Eyenuk, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eyenuk, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EyeArt v2.2.0, EyeArt
2
Total
2
Cleared
0
Denied
Eyenuk, Inc. has 2 FDA 510(k) cleared medical devices. Based in Los Angeles, US.
Last cleared in 2023. Active since 2020. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Eyenuk, Inc. Filter by specialty or product code using the sidebar.
2 devices have linked clinical trials registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Eyenuk, Inc.
2 devices