Isolux America

Isolux America — FDA 510(k) Submissions

Isolux America has submitted 3 FDA 510(k) premarket notifications since 1999, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laparoscope, Gynecologic (and Accessories), Illuminator, Fiberoptic, Surgical Field, Light, Surgical, Fiberoptic . Use the specialty filter in the sidebar to narrow results.