Vesocclude Medical, LLC is one of 4827 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vesocclude Medical, LLC - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Vesocclude Medical, LLC has 2 FDA 510(k) cleared medical devices. Based in Spring Hope, US.
Historical record: 2 cleared submissions from 2009 to 2016. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Vesocclude Medical, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vesocclude Medical, LLC
2 devices