Glaukos Corporation is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Glaukos Corporation - FDA 510(k) Cleared Devices
Recent clearances: iStent infinite Trabecular Micro-Bypass System, Model iS3
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.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Glaukos Corporation
1 devices