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

251 to 282 of 282 Products/Services (Click for related suppliers)  Page: 1 2 3 4 5 [6]

• Tibial IM Nails

• Tibiocalcaneal Arthrodesis Nails

• Tie-On Surgical Masks

• Titanium Ankle Arthrodesis

• Titanium Cannulated Screws

• Titanium Internal fixation Systems

• Total Ankle Arthroplasty System

• Total Ankle Replacement Device

• Total Ankle Systems

• Total Disc Replacements

• Total Knee Systems

• Total Shoulder Arthroplasty

• Total Shoulder Systems

• Total Wrist Arthroplasty

• Tourniquet Machines

• Tourniquet machines and accessories

• Tourniquets

• Traditional Bone Cements

• Triple Arthrodesis

• Tubular Elastic Bandage Retainer

• Tubular Elastic Bandages & Nets

• Ultra-Soft Surgical Mask for Sensitive Skin Indicator Organism Testing

• Ultrasonic Bone Cement Remover

• Uncemented Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: LWJ / 888.3360) A hip joint femoral (hemi-hip) metallic cemented or uncemented prosthesis is a device intended to be implanted to replace a portion of the hip joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum. This generic type of device includes designs which are intended to be fixed to the bone with bone cement (888.3027) as well as designs which have large window-like holes in the stem of the device and which are intended for use without bone cement. However, in these latter designs, fixation of the device is not achieved by means of bone ingrowth.

• Uncemented Metal/Polymer Shoulder Prosthesis (FDA Code: MBF / 888.3670) A shoulder joint metal/polymer/metal nonconstrained or semi-constrained porous-coated uncemented prosthesis is a device intended to be implanted to replace a shoulder joint. The device limits movement in one or more planes. It has no linkage across-the-joint. This generic type of device includes prostheses that have a humeral component made of alloys such as cobalt-chromium-molybdenum (Co-Cr-Mo) and titanium-aluminum-vanadium (Ti-6Al-4V) alloys, and a glenoid resurfacing component made of ultra-high molecular weight polyethylene, or a combination of an articulating ultra-high molecular weight bearing surface fixed in a metal shell made of alloys such as Co-Cr-Mo and Ti-6Al-4V. The humeral component and glenoid backing have a porous coating made of, in the case of Co-Cr-Mo components, beads of the same alloy or commercially pure titanium powder, and in the case of Ti-6Al-4V components, beads or fibers of commercially pure titanium or Ti-6Al-4V alloy, or commercially pure titanium powder. The porous coating has a volume porosity between 30 and 70 percent, an average pore size between 100 and 1,000 microns, interconnecting porosity, and a porous coating thickness between 500 and 1,500 microns. This generic type of device is designed to achieve biological fixation to bone without the use of bone cement.

• Uncemented total wrist Arthroplasty

• Urology Surgical Drapes (FDA Code: KKX / 878.4370) A surgical drape and drape accessories is a device made of natural or synthetic materials intended to be used as a protective patient covering, such as to isolate a site of surgical incision from microbial and other contamination. The device includes a plastic wound protector that may adhere to the skin around a surgical incision or be placed in a wound to cover its exposed edges, and a latex drape with a self-retaining finger cot that is intended to allow repeated insertion of the surgeon's finger into the rectum during performance of a transurethral prostatectomy.

• vacuum Bone Cement Mixing Systems

• Video Arthroscopes

• Wide Angle Arthroscopes

• Wrist Implants Arthrodesis Hardware

• Wrist Implants, Total Wrist Arthroplasty