La Lumiere, LLC is one of 5625 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
La Lumiere, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
La Lumiere, LLC has 2 FDA 510(k) cleared medical devices. Based in Austin, US.
Historical record: 2 cleared submissions from 2013 to 2015. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by La Lumiere, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - La Lumiere, LLC
2 devices