Belport Company, Inc., Gingi-Pak

Belport Company, Inc., Gingi-Pak — FDA 510(k) Submissions

Belport Company, Inc., Gingi-Pak has submitted 10 FDA 510(k) premarket notifications since 2020, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cord, Retraction, Varnish, Cavity, Mouthguard, Prescription, Resin, Denture, Relining, Repairing, Rebasing, Diammine Silver Fluoride Dental Hypersensitivity Varnish . Use the specialty filter in the sidebar to narrow results.