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Dental Alloy Products, Inc.

United StatesFDA applicant, unverified

Devices
5

What Dental Alloy Products, Inc. makes

Dental Alloy Products, Inc. manufactures a series of dental alloy devices identified as SUPER 1, SUPER 3, SUPER 6, SUPER 12, and SUPER 14, which are used in restorative and prosthetic dental applications.

All of these devices are classified as Class II medical devices and are listed in the FDA 510(k) database. The company is based in the United States.

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

Catalogue5

Newest first, rows 1-5 of 5

  • Super 12 Ref K002301

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

  • Super 6 Ref K002300

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

  • Super 14 Ref K002302

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

  • Super 3 Ref K002299

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

  • Super 1 Ref K002298

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

Frequently asked questions

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

The registry currently lists 5 devices for Dental Alloy Products, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dental Alloy Products, Inc.'s devices?

Among its 5 most recently registered devices, Dental Alloy Products, Inc. has devices listed in FDA 510(k) (5 devices).

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

Among its 5 most recently registered devices, the classes recorded for Dental Alloy Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Dental Alloy Products, Inc. include SUPER 12, SUPER 6, SUPER 14 and SUPER 3.

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