Kleengel, LLC is one of 18945 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Kleengel, LLC - FDA 510(k) Cleared Devices
Recent clearances: KleenGel Dispenser
1
Total
1
Cleared
0
Denied
Kleengel, LLC has 1 FDA 510(k) cleared medical devices. Based in Boca Raton, US.
Historical record: 1 cleared submissions from 2015 to 2015. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Kleengel, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mdi Consultants, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Kleengel, LLC
1 devices