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Zuko, Inc.

Country not established

Devices
1

What Zuko, Inc. makes

Zuko, Inc. manufactures the Acne Light Therapy Wand, a handheld device designed for targeted light therapy to treat acne. The product is intended for at-home use and employs specific wavelengths of light to address skin conditions.

The Acne Light Therapy Wand is classified as a Class II medical device in the US and is authorised through the FDA’s 510(k) pathway. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Acne Light Therapy Wand Ref K160691

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

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

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

Which registries list Zuko, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Zuko, Inc. include Acne Light Therapy Wand.

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