510(k) Report

FDA applicant

Diamond General Development Corp.

Ann Arbor, MI1 decision1998–19980 recalls

FDA records 1 decision for Diamond General Development Corp. (Ann Arbor, MI) in 1998: 1 De Novo grant. All are in product code MVH (Device, Detection, Sulfide). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, dental panel, where it files most

How often FDA has decided Diamond General Development Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diamond General Development Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Diamond General Development Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • MVHDevice, Detection, Sulfide1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • DEN980003Diamond Probe/Perio 2000 SystemDiamond General Development Corp. · 19981cites it

What has FDA decided for it lately?

  • DEN980003Diamond Probe/Perio 2000 SystemDiamond General Development Corp. · 1998

The one decision as Diamond General Development Corp. →

Other applicant names beginning “Diamond”

FDA records each applicant name separately; these may or may not be the same firm.

Diamond Diagnostics, Inc. 26Diamond Medical, Inc. 6Diamond Sensor Systems 3Diamond Medical Equipment, Inc. 3Diamond Shamrock Corp. 2Diamond Electro-Tech, Inc. 1Diamond Orthopedic, LLC 1Diamond Rotary and Carbide Intl. 1Diamond Systems USA, Inc. 1Diamond Age Systems, Inc. 1Diamond Orthotic Laboratory 1Diamond Mark International Co., Ltd. 1