Medical Device Manufacturer · CA , Milton

Keter Canada, Inc. - FDA 510(k) Cleared Devices

1 submissions · 1 cleared · Since 2025
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.
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