Technolas Perfect Vision GmbH - FDA 510(k) Cleared Devices

Technolas Perfect Vision GmbH has 10 FDA 510(k) cleared ophthalmic devices. Based in Anaheim, US.

Historical record: 10 cleared submissions from 1999 to 2020.

Browse the complete list of FDA 510(k) cleared ophthalmic devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Technolas Perfect Vision GmbH / Institution Name as regulatory consultant.