Reckitt Benckiser, LLC - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Reckitt Benckiser, LLC has 5 FDA 510(k) cleared medical devices. Based in Parsippany, US.
Historical record: 5 cleared submissions from 2014 to 2018. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Reckitt Benckiser, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Reckitt Benckiser, LLC
5 devices
Cleared
Jan 12, 2018
K-Y Silicone
Obstetrics & Gynecology
60d
Cleared
Jan 11, 2016
K-Y Marilyn Pleasure Gel
Obstetrics & Gynecology
186d
Cleared
Jul 31, 2015
Durex Silicone
Obstetrics & Gynecology
231d
Cleared
Dec 17, 2014
DUREX REALFEEL PLEASURE GEL PERSONAL LUBRICANT
Obstetrics & Gynecology
560d
Cleared
Nov 04, 2014
DUREX EMBRACE PERSONAL LUBRICANT
Obstetrics & Gynecology
281d