Liaoning Upcera Co., Ltd.

Liaoning Upcera Co., Ltd. — FDA 510(k) Submissions

Liaoning Upcera Co., Ltd. has submitted 10 FDA 510(k) premarket notifications since 2014, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Powder, Porcelain, Crown And Bridge, Temporary, Resin, Material, Tooth Shade, Resin, Agent, Tooth Bonding, Resin . Use the specialty filter in the sidebar to narrow results.