Vericom Co., Ltd.

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

Vericom Co., Ltd. has submitted 19 FDA 510(k) premarket notifications since 2004, of which 19 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Material, Impression, Material, Tooth Shade, Resin, Resin, Root Canal Filling, Sealant, Pit And Fissure, And Conditioner, Varnish, Cavity . Use the specialty filter in the sidebar to narrow results.