FDA Device Intelligence
HomeDevice types › HDX

Dilator, Vaginal

FDA product code HDX · Class 2 · Obstetrics/Gynecology

66
Registered devices
4
Adverse events
1
Recalls
9
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2015-06-19CooperSurgical, Inc.Incorrect expiration date on outer carton kit label

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.