Guilin Refine Medical Instrument Co., Ltd.

Guilin Refine Medical Instrument Co., Ltd. — FDA 510(k) Submissions

Guilin Refine Medical Instrument Co., 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 Scaler, Ultrasonic, Unit, X-ray, Extraoral With Timer, Activator, Ultraviolet, For Polymerization . Use the specialty filter in the sidebar to narrow results.