Cubresa, Inc. is one of 411 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Cubresa, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cubresa BrainPET
1
Total
1
Cleared
0
Denied
Cubresa, Inc. has 1 FDA 510(k) cleared medical devices. Based in Winnipeg, CA.
Latest FDA clearance: Jul 2026. Active since 2026. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Cubresa, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Device Pathways, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Cubresa, Inc.
1 devices