Thermi is one of 4730 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thermi - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Thermi has 2 FDA 510(k) cleared medical devices. Based in Irving, US.
Historical record: 2 cleared submissions from 2016 to 2017. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Thermi Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Thermi
2 devices