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Dent'N CO

Country not established

Devices
1

What Dent'N CO makes

Dent’N CO manufactures the I LIGHT, a dental curing light designed for precision polymerization of composite resins and adhesives in clinical settings.

The I LIGHT 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, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • I Light Ref K072807

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

Frequently asked questions

How many devices does Dent'N CO have in the registry?

The registry currently lists 1 device for Dent'N CO. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dent'N CO's devices?

Among its 1 most recently registered device, Dent'N CO has devices listed in FDA 510(k) (1 device).

What risk classes do Dent'N CO's devices fall under?

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

What are the newest devices from Dent'N CO in the registry?

The most recently registered devices listed for Dent'N CO include I LIGHT.

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