Profile: Depuy Orthopaedics, Inc. designs, manufactures and distributes orthopaedic devices & supplies including hip, knee, extremity, trauma, orthobiologics & operating room products.

The company was founded in 1895. NYSE:DPU (SEC Filings)

FDA Registration Number: 1818910

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• 3 Part Metal-Plastic-Metal Articulation Wrist Prosthesis (FDA Code: JWJ / 888.3800) A wrist joint metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a wrist joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have either a one-part radial component made of alloys, such as cobalt-chromium-molybdenum, with an ultra-high molecular weight polyethylene bearing surface, or a two-part radial component made of alloys and an ultra-high molecular weight polyethylene ball that is mounted on the radial component with a trunnion bearing. The metallic portion of the two-part radial component is inserted into the radius. These devices have a metacarpal component(s) made of alloys, such as cobalt-chromium-molybdenum. This generic type of device is limited to those prostheses intended for use with bone cement (888.3027).

• AC-Powered Motor Orthopedic Surgical Instrument (FDA Code: HWE / 878.4820) Surgical instrument motors and accessories are AC-powered, battery-powered, or air-powered devices intended for use during surgical procedures to provide power to operate various accessories or attachments to cut hard tissue or bone and soft tissue. Accessories or attachments may include a bur, chisel (osteotome), dermabrasion brush, dermatome, drill bit, hammerhead, pin driver, and saw blade.

• AC-Powered Portable Ward Use Suction Apparatus (FDA Code: JCX / 878.4780) A powered suction pump is a portable, AC-powered or compressed air-powered device intended to be used to remove infectious materials from wounds or fluids from a patient's airway or respiratory support system. The device may be used during surgery in the operating room or at the patient's bedside. The device may include a microbial filter.

• AC-Powered Surgical Instrument Motor (FDA Code: GEY / 878.4820)

• Acetabular Liners

• Acetabular Mesh Hip Prosthesis (FDA Code: JDJ / 878.3300) Surgical mesh is a metallic or polymeric screen intended to be implanted to reinforce soft tissue or bone where weakness exists. Examples of surgical mesh are metallic and polymeric mesh for hernia repair, and acetabular and cement restrictor mesh used during orthopedic surgery.

• Acrylic Bone Cement

• Adhesive Elastic Bandage Tape

• All Poly Liners

• Allografts

• Alumina Acetabular Liners

• Ankle Arthrodesis Nailing Systems

• Ankle Arthrodesis Systems

• Ankle Arthroscopy Drill Guides

• Ankle External Fixators

• Ankle Implants Ankle Arthrodesis Systems

• Ankle Surgical Instruments, Ankle Arthroscopy Drill Guide

• Anti-Fog Surgical Mask with Adhesive Tape

• Antibiotic Bone Cement (FDA Code: MBB / 888.3027) Polymethylmethacrylate (PMMA) bone cement is a device intended to be implanted that is made from methylmethacrylate, polymethylmethacrylate, esters of methacrylic acid, or copolymers containing polymethylmethacrylate and polystyrene. The device is intended for use in arthroplastic procedures of the hip, knee, and other joints for the fixation of polymer or metallic prosthetic implants to living bone.

• Antibiotic Impregnated Bone Cement

• Arthrodesis Hardware

• Arthrodesis Nails

• Arthroscopes (FDA Code: HRX / 888.1100) An arthroscope is an electrically powered endoscope intended to make visible the interior of a joint. The arthroscope and accessories also is intended to perform surgery within a joint.

• Arthroscopic Ankle Joint Distracter

• Arthroscopic Meniscal Repair Systems

• arthroscopic Suture Anchor

• Arthroscopy Drill Guide System

• Arthroscopy Instruments

• Arthroscopy Shaver Systems

• Arthroscopy Shoulder Instrument Set

• Artificial Disc Replacement

• Artificial Hydroxyapatite

• Artificial Hydroxyapatite Orbital Implant

• Artificial Intervertebral Disc Replacement

• Autoclavable Arthroscopes

• Autoclavable Small Joint Arthroscopes

• Autologous Platelet Gel Preparation Systems

• Barrier Reusable Surgical Gowns

• Biaxial Total Wrist Arthroplasty

• Bio-Eyes Hydroxyapatite Orbital Implant

• Bioabsorbable synthetic spacers

• Bioreabsorbable Bone Cement

• Bone Allografts

• Bone Cement (FDA Code: LOD / 888.3027)

• Bone Cement Mixing Systems

• Bone Cement Radiopacifier

• Bone Cement Removal Devices

• Bone Cement Restrictor

• Bone Fixation Nail (FDA Code: JDS / 888.3030) Single/multiple component metallic bone fixation appliances and accessories are devices intended to be implanted consisting of one or more metallic components and their metallic fasteners. The devices contain a plate, a nail/plate combination, or a blade/plate combination that are made of alloys, such as cobalt-chromium-molybdenum, stainless steel, and titanium, that are intended to be held in position with fasteners, such as screws and nails, or bolts, nuts, and washers. These devices are used for fixation of fractures of the proximal or distal end of long bones, such as intracapsular, intertrochanteric, intercervical, supracondylar, or condylar fractures of the femur; for fusion of a joint; or for surgical procedures that involve cutting a bone. The devices may be implanted or attached through the skin so that a pulling force (traction) may be applied to the skeletal system.

• Bone Fixation Plate (FDA Code: HRS / 888.3030)