510(k) Report

FDA applicant

Advanced Reproductive Technologies

Irvine, CA5 decisions2000–20000 recalls

FDA records 5 decisions for Advanced Reproductive Technologies (Irvine, CA) in 2000: 5 510(k) clearances. All are in product code MQL (Media, Reproductive). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Advanced Reproductive Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Advanced Reproductive Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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