Viopti, Ltd. is one of 174 FDA 510(k) medical device manufacturers from United Kingdom in the dataset, ranked by real submission volume.
Viopti, Ltd. - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Viopti, Ltd. has 1 FDA 510(k) cleared medical devices. Based in Dumbarton, GB.
Historical record: 1 cleared submissions from 2014 to 2014. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Viopti, Ltd. Filter by specialty or product code using the sidebar.
Viopti, Ltd. — FDA 510(k) Products and Clearance History
1 devices