Medtronic, Ireland is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medtronic, Ireland - FDA 510(k) Cleared Devices
Recent clearances: Sprinter Legend Rapid Exchange Balloon Dilatation Catheter, Telescope Guide Extension Catheter, Liberant Thrombectomy System
7
Total
7
Cleared
0
Denied
Medtronic, Ireland has 7 FDA 510(k) cleared medical devices. Based in Shoreview, US.
Latest FDA clearance: Jan 2026. Active since 2006. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Medtronic, Ireland Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Medtronic, Ireland
7 devices
Cleared
Jan 17, 2026
Sprinter Legend Rapid Exchange Balloon Dilatation Catheter
Cardiovascular
205d
Cleared
Oct 29, 2025
Telescope Guide Extension Catheter
Cardiovascular
90d
Cleared
Jun 11, 2025
Liberant Thrombectomy System
Cardiovascular
89d
Cleared
Apr 09, 2013
ATTAIN COMMAND+SUREVALVE LEFT HEART DELIVERY SYSTEM ATTAIN COMMAND GUIDE...
Cardiovascular
182d
Cleared
Oct 22, 2010
SPRINTER LEGEND 1.25MM RX AND SPRINTER LEGEND 1.25MM OTW BALLOON
Cardiovascular
14d
Cleared
Aug 21, 2006
ATTAIN 6227DEF DEFLECTABLE CATHETER DELIVERY SYSTEM
Cardiovascular
83d
Cleared
Mar 16, 2006
ATTAIN SELECT II 6248DEL DELIVERY CATHETER SYSTEM
Cardiovascular
97d