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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• Acrylic Bone Cement

• Anterior Old Plating Systems

• 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

• 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.

• Bio Absorbable Plating Systems

• Bioabsorbable synthetic spacers

• Bioreabsorbable Bone Cement

• Bone Cement (FDA Code: LOD / 888.3027)

• Bone Fixation Screw (FDA Code: HWC / 888.3040) A smooth or threaded metallic bone fixation fastener is a device intended to be implanted that consists of a stiff wire segment or rod made of alloys, such as cobalt-chromium-molybdenum and stainless steel, and that may be smooth on the outside, fully or partially threaded, straight or U-shaped; and may be either blunt pointed, sharp pointed, or have a formed, slotted head on the end. It may be used for fixation of bone fractures, for bone reconstructions, as a guide pin for insertion of other implants, or it may be implanted through the skin so that a pulling force (traction) may be applied to the skeletal system.

• Brushite Bone Cement

• Calcium Phosphate Bone Cements

• Canal Occluder

• Cannulated Interference Screws

• Cement Restrictor Hip Prosthesis (FDA Code: JDK / 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.

• Cervical Total Disc Replacement

• Fluid Management Systems

• Hand Operating Table

• Hand Tables

• Hip Replacement Instrumentation Kit

• Hip Replacement, Femoral Heads

• Humeral Nailing System

• Interference Screws

• Lavage Systems

• Low Viscosity Bone Cements

• Lumbar Total Disc Replacement

• Metal Cemented Femoral Component Hip Prosthesis (FDA Code: JDG / 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.

• Metal-on-Metal Hip System

• Metal/Polymer Femoral Hemi- Hip Prosthesis (FDA Code: KWY / 888.3390) A hip joint femoral (hemi-hip) metal/polymer cemented or uncemented prosthesis is a two-part device intended to be implanted to replace the head and neck of the femur. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a snap-fit acetabular component made of an alloy, such as cobalt-chromium-molybdenum, and ultra-high molecular weight polyethylene. This generic type of device may be fixed to the bone with bone cement (888.3027) or implanted by impaction.

• Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: LPH / 888.3358) A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a device intended to be implanted to replace a hip 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 has a femoral component made of a cobalt-chromium-molybdenum (Co-Cr-Mo) alloy or a titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high molecular weight polyethylene articulating bearing surface fixed in a metal shell made of Co-Cr-Mo or Ti-6Al-4V. The femoral stem and acetabular shell have a porous coating made of, in the case of Co-Cr-Mo substrates, beads of the same alloy, and in the case of Ti-6Al-4V substrates, fibers of commercially pure titanium or Ti-6Al-4V alloy. 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. The generic type of device has a design to achieve biological fixation to bone without the use of bone cement.

• Multiple Component Fixation Appliance (FDA Code: KTT / 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.

• Old Plating Systems

• Operating Room Equipment, Fluid Management Systems

• Orbital Procedures, Titanium Plating Systems

• Orthopedic Radial Head implant

• Pedicle Screw System

• Plating Systems

• Polyaxial Pedicular Screw System

• Posterior

• Posterior Cervical Plating Systems

• posterior cruciate ligament Instruments

• Pre Filled Bone Cement Mixer

• Pulsed Lavage System

• Radial Head Implants

• Removable synthetic spacers

• Semi-Constrained Acetabular Hip Prosthesis (FDA Code: KWA / 888.3330) A hip joint metal/metal semi-constrained, with an uncemented acetabular component, prosthesis is a two-part device intended to be implanted to replace a hip 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 consist of a femoral and an acetabular component, both made of alloys, such as cobalt-chromium-molybdenum. The femoral component is intended to be fixed with bone cement. The acetabular component is intended for use without bone cement (888.3027).

• Semi-Constrained Patellofemorotibial Knee Prosthesis (FDA Code: JWH / 888.3560) A knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a knee 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 a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components and a retropatellar resurfacing component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those prostheses intended for use with bone cement (888.3027).

• Sensory Prosthesis

• Simplex Tobramycin Bone Cement

• Solo Pulsed Lavage System