Mekics Co., Ltd.

Mekics Co., Ltd. — FDA 510(k) Submissions

Mekics Co., Ltd. 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 Ventilator, Continuous, Minimal Ventilatory Support, Facility Use . Use the specialty filter in the sidebar to narrow results.