Neuravi Limited is one of 55 FDA 510(k) medical device manufacturers from Ireland in the dataset, ranked by real submission volume.
Neuravi Limited - FDA 510(k) Cleared Devices
Recent clearances: EMBOTRAP III Revascularization Device, EMBOGUARD Balloon Guide Catheter, EMBOGUARD Balloon Guide Catheter
3
Total
3
Cleared
0
Denied
Neuravi Limited has 3 FDA 510(k) cleared medical devices. Based in Galway, IE.
Latest FDA clearance: Sep 2025. Active since 2021. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neuravi Limited Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Neuravi Limited
3 devices