Sybron Endo/Analytic is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Sybron Endo/Analytic - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Sybron Endo/Analytic has 3 FDA 510(k) cleared medical devices. Based in Orange, US.
Historical record: 3 cleared submissions from 2002 to 2004. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Sybron Endo/Analytic Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Sybron Endo/Analytic
3 devices