Geneseeq Technology, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Geneseeq Technology, Inc. - FDA 510(k) Cleared Devices
Recent clearances: GENESEEQPRIME NGS Tumor Profiling Assay (FFPE) (GS6005)
1
Total
1
Cleared
0
Denied
Geneseeq Technology, Inc. has 1 FDA 510(k) cleared medical devices. Based in Toronto, CA.
Latest FDA clearance: Aug 2025. Active since 2025. Primary specialty: Pathology.
Browse the FDA 510(k) cleared devices submitted by Geneseeq Technology, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Geneseeq Technology, Inc.
1 devices