Wavelight AG is one of 234 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Wavelight AG - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Wavelight AG has 1 FDA 510(k) cleared medical devices. Based in Erlangen, DE.
Historical record: 1 cleared submissions from 2007 to 2007. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Wavelight AG Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Wavelight AG
1 devices