Unilene Sac is one of 19064 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Unilene Sac - FDA 510(k) Cleared Devices
Recent clearances: VITAL SUTURES SUTUREX CIRUGIA PERUANA SUTUMED, VITAL SUTURES, SUTUREX, CIRUGIA PERUANA
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.
FDA 510(k) Regulatory Record - Unilene Sac
2 devices