Theravant Corporation is one of 5263 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.
Theravant Corporation — FDA 510(k) Products and Clearance History
2 devices
Cleared
Mar 04, 2013
ACLEARA, THERACLEAR
General & Plastic Surgery
76d
Cleared
Jul 08, 2010
THERACLEAR
General & Plastic Surgery
49d