Pentron Laboratory Technologies is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pentron Laboratory Technologies - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Pentron Laboratory Technologies has 5 FDA 510(k) cleared medical devices. Based in Wallingford, US.
Historical record: 5 cleared submissions from 2002 to 2003. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Pentron Laboratory Technologies Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pentron Laboratory Technologies
5 devices