Skip to content

Penntack Enterprises, Inc.

Country not established

Devices
1

What Penntack Enterprises, Inc. makes

Penntack Enterprises, Inc. manufactures the Cosmelight, a device designed for aesthetic skin treatments, including non-invasive light-based therapies for rejuvenation and pigmentation correction.

The Cosmelight is classified as a Class II medical device in the US 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

  • Cosmelight Ref K061720

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

Frequently asked questions

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

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

Which registries list Penntack Enterprises, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Penntack Enterprises, Inc. include COSMELIGHT.

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