FDA applicant

Artron Laboratories, Inc.

Burnaby, British Columbia, CA1 decision2006–20060 recalls

FDA records 1 decision for Artron Laboratories, Inc. (Burnaby, British Columbia, CA) in 2006: 1 510(k) clearance. All are in product code LCX (Kit, Test, Pregnancy, Hcg, Over The Counter). 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 Artron Laboratories, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Artron Laboratories, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Artron Laboratories, Inc.

Which product codes does it file in?

What has FDA decided for it lately?