Kimberly-Clark Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kimberly-Clark Corp. - FDA 510(k) Cleared Devices
Recent clearances: KIMGUARD SMART-FOLD STERILIZATION WRAP, U BY KOTEX SECURITY UNSCENTED MENSTRUAL TAMPONS, KC 300 SURGICAL MASK
104
Total
103
Cleared
0
Denied
Kimberly-Clark Corp. has 103 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 103 cleared submissions from 1978 to 2014. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Kimberly-Clark Corp. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Kimberly-Clark Corp.
104 devices
Cleared
Nov 10, 2014
KIMGUARD SMART-FOLD STERILIZATION WRAP
General Hospital
209d
Cleared
Aug 25, 2014
U BY KOTEX SECURITY UNSCENTED MENSTRUAL TAMPONS
Obstetrics & Gynecology
98d
Cleared
Dec 20, 2013
KC 300 SURGICAL MASK
General Hospital
179d
Cleared
Nov 07, 2013
KIMBERLY-CLARK LAVENDER NITRILE POWDER-FREE EXAM GLOVE
General Hospital
139d
Cleared
Aug 20, 2013
KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING ENDOTRACHEAL TUBE
Anesthesiology
110d
Cleared
Dec 19, 2012
KIMVENT MICROCUFF SUBGLOTTIC SUCTIONING
Anesthesiology
261d
Cleared
Jun 22, 2012
KIMGUARD ONE-STEP STERILIZATION WRAP
General Hospital
269d
Cleared
Mar 09, 2012
KIMBERLY CLARK PURPLE NITRILE, AND PURPLE NITRILE XTRA POWDER FREE EXAM GLOVE
General Hospital
109d
Cleared
Jan 19, 2012
KIMGUARD SMART-FOLD* STERILIZATION WRAP
General Hospital
162d
Cleared
Oct 07, 2011
U BY KOTEX SLEEK UNSCENTED MENSTRUAL TAMPONS
Obstetrics & Gynecology
28d
Cleared
Apr 29, 2011
KIMBERLY-CLARK LOW BARRIER, ASTM 2100 FACE MASKS
General Hospital
73d
Cleared
Dec 23, 2010
MICROCOOL BREATHABLE HIGH PERFORMANCE SURGICAL GOWNS
General Hospital
34d
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