Genomadix, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Genomadix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Genomadix Cube CYP2C19 System
1
Total
1
Cleared
0
Denied
Genomadix, Inc. has 1 FDA 510(k) cleared medical devices. Based in Kanata (Ottawa), CA.
Last cleared in 2023. Active since 2023. Primary specialty: Toxicology.
Browse the FDA 510(k) cleared devices submitted by Genomadix, Inc. Filter by specialty or product code using the sidebar.
1 device has linked clinical trial registered on ClinicalTrials.gov.
FDA 510(k) Regulatory Record - Genomadix, Inc.
1 devices