Isolux, LLC is one of 18949 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Isolux, LLC - FDA 510(k) Cleared Devices
Recent clearances: OptiLux LED Illuminator, ISOLED AC-POWERED LED HEADLIGHT SYSTEM, 1125 XSB XENON FIBER-OPTIC LIGHT SOURCE
3
Total
3
Cleared
0
Denied
Isolux, LLC has 3 FDA 510(k) cleared medical devices. Based in Naples, US.
Historical record: 3 cleared submissions from 2005 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Isolux, LLC Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Intertek Testing Services and Third Party Review Group, LLC.
FDA 510(k) Regulatory Record - Isolux, LLC
3 devices