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Camdent Laboratories

Country not established

Devices
1

What Camdent Laboratories makes

Camdent Laboratories produces denture adjustment kits designed for modifying and fitting dentures to improve patient comfort and occlusion.

The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Denture Adjustment Kit Ref K820685

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

Frequently asked questions

How many devices does Camdent Laboratories have in the registry?

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

Which registries list Camdent Laboratories's devices?

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

What risk classes do Camdent Laboratories's devices fall under?

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

What are the newest devices from Camdent Laboratories in the registry?

The most recently registered devices listed for Camdent Laboratories include DENTURE ADJUSTMENT KIT.

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