FDA applicant

Diamond Sensor Systems

Ann Arbor, MI3 decisions1987–19880 recalls

FDA records 3 decisions for Diamond Sensor Systems (Ann Arbor, MI) from 1987 to 1988: 3 510(k) clearances. Most are in product codes JJE (Analyzer, Chemistry (Photometric, Discrete)…) and DRY (Monitor, Blood-Gas, On-Line, Cardiopulmonary…). 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, clinical chemistry panel, where it files most

How often FDA has decided Diamond Sensor Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Diamond Sensor Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Diamond”

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

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

Diamond Sensor Systems

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Diamond”