Implant Corp. of America

Implant Corp. of America — FDA 510(k) Submissions

Implant Corp. of America has submitted 3 FDA 510(k) premarket notifications since 1993, of which 3 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Endosseous, Root-form, Guide, Surgical, Instrument, Drill, Dental, Intraoral . Use the specialty filter in the sidebar to narrow results.