Ivoclar Vivadent, Agin is one of 5240 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Ivoclar Vivadent, Agin - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Ivoclar Vivadent, Agin has 1 FDA 510(k) cleared medical devices. Based in Amherst, US.
Historical record: 1 cleared submissions from 2013 to 2013. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Ivoclar Vivadent, Agin Filter by specialty or product code using the sidebar.
Ivoclar Vivadent, Agin — FDA 510(k) Products and Clearance History
1 devices