Pentron Clinical is one of 5670 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.
FDA 510(k) Regulatory Record - Pentron Clinical
4 devices