Anthogyr

Anthogyr — FDA 510(k) Submissions

Anthogyr has submitted 10 FDA 510(k) premarket notifications since 2004, of which 10 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Sterilization Wrap Containers, Trays, Cassettes & Other Accessories, Handpiece, Belt And/or Gear Driven, Dental, Handpiece, Direct Drive, Ac-powered, Implant, Endosseous, Root-form, Abutment, Implant, Dental, Endosseous . Use the specialty filter in the sidebar to narrow results.