Coviden (Formerly Registered AS US Surgical, A Div is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Coviden (Formerly Registered AS US Surgical, A Div - FDA 510(k) Clear...
1
Total
1
Cleared
0
Denied
Coviden (Formerly Registered AS US Surgical, A Div has 1 FDA 510(k) cleared medical devices. Based in North Haven, US.
Historical record: 1 cleared submissions from 2011 to 2011. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Coviden (Formerly Registered AS US Surgical, A Div Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Coviden (Formerly Registered AS US Surgical, A Div
1 devices