510(k) Report

FDA applicant

Conception Technologies

Irvine, CA8 decisions2000–20030 recalls

FDA records 8 decisions for Conception Technologies (Irvine, CA) from 2000 to 2003: 8 510(k) clearances. Most are in product codes MQL (Media, Reproductive) and MTW (System, Water, Reproduction, Assisted, And…). 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 Conception Technologies’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Conception Technologies since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Conception”

FDA records each applicant name separately; these may or may not be the same firm.