Johnson & Johnson Professionals, Inc.

Johnson & Johnson Professionals, Inc. — FDA 510(k) Submissions

Johnson & Johnson Professionals, Inc. has submitted 206 FDA 510(k) premarket notifications since 1976, of which 184 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Material, Tooth Shade, Resin, Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer, Prosthesis, Hip, Hemi-, Femoral, Metal/polymer, Cemented Or Uncemented, Prosthesis, Hip, Semi-constrained, Metal/polymer, Cemented, Strip, Adhesive, Closure, Skin . Use the specialty filter in the sidebar to narrow results.