Vygon Corporation

Vygon Corporation — FDA 510(k) Submissions

Vygon Corporation has submitted 1 FDA 510(k) premarket notifications since 2025, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Catheter, Intravascular, Therapeutic, Long-term Greater Than 30 Days . Use the specialty filter in the sidebar to narrow results.