Unilene Sac is one of 5205 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Unilene Sac - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Unilene Sac has 2 FDA 510(k) cleared medical devices. Based in Greenwood Village, US.
Historical record: 2 cleared submissions from 2010 to 2013. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Unilene Sac Filter by specialty or product code using the sidebar.
Unilene Sac — FDA 510(k) Products and Clearance History
2 devices
Cleared
May 28, 2013
VITAL SUTURES SUTUREX CIRUGIA PERUANA SUTUMED
General & Plastic Surgery
242d
Cleared
Dec 14, 2010
VITAL SUTURES, SUTUREX, CIRUGIA PERUANA
General & Plastic Surgery
270d