Kardium, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Kardium, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Globe® Pulsed Field System, Globe Introducer (601-01001)
2
Total
2
Cleared
0
Denied
Kardium, Inc. has 2 FDA 510(k) cleared medical devices. Based in Burnaby, CA.
Latest FDA clearance: Jun 2025. Active since 2025. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Kardium, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kardium, Inc.
2 devices