Glaukos Corporation - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Glaukos Corporation has 1 FDA 510(k) cleared medical devices. Based in San Clemente, US.
Last cleared in 2022. Active since 2022. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Glaukos Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Glaukos Corporation
1 devices