Zest Anchors, Inc.

Zest Anchors, Inc. — FDA 510(k) Submissions

Zest Anchors, Inc. has submitted 14 FDA 510(k) premarket notifications since 1980, of which 14 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Implant, Endosseous, Root-form, Abutment, Implant, Dental, Endosseous, Attachment, Precision, All, Splint, Endodontic Stabilizing . Use the specialty filter in the sidebar to narrow results.