Isolux, LLC is one of 4741 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Isolux, LLC - FDA 510(k) Cleared Devices
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.
FDA 510(k) Regulatory Record - Isolux, LLC
3 devices