Restor3D, Inc.

Restor3D, Inc. — FDA 510(k) Submissions

Restor3D, Inc. has submitted 6 FDA 510(k) premarket notifications since 2021, of which 6 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented, Bone Wedge, Prosthesis, Toe, Hemi-, Phalangeal, Prosthesis, Ankle, Semi-constrained, Cemented, Metal/polymer, Ankle Fusion Cage . Use the specialty filter in the sidebar to narrow results.