Ide Vision, Ltd.

Ide Vision, Ltd. — FDA 510(k) Submissions

Ide Vision, Ltd. has submitted 1 FDA 510(k) premarket notifications since 2024, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Insufflator, Automatic Carbon-dioxide For Endoscope . Use the specialty filter in the sidebar to narrow results.