Theravant Corporation is one of 5692 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Theravant Corporation - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Theravant Corporation has 2 FDA 510(k) cleared medical devices. Based in Cary, US.
Historical record: 2 cleared submissions from 2010 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Theravant Corporation Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Theravant Corporation
2 devices