KXP · Class II · 21 CFR 884.3900

FDA Product Code KXP: Stent, Vaginal

Leading manufacturers include Pmt Corporation, Silimed, LLC and Owen Mumford USA, Inc..

4
Total
4
Cleared
433d
Avg days
1995
Since

FDA 510(k) Cleared Stent, Vaginal Devices (Product Code KXP)

4 devices
1–4 of 4
Cleared Sep 30, 2020
Allura Vaginal Stent
K202542
Pmt Corporation
Obstetrics & Gynecology · 28d
Cleared Nov 25, 1998
AMIELLE
K983045
Owen Mumford USA, Inc.
Obstetrics & Gynecology · 85d
Cleared Aug 05, 1998
SILIMED VAGINAL STENT
K974479
Silimed, LLC
Obstetrics & Gynecology · 252d

About Product Code KXP - Regulatory Context