MicroVention, Inc., d/b/a Terumo Neuro is one of 16286 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
MicroVention, Inc., d/b/a Terumo Neuro - FDA 510(k) Cleared Devices
Recent clearances: Mayumi™ Thrombectomy System, BOBBY Balloon Guide Catheter
2
Total
2
Cleared
0
Denied
MicroVention, Inc., d/b/a Terumo Neuro has 2 FDA 510(k) cleared medical devices. Based in Aliso Viejo, US.
Latest FDA clearance: Sep 2026. Active since 2026. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by MicroVention, Inc., d/b/a Terumo Neuro Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - MicroVention, Inc., d/b/a Terumo Neuro
2 devices