Ref K801776

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Massager, Gum/Ssage Powered Gum Ref K780360

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

Frequently asked questions

How many devices does Sunbeam Corp. have in the registry?

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

Which registries list Sunbeam Corp.'s devices?

Among its 3 most recently registered devices, Sunbeam Corp. has devices listed in FDA 510(k) (3 devices).

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

Among its 3 most recently registered devices, the classes recorded for Sunbeam Corp.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Sunbeam Corp. in the registry?

The most recently registered devices listed for Sunbeam Corp. include ULTRASONIC COOL SPRAY HUMIDIFIER, COLD PACK #589 and MASSAGER, GUM/SSAGE POWERED GUM.

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