Medexel Co.,Ltd

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

Medexel Co.,Ltd has submitted 3 FDA 510(k) premarket notifications since 2016, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Needle, Hypodermic, Single Lumen, Low Dead Space Piston Syringe . Use the specialty filter in the sidebar to narrow results.