Orthonovis, Inc.

Orthonovis, Inc. — FDA 510(k) Submissions

Orthonovis, Inc. has submitted 5 FDA 510(k) premarket notifications since 2022, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Plate, Fixation, Bone, Appliance, Fixation, Nail/blade/plate Combination, Multiple Component, Screw, Fixation, Bone . Use the specialty filter in the sidebar to narrow results.