Uvx, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Uvx, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Zener® (model ZEN-001-B1)
1
Total
1
Cleared
0
Denied
Uvx, Inc. has 1 FDA 510(k) cleared medical devices. Based in Vancouver, CA.
Latest FDA clearance: Sep 2025. Active since 2025. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Uvx, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Third Party Review Group, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Uvx, Inc.
1 devices