Keter Canada, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Keter Canada, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Community Containers (Flap and Daisy)
1
Total
1
Cleared
0
Denied
Keter Canada, Inc. has 1 FDA 510(k) cleared medical devices. Based in Milton, CA.
Latest FDA clearance: Oct 2025. Active since 2025. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Keter Canada, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by The FDA Group as regulatory consultant.
FDA 510(k) Regulatory Record - Keter Canada, Inc.
1 devices