Limbus Ai, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Limbus Ai, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Limbus Contour, Limbus Contour, Limbus Contour
3
Total
3
Cleared
0
Denied
Limbus Ai, Inc. has 3 FDA 510(k) cleared medical devices. Based in Regina, CA.
Latest FDA clearance: Oct 2024. Active since 2020. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Limbus Ai, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Medical Device Academy as regulatory consultant.
FDA 510(k) Regulatory Record - Limbus Ai, Inc.
3 devices