Eyekon Medical, Inc. is one of 13445 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Eyekon Medical, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Temporary Keratoprosthesis (QuickSet TKP™)
1
Total
1
Cleared
0
Denied
Eyekon Medical, Inc. has 1 FDA 510(k) cleared medical devices. Based in Clearwater, US.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Ophthalmic.
Browse the FDA 510(k) cleared devices submitted by Eyekon Medical, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Onera, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Eyekon Medical, Inc.
1 devices