Klox Technlogies, Inc. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Klox Technlogies, Inc. - FDA 510(k) Cleared Devices
1
Total
0
Cleared
1
Denied
Klox Technlogies, Inc. has 0 FDA 510(k) cleared medical devices. Based in Laval, CA.
Active since 2021. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Klox Technlogies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Klox Technlogies, Inc.
1 devices