# Conceptus, Inc.

- Location (FDA's records): San Carlos, CA
- FDA decisions: 9 (1994–1998): 9 510(k) clearances
- Product codes: MKO (2), LKF (2), HIH (2), MFD (1), HET (1), MOV (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 1 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms that cite its devices most
- Femdx Medsystems, Inc.: 1 (https://510kreport.com/company/femdx-medsystems)

## Its most-cited devices
- K962587: Conceptus Fallopian Tube Catheteization with Microendoscopy System (1997), cited by 1

## Recent decisions
- K974028: Stargate Falloposcopy Catheter, Trifurcated Irrigation Tubing (Jan 21, 1998)
- K972210: Resectoscope Safety Sheath (Sep 5, 1997)
- K962587: Conceptus Fallopian Tube Catheteization with Microendoscopy System (Jan 31, 1997)
- K954164: Hysteroscope (Mar 12, 1996)
- K953314: Conceptus Fallopian Tube Catheterization System (Jul 28, 1995)
- K932387: Conceptus Vari-Soft Cath/Pirouette Posit Mandrel (Mar 6, 1995)
- K932993: Intrauterine Catheter and Introducer (Jan 6, 1995)
- K933723: Conceptus Uterine Catheter (Dec 27, 1994)

Source page: https://510kreport.com/company/conceptus