Skip to content

Lois Yee Cosmetics, Inc.

Country not established

Devices
1

What Lois Yee Cosmetics, Inc. makes

Lois Yee Cosmetics, Inc. manufactures the EPILATOR 8500, a device designed for hair removal through electrolysis.

The EPILATOR 8500 is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. 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

  • Epilator 8500 Ref K851413

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

Frequently asked questions

How many devices does Lois Yee Cosmetics, Inc. have in the registry?

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

Which registries list Lois Yee Cosmetics, Inc.'s devices?

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

What risk classes do Lois Yee Cosmetics, Inc.'s devices fall under?

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

What are the newest devices from Lois Yee Cosmetics, Inc. in the registry?

The most recently registered devices listed for Lois Yee Cosmetics, Inc. include EPILATOR 8500.

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