FDA applicant

Alladin Diagnostic, Inc.

Princeton, NJ2 decisions1983–19850 recalls

FDA records 2 decisions for Alladin Diagnostic, Inc. (Princeton, NJ) from 1983 to 1985: 2 510(k) clearances. Most are in product codes JGG (L-Leucine-4-Nitroanilide (Colorimetric)…) and KQE (Assay, Erythrocytic Glucose-6-Phosphate…). 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 Alladin Diagnostic, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Alladin Diagnostic, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Alladin Diagnostic, Inc.

Which product codes does it file in?

What has FDA decided for it lately?