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Shenzhen Walton Technology Co., Ltd.

ChinaFDA applicant, unverified

Devices
1

What Shenzhen Walton Technology Co., Ltd. makes

Shenzhen Walton Technology Co., Ltd. makes LED light therapy machines, including models G1, G3, G4, and G6.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

How many devices does Shenzhen Walton Technology Co., Ltd. have in the registry?

The registry currently lists 1 device for Shenzhen Walton Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Shenzhen Walton Technology Co., Ltd.'s devices?

Among its 1 most recently registered device, Shenzhen Walton Technology Co., Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Shenzhen Walton Technology Co., Ltd.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Shenzhen Walton Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Shenzhen Walton Technology Co., Ltd. in the registry?

The most recently registered devices listed for Shenzhen Walton Technology Co., Ltd. include LED Light Therapy Machine (G1, G3, G4, G6).

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