510(k) Report

FDA applicant

Diamond Rotary and Carbide Intl.

Canada R3c 4e5, CA1 decision1990–19900 recalls

FDA records 1 decision for Diamond Rotary and Carbide Intl. (Canada R3c 4e5, CA) in 1990: 1 510(k) clearance. All are in product code DZP (Instrument, Diamond, Dental). 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 Rotary and Carbide Intl.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diamond Rotary and Carbide Intl. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Diamond Rotary and Carbide Intl. 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?

  • DZPInstrument, Diamond, Dental1decision

What has FDA decided for it lately?

  • K901262F.G. Laser (Dental Bur)Diamond Rotary and Carbide Intl. · 1990

The one decision as Diamond Rotary and Carbide Intl. →

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 Systems USA, Inc. 1Diamond Age Systems, Inc. 1Diamond General Development Corp. 1Diamond Orthotic Laboratory 1Diamond Mark International Co., Ltd. 1