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Epilator Corp.

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Devices
1

What Epilator Corp. makes

Epilator Corp. manufactures the KENATRON Epilator, a handheld device designed for hair removal through electrolysis.

The KENATRON Epilator 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, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Kenatron Epilator Ref K761049

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

Frequently asked questions

How many devices does Epilator Corp. have in the registry?

The registry currently lists 1 device for Epilator Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Epilator Corp.'s devices?

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

What risk classes do Epilator Corp.'s devices fall under?

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

What are the newest devices from Epilator Corp. in the registry?

The most recently registered devices listed for Epilator Corp. include KENATRON EPILATOR.

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