Whip-Mix Corp.

Whip-Mix Corp. — FDA 510(k) Submissions

Whip-Mix Corp. has submitted 6 FDA 510(k) premarket notifications since 2008, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Abutment, Implant, Dental, Endosseous, Resin, Denture, Relining, Repairing, Rebasing, Powder, Porcelain, Agent, Polishing, Abrasive, Oral Cavity . Use the specialty filter in the sidebar to narrow results.