Kimberly Clark Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kimberly Clark Corporation - FDA 510(k) Cleared Devices
Recent clearances: KIMTECH™ Polaris™ Xtra Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate, Simulated Gastric Acid and Fentanyl in Simulated Gastric Acid, KIMTECH™ Polaris™ Nitrile Powder-Free Exam Gloves Tested for Use with Chemotherapy Drugs, Opioid Fentanyl Citrate, Simulated Gastric Acid and Fentanyl in Simulated Gastric Acid, U by Kotex® Click® Unscented Menstrual Tampons
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.
Regulatory submissions have been managed by Truscott Medsci Associates, LLC and Pathmaker FDA Law, PLLC.