Kenota, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Kenota, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Kenota 1 Total IgE
1
Total
1
Cleared
0
Denied
Kenota, Inc. has 1 FDA 510(k) cleared medical devices. Based in Kitchener, CA.
Latest FDA clearance: May 2024. Active since 2024. Primary specialty: Immunology.
Browse the FDA 510(k) cleared devices submitted by Kenota, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Kenota, Inc.
1 devices