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Dongguan Yanxi Technology Co., Ltd.

ChinaFDA 510(k) applicant, unverified FDA

Devices
1
Registrations
FDA
FDA recalls
0

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA establishment

What Dongguan Yanxi Technology Co., Ltd. makes

Dongguan Yanxi Technology Co., Ltd. makes medical devices such as the LED Light Therapy Mask, which falls under device categories 2311, 2344, 2457, and 2458.

The company's portfolio is regulated as Class II devices and is listed in the fda_510k registry, with the company based in the US.

AI-generated from registry data, 26 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Dongguan Yanxi Technology Co. Ltd. Dongguan Guangdong · CN FEI 3017618922

Frequently asked questions

How many devices does Dongguan Yanxi Technology Co., Ltd. have in the registry?

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

Which registries list Dongguan Yanxi Technology Co., Ltd.'s devices?

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

What risk classes do Dongguan Yanxi Technology Co., Ltd.'s devices fall under?

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

What are the newest devices from Dongguan Yanxi Technology Co., Ltd. in the registry?

The most recently registered devices listed for Dongguan Yanxi Technology Co., Ltd. include LED Light Therapy Mask (2311, 2344, 2457, 2458).

Which FDA establishments are linked to Dongguan Yanxi Technology Co., Ltd.?

1 FDA establishment is linked to Dongguan Yanxi Technology Co., Ltd. in the registry; they are listed on the company page.

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