LivaNova USA, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
LivaNova USA, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Venous Return Cannulae, RAP Femoral Venous Cannulae, SMARxT Tubing and Connectors
3
Total
3
Cleared
0
Denied
LivaNova USA, Inc. has 3 FDA 510(k) cleared medical devices. Based in Arvada, US.
Latest FDA clearance: Mar 2026. Active since 2024. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by LivaNova USA, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Sorin Group Italia S.R.L. as regulatory consultant.
FDA 510(k) Regulatory Record - LivaNova USA, Inc.
3 devices