Beavers Dental, Div. Sybron Canada, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Beavers Dental, Div. Sybron Canada, Ltd. - FDA 510(k) Cleared Devices
3
Total
3
Cleared
0
Denied
Beavers Dental, Div. Sybron Canada, Ltd. has 3 FDA 510(k) cleared medical devices. Based in Washington, US.
Historical record: 3 cleared submissions from 1986 to 2012. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Beavers Dental, Div. Sybron Canada, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Beavers Dental, Div. Sybron Canada, Ltd.
3 devices