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Dental Services, Inc.

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Devices
1

What Dental Services, Inc. makes

Dental Services, Inc. manufactures the PROPAK, a dental device designed for use in oral health procedures, including dental impressions and molds.

The PROPAK is classified as a Class II medical device under US regulations and is listed in the FDA’s 510(k) registry. 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

  • Propak Ref K924118

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

Frequently asked questions

How many devices does Dental Services, Inc. have in the registry?

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

Which registries list Dental Services, Inc.'s devices?

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

What risk classes do Dental Services, Inc.'s devices fall under?

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

What are the newest devices from Dental Services, Inc. in the registry?

The most recently registered devices listed for Dental Services, Inc. include PROPAK.

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