Cook Biotech, Incorporated
Contact: Mr. Mark Bleyer - President & CEO
Web: http://www.cookbiotech.com
E-Mail:
Address: 1425 Innovation Place, West Lafayette, Indiana 47906, USA
Phone: +1-(765)-497-3355, 888-299-4224 | Map/Directions >>
Profile: Cook Biotech, Incorporated is a developer and manufacturer of tissue grafts utilizing extracellular matrix technology. We offer regenerative medicine and products designed specifically to repair or reinforce weak or damaged tissue. The products are used in hernia repair, fistula repair, plastic surgery, staple line reinforcement, continence restoration, Peyronie's disease, dural repair and pelvic floor repair. We provide dural graft, Dynamatrix™ oral graft, SiS ophthalmic, and Oasis® wound matrix for head & neck parts. The Oasis wound matrix is a biologically derived extracellular matrix-based wound product that is compatible with human tissue. It is indicated for use in all partial and full thickness wounds & skin loss injuries, as well as superficial and second-degree burns. We also offer products for torso, abdomen, pelvis, arms and hands, & feet and legs.
The company was founded in 1995, has ~50 employees and is ISO 9001, CE certified.
FDA Registration Number: 1835959
25 Products/Services (Click for related suppliers)
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| • Abdominal Lock Grafts |
| • Anterior Pelvic Floor Graft |
| • Collagen Wound Dressing (FDA Code: KGN) |
| • Dura-Substitute (FDA Code: GXQ / 882.5910) A dura substitute is a sheet or material that is used to repair the dura mater (the membrane surrounding the brain). |
| • Dural Grafts |
| • Female External Urethral Occluder (FDA Code: MNG / 876.5160) A urological clamp for males is a device used to close the urethra of a male to control urinary incontinence or to hold anesthetic or radiography contrast media in the urethra temporarily. It is an external clamp. |
| • Fistula Plugs |
| • Hernia Repair Grafts |
| • Hiatal Hernia Grafts |
| • Inguinal Hernia Grafts |
| • Nerve Connectors |
| • Nerve Cuff (FDA Code: JXI / 882.5275) A nerve cuff is a tubular silicone rubber sheath used to encase a nerve for aid in repairing the nerve (e.g., to prevent ingrowth of scar tissue) and for capping the end of the nerve to prevent the formation of neuroma (tumors). |
| • Ophthalmic Devices |
| • Oral Grafts |
| • Pericardial Closures |
| • Polymeric Surgical Mesh (FDA Code: FTL / 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. |
| • Polypropylene PTFE PETP Pledget and Intracardiac Patch (FDA Code: DXZ / 870.3470) An intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene is a fabric device placed in the heart that is used to repair septal defects, for patch grafting, to repair tissue, and to buttress sutures. |
| • Posterior Pelvic Floor Graft |
| • Surgical Mesh (FDA Code: FTM / 878.3300) |
| • Tension-Free Urethral Slings |
| • Tissue Graft (FDA Code: LXA) |
| • Ulnar Nerve Protector |
| • Umbilical Hernia Grafts |
| • Urethral Sling |
| • Vaginal Erosion Repair Grafts |
