Luma Vision Limited is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Luma Vision Limited - FDA 510(k) Cleared Devices
Recent clearances: VERAFEYE System VERAFEYE Imaging Catheter & VERAFEYE Imaging System
2
Total
2
Cleared
0
Denied
Luma Vision Limited has 2 FDA 510(k) cleared medical devices. Based in Dublin, IE.
Latest FDA clearance: Jun 2026. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Luma Vision Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Luma Vision Limited
2 devices