Profile: Corin Group PLC develops orthopaedic products. Our product line comprises of hip systems, knee systems, upper limb, sports injury and spinal products. Our rotaglide+ total knee system gives the surgeon complete flexibility in matching a proven knee replacement to the specific needs of individual patients. Our trinity polyaxial screw system provides better performance and ease of use for the orthopaedic surgeon. The Oxford Shoulder™ has been designed so that the prosthesis replaces the humeral head and glenoid as anatomically as possible. Our Zenith TAR system is an unconstrained, mobile bearing, titanium alloy device with a cementless BONIT® coating for enhanced fixation.

The company has revenues of USD 25-50 Million, has ~140 employees and is ISO 9001, CE certified.

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• Spinal Interlaminal Fixation Appliance (FDA Code: KWP / 888.3050) A spinal interlaminal fixation orthosis is a device intended to be implanted made of an alloy, such as stainless steel, that consists of various hooks and a posteriorly placed compression or distraction rod. The device is implanted, usually across three adjacent vertebrae, to straighten and immobilize the spine to allow bone grafts to unite and fuse the vertebrae together. The device is used primarily in the treatment of scoliosis (a lateral curvature of the spine), but it also may be used in the treatment of fracture or dislocation of the spine, grades 3 and 4 of spondylolisthesis (a dislocation of the spinal column), and lower back syndrome.

• Spinal Intervertebral Body Fixation Appliance (FDA Code: KWQ / 888.3060) A spinal intervertebral body fixation orthosis is a device intended to be implanted made of titanium. It consists of various vertebral plates that are punched into each of a series of vertebral bodies. An eye-type screw is inserted in a hole in the center of each of the plates. A braided cable is threaded through each eye-type screw. The cable is tightened with a tension device and it is fastened or crimped at each eye-type screw. The device is used to apply force to a series of vertebrae to correct "sway back," scoliosis (lateral curvature of the spine), or other conditions.

• Spinal Products

• Synthetic Spacers

• Taper-Fit Hip System

• Total Disc Replacements

• Total Knee Prosthesis

• Traditional Bone Cements

• 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.

• vacuum Bone Cement Mixing Systems