Eyenez, LLC is one of 13008 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eyenez, LLC - FDA 510(k) Cleared Devices
Recent clearances: Eyenez Ophthalmic Camera
1
Total
1
Cleared
0
Denied
Eyenez, LLC has 1 FDA 510(k) cleared medical devices. Based in Pasadena, US.
Historical record: 1 cleared submissions from 2016 to 2016. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Eyenez, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Accurate Consultants, Inc. as regulatory consultant. 1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Eyenez, LLC
1 devices