Pentron Clinical is one of 5195 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pentron Clinical - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Pentron Clinical has 4 FDA 510(k) cleared medical devices. Based in Orange, US.
Historical record: 4 cleared submissions from 2011 to 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Pentron Clinical Filter by specialty or product code using the sidebar.
Pentron Clinical — FDA 510(k) Products and Clearance History
4 devices
Cleared
Jul 02, 2013
CORRECT PLUS 1
Dental
90d
Cleared
May 22, 2012
TEMPSPAN CLEAR MATRIX
Dental
140d
Cleared
Aug 01, 2011
B1P ADHESIVE
Dental
70d
Cleared
Jan 05, 2011
BUILD-IT TOTAL CORE
Dental
107d