Encore Medical, L.P.

Encore Medical, L.P. — FDA 510(k) Submissions

Encore Medical, L.P. has submitted 81 FDA 510(k) premarket notifications since 2002, of which 81 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Shoulder Prosthesis, Reverse Configuration, Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer, Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented, Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented, Prosthesis, Hip, Semi-constrained (metal Uncemented Acetabular Component) . Use the specialty filter in the sidebar to narrow results.