FDA applicant

Ceres Fertility, Inc.

Irvine, CA2 decisions2002–20030 recalls

FDA records 2 decisions for Ceres Fertility, Inc. (Irvine, CA) from 2002 to 2003: 2 510(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 Ceres Fertility, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ceres Fertility, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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See the 510(k) Report

Other applicant names beginning “Ceres”

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

Ceres Medical Systems, LLC 1

Ceres Fertility, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ceres”