Enchant Tek Co. , Ltd.

Enchant Tek Co. , Ltd. — FDA 510(k) Submissions

Enchant Tek Co. , Ltd. has submitted 2 FDA 510(k) premarket notifications since 2024, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Spirometer, Therapeutic (incentive), Nebulizer (direct Patient Interface) . Use the specialty filter in the sidebar to narrow results.