Nvision Biomedical Technologies, Inc.

Nvision Biomedical Technologies, Inc. — FDA 510(k) Submissions

Nvision Biomedical Technologies, Inc. has submitted 22 FDA 510(k) premarket notifications since 2019, of which 22 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Screw, Fixation, Bone, Bone Wedge, Plate, Fixation, Bone, Intervertebral Fusion Device With Bone Graft, Lumbar, Intervertebral Fusion Device With Bone Graft, Cervical . Use the specialty filter in the sidebar to narrow results.