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Cheung Laboratories, Inc.

Country not established

Devices
1

What Cheung Laboratories, Inc. makes

Cheung Laboratories, Inc. manufactures diathermy devices designed for microfocus applications, which deliver controlled thermal energy for localized tissue treatment.

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

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Diathermy Device-Microfocus Ref K941567

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

Frequently asked questions

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

The registry currently lists 1 device for Cheung Laboratories, Inc.. Devices recorded under merged duplicate company entries are counted once.

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

Among its 1 most recently registered device, Cheung Laboratories, Inc. has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for Cheung Laboratories, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Cheung Laboratories, Inc. include DIATHERMY DEVICE-MICROFOCUS.

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