Procordia Oratech AB is one of 59 FDA 510(k) medical device manufacturers from Sweden in the dataset, ranked by real submission volume.
Procordia Oratech AB - FDA 510(k) Cleared Devices
1
Total
0
Cleared
0
Denied
Procordia Oratech AB has 0 FDA 510(k) cleared medical devices. Based in Huddinge, Sweden, SE.
Historical record: 0 cleared submissions from 1993 to 1993. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Procordia Oratech AB Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Procordia Oratech AB
1 devices