FDA applicant

Conceptus, Inc.

San Carlos, CA9 decisions1994–19980 recalls

FDA records 9 decisions for Conceptus, Inc. (San Carlos, CA) from 1994 to 1998: 9 510(k) clearances. Most are in product codes MKO (Falloposcope) and LKF (Cannula, Manipulator/Injector, Uterine). 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 Conceptus, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Conceptus, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Conceptus, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Conceptus, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?