FDA applicant

Modular Diagnostic Systems, Inc.

Syracuse, NY1 decision1988–19880 recalls

FDA records 1 decision for Modular Diagnostic Systems, Inc. (Syracuse, NY) in 1988: 1 510(k) clearance. All are in product code JJE (Analyzer, Chemistry (Photometric, Discrete)…). 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 Modular Diagnostic Systems, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Modular Diagnostic Systems, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Modular”

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

Modular Medical, Inc. 3 Modular Cutting Systems, Inc. 2 Modular Instruments, Inc. 1 Modular X-Ray Devices 1

Modular Diagnostic Systems, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Modular”