FDA applicant

Toxi-Lab, Inc.

Irvine, CA5 decisions1990–19930 recalls

FDA records 5 decisions for Toxi-Lab, Inc. (Irvine, CA) from 1990 to 1993: 5 510(k) clearances. Most are in product codes DML (Nad-Nadh, Specific Reagent For Alcohol Enzyme…) and DIF (Drug Mixture Control Materials). 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 Toxi-Lab, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Toxi-Lab, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Toxi-Lab, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Toxi-Lab, Inc.

Which product codes does it file in?

What has FDA decided for it lately?