FDA Device Intelligence
HomeDevice types › MFD

Cannula, Intrauterine Insemination

FDA product code MFD · Class 2 · Obstetrics/Gynecology

32
Registered devices
4
Adverse events
1
Recalls
29
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2020-02-28CooperSurgical, Inc.Expiration date discrepancy. Marked as 5 years. Expiration date should be 3 years.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.