FDA applicant

Serex, Inc.

Tenafly, NJ5 decisions1989–19920 recalls

FDA records 5 decisions for Serex, Inc. (Tenafly, NJ) from 1989 to 1992: 5 510(k) clearances. Most are in product codes JZG (System, Test, Beta-2-Microglobulin Immunological) and DIO (Enzyme Immunoassay, Cocaine And Cocaine…). 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 toxicology panel, where it files most

How often FDA has decided Serex, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Serex, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Serex, Inc.

Which product codes does it file in?

What has FDA decided for it lately?