Interpore Cross International, Inc.

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Web: http://www.crossmedical.com
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Address: 181 Technology Drive, Irvine, California 92618, USA
Phone: +1-(949)-453-3200 | Fax: +1-(949)-453-3225 | Map/Directions >>

Profile: Interpore Cross International, Inc. is a public medical device company, which focuses on products for spinal surgery. Our CDO system renders key benefits for surgeons and their patients, including diagnostic capabilities, better control of material delivery, significantly reduced procedural times & shorter recovery time. Our geo allows radiographic visualization of the graft site postoperatively for better assessment of fusion. Our InterGro DBM products combine the osteoinductivity of DBM with a natural, non-soluble carrier that won't wash away, delivering a unique bone graft that offers handling and performance characteristics & can be easily formed to fit any shape fracture or defect. our Pro Osteon resorbable bone graft material is derived from an abundant non-decorative coral. It is available in a selection of fully resorbable sterile granules and blocks, in a variety of shapes and sizes.

The company was founded in 1975, has revenues of USD 50-100 Million, has ~150 employees and is ISO 9001, CE certified. NASDAQ:BONZ (SEC Filings)

FDA Registration Number: 2029012

38 Products/Services (Click for related suppliers)

• Allograft Bone Graft

• Artificial Hydroxyapatite

• Artificial Hydroxyapatite Orbital Implant

• Autologous Platelet Gel Preparation Systems

• Bio-Eyes Hydroxyapatite Orbital Implant

• Bioabsorbable synthetic spacers

• Bone Graft Harvester

• Bone Graft Impactor

• Bone Graft Regeneration Fixation Kit

• Bone Graft Replacement

• Bone Graft Screw System

• Bone Graft Substitute Blocks

• Bone Graft Substitute Osteotomy Wedges

• Bone Graft Substitute Plugs

• Bone Grafting Forceps

• Bone grafting Osteotomes

• Bone Grafting Syringe

• Bone Grafting Wheel

• Calcium Compound Bone Void Filler (FDA Code: MQV / 888.3045)

A resorbable calcium salt bone void filler device is a resorbable implant intended to fill bony voids or gaps of the extremities, spine, and pelvis that are caused by trauma or surgery and are not intrinsic to the stability of the bony structure.

• 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.

• Demineralized Bone Matrix

• Enteral Irrigation Kit w/Piston Syringe

• Hollow Fiber Capillary Dialyzer (FDA Code: FJI / 876.5820)

A hemodialysis system and accessories is a device that is used as an artificial kidney system for the treatment of patients with renal failure or toxemic conditions and that consists of an extracorporeal blood system, a conventional dialyzer, a dialysate delivery system, and accessories. Blood from a patient flows through the tubing of the extracorporeal blood system and accessories to the blood compartment of the dialyzer, then returns through further tubing of the extracorporeal blood system to the patient. The dialyzer has two compartments that are separated by a semipermeable membrane. While the blood is in the blood compartment, undesirable substances in the blood pass through the semipermeable membrane into the dialysate in the dialysate compartment. The dialysate delivery system controls and monitors the dialysate circulating through the dialysate compartment of the dialyzer.

• Human Demineralized Bone Matrix

• Hydroxyapatite

• Hydroxyapatite Coated Implants

• Hydroxyapatite Orbital Implants

• Methyl Methacrylate for Cranioplasty (FDA Code: GXP / 882.5300)

Methyl methacrylate for cranioplasty (skull repair) is a self-curing acrylic that a surgeon uses to repair a skull defect in a patient. At the time of surgery, the surgeon initiates polymerization of the material and forms it into a plate or other appropriate shape to repair the defect.

• Osteoinduction Bone Void Filler (FDA Code: MBP / 888.3045)

• Osteoinductive Demineralized Bone Matrix

• Patellofemorotibial Knee Prosthesis (FDA Code: MBH / 888.3565)

A knee joint patellofemorotibial metal/polymer porous-coated uncemented 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 is designed to achieve biological fixation to bone without the use of bone cement. This identification includes fixed-bearing knee prostheses where the ultra high molecular weight polyethylene tibial bearing is rigidly secured to the metal tibial base plate.

• Piston Syringe (FDA Code: FMF / 880.5860)

A piston syringe is a device intended for medical purposes that consists of a calibrated hollow barrel and a movable plunger. At one end of the barrel there is a male connector (nozzle) for fitting the female connector (hub) of a hypodermic single lumen needle. The device is used to inject fluids into, or withdraw fluids from, the body.

• Porous hydroxyapatite orbital implants

• Removable synthetic spacers

• Stopcock, I.V.Set (FDA Code: FMG / 880.5440)

An intravascular administration set is a device used to administer fluids from a container to a patient's vascular system through a needle or catheter inserted into a vein. The device may include the needle or catheter, tubing, a flow regulator, a drip chamber, an infusion line filter, an I.V. set stopcock, fluid delivery tubing, connectors between parts of the set, a side tube with a cap to serve as an injection site, and a hollow spike to penetrate and connect the tubing to an I.V. bag or other infusion fluid container.

• Synthetic Bone Graft

• Synthetic Bone Graft Substitute Granules

• Synthetic Spacers