Eyeq, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eyeq, Inc. - FDA 510(k) Cleared Devices
Recent clearances: EyeQ nanoECP
1
Total
1
Cleared
0
Denied
Eyeq, Inc. has 1 FDA 510(k) cleared medical devices. Based in Reno, US.
Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Eyeq, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Eyeq, Inc.
1 devices