Vesiflo, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vesiflo, Inc. - FDA 510(k) Cleared Devices
1
Total
0
Cleared
1
Denied
Vesiflo, Inc. has 0 FDA 510(k) cleared medical devices. Based in Redmond, US.
Active since 2014. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Vesiflo, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vesiflo, Inc.
1 devices