Vortek Surgical, LLC is one of 24545 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vortek Surgical, LLC - FDA 510(k) Cleared Devices
Recent clearances: ENDODRAPE(TM), ENDODRAPE
2
Total
2
Cleared
0
Denied
Vortek Surgical, LLC has 2 FDA 510(k) cleared medical devices. Based in Indianapolis, US.
Historical record: 2 cleared submissions from 2007 to 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Vortek Surgical, LLC Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Intertek Testing Services as regulatory consultant.
FDA 510(k) Regulatory Record - Vortek Surgical, LLC
2 devices