Kimberly Clark Corporation - FDA 510(k) Cleared Devices
13
Total
12
Cleared
0
Denied
Kimberly Clark Corporation has 12 FDA 510(k) cleared medical devices. Based in Neenah, US.
Last cleared in 2023. Active since 2010.
Browse the FDA 510(k) cleared devices submitted by Kimberly Clark Corporation Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Pathmaker FDA Law, PLLC as regulatory consultant.
13 devices
Cleared
Aug 28, 2023
KIMTECH™ Polaris™ Xtra Nitrile Powder-Free Exam Gloves Tested for Use with...
General Hospital
103d
Cleared
Jul 21, 2023
KIMTECH™ Polaris™ Nitrile Powder-Free Exam Gloves Tested for Use with...
General Hospital
102d
Cleared
Jan 06, 2023
U by Kotex® Click® Unscented Menstrual Tampons
Obstetrics & Gynecology
23d
Cleared
Nov 30, 2020
Kimtech Prizm Multi-Layered Exam Glove Tested for use with Chemotherapy...
General Hospital
98d
Cleared
Apr 10, 2020
KIMTECH Purple Nitrile Powder Free Examination Gloves Tested for Use with...
General Hospital
87d
Cleared
Oct 11, 2017
U by Kotex Click Unscented Menstrual Tampons
Obstetrics & Gynecology
90d
Cleared
Dec 02, 2014
ON-Q Pain Relief System, QuikBloc Over-the-Needle Catheter Set
Anesthesiology
29d
Cleared
Jun 09, 2014
AERO BLUE PERFORMANCE SURGICAL GOWN
General Hospital
97d
Cleared
Jun 26, 2013
MIC-KEY SF LOW PROFILE GASTROSTOMY TUBE AND ACCESSORIES
Gastroenterology & Urology
299d
Cleared
Jul 11, 2012
POISE PERSONAL LUBRICANT
Obstetrics & Gynecology
131d
Cleared
May 11, 2012
KIMBERLY-CLARK KIM VENT MICROCUFF ENDOTRACHEAL TUBE FOR ADULTS
Anesthesiology
179d
Cleared
Nov 02, 2011
U BY KOTEX CLICK UNSCENTED MENSTRUAL TAMPONS
Obstetrics & Gynecology
21d