Vygon USA

Vygon USA — FDA 510(k) Submissions

Vygon USA has submitted 4 FDA 510(k) premarket notifications since 2018, of which 4 received clearance as substantially equivalent to a predicate device.

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