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Diamond General Development Corp.

Country not established

Devices
1

What Diamond General Development Corp. makes

Diamond General Development Corp. manufactures the Diamond Probe/Perio 2000 System, a periodontal probing device used for measuring pocket depths in dental examinations.

The company’s portfolio is regulated under FDA Class II devices and is listed via the 510(k) pathway. The manufacturer 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

  • Diamond Probe/Perio 2000 System Ref DEN980003

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

Frequently asked questions

How many devices does Diamond General Development Corp. have in the registry?

The registry currently lists 1 device for Diamond General Development Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Diamond General Development Corp.'s devices?

Among its 1 most recently registered device, Diamond General Development Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Diamond General Development Corp.'s devices fall under?

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

What are the newest devices from Diamond General Development Corp. in the registry?

The most recently registered devices listed for Diamond General Development Corp. include DIAMOND PROBE/PERIO 2000 SYSTEM.

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