Olympus Corporations of the Americas

Olympus Corporations of the Americas — FDA 510(k) Submissions

Olympus Corporations of the Americas 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 Endoscopic Video Imaging System/component, Gastroenterology-urology . Use the specialty filter in the sidebar to narrow results.