Vygon USA is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vygon USA - FDA 510(k) Cleared Devices
Recent clearances: Nutrifit, Leaderflex Mini and Leaderflex Nano, Vygon Midline 3 Fr SL Catheter
4
Total
4
Cleared
0
Denied
Vygon USA has 4 FDA 510(k) cleared medical devices. Based in Lansdale, US.
Latest FDA clearance: Dec 2024. Active since 2018. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Vygon USA Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vygon USA
4 devices