Nova Eye, Inc. is one of 12968 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nova Eye, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Nova Eye iTrack™ 250A Canaloplasty Microcatheter (iTrack™ 250A)
1
Total
1
Cleared
0
Denied
Nova Eye, Inc. has 1 FDA 510(k) cleared medical devices. Based in Fremont, US.
Latest FDA clearance: Aug 2026. Active since 2026. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Nova Eye, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nova Eye, Inc.
1 devices