Medical Device Manufacturer · CA , Laval

Klox Technlogies, Inc. - FDA 510(k) Cleared Devices

1 submissions · 0 cleared · Since 2021

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) cleared devices by Klox Technlogies, Inc.

1 devices

1-1 of 1

Not Cleared Dec 03, 2021

Klox Biophotonic LumiHeal System

DEN200005 · QPE

General & Plastic Surgery · 668d