Vygon is one of 4838 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vygon - FDA 510(k) Cleared Devices
2
Total
2
Cleared
0
Denied
Vygon has 2 FDA 510(k) cleared medical devices. Based in Lansdale Montgomery, US.
Historical record: 2 cleared submissions from 2014 to 2016. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Vygon Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vygon
2 devices