FDA applicant

Lifepoint,Inc

Ontario, CA3 decisions1984–20040 recalls

FDA records 3 decisions for Lifepoint,Inc (Ontario, CA) from 1984 to 2004: 3 510(k) clearances. Most are in product codes DJG (Enzyme Immunoassay, Opiates) and LIX (Aid, Cardiopulmonary Resuscitation). 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 Lifepoint,Inc’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Lifepoint,Inc since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Lifepoint,Inc

Which product codes does it file in?

What has FDA decided for it lately?