Magentiq Eye, Ltd.

Magentiq Eye, Ltd. — FDA 510(k) Submissions

Magentiq Eye, Ltd. has submitted 3 FDA 510(k) premarket notifications since 2023, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Gastrointesinal Lesion Software Detection System . Use the specialty filter in the sidebar to narrow results.