Perio-Giene is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Perio-Giene - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Perio-Giene has 1 FDA 510(k) cleared medical devices. Based in Redwood City, US.
Historical record: 1 cleared submissions from 1993 to 1993. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Perio-Giene Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Perio-Giene
1 devices