Cryolife Inc.

Address: 1655 Roberts Blvd NW, Kennesaw, Georgia 30144, USA
Phone: +1-(770)-419-3355, 800-438-8285 | Fax: +1-(770)-426-0031 | Map/Directions >>

Profile: CryoLife® Inc. is a biomedical company that produces low temperature preservation of human tissues for implant. Our CryoLife-O'Brien® stentless aortic porcine valve is made of three non-coronary leaflets & is implanted with a single suture line technique. Our BioGlue® surgical adhesive is a two-component surgical adhesive composed of purified bovine serum albumin (BSA) and glutaraldehyde. Our HemoStase™ is a natural hemostatic product used for the control of surgical bleeding. It is a plant-based powder that rapidly dehydrates blood and promotes clotting on contact by controlling the clotting factors. Our BioGlue&surgical adhesive is used in cardiovascular surgery. It begins to polymerize within 20 to 30 seconds and reaches its bonding strength within two minutes. It also adheres to synthetic graft materials through mechanical bonding within the interstices of the graft matrix.

The company was founded in 1984, has revenues of USD 50-100 Million, has ~400 employees and is ISO 9001, CE certified. NYSE:CRY (SEC Filings)

FDA Registration Number: 1063481

30 Products/Services (Click for related suppliers)  
• Allografts
• Aortic Valve
• Aortic Valve Allograft
• BioGluer Syringe
• Biological Arterial Graft
• Biological Cardiac Valve Prosthesis (FDA Code: DYE / 870.3925)
A replacement heart valve is a device intended to perform the function of any of the heart's natural valves. This device includes valves constructed of prosthetic materials, biologic valves (e.g., porcine valves), or valves constructed of a combination of prosthetic and biologic materials.
• Cardiac Valve Prosthesis
• Collagen Tendon Prosthesis
• Collagen-Based Non-Absorbable Hemostatic Agent (FDA Code: LMG / 878.4490)
An absorbable hemostatic agent or dressing is a device intended to produce hemostasis by accelerating the clotting process of blood. It is absorbable.
• Heart Valve Allograft (FDA Code: MIE)
• Heart-Valve, Non-Allograft Tissue (FDA Code: LWR)
• Ligament Prosthesis (FDA Code: HWF)
• Mechanical Heart Valve (FDA Code: LWQ)
• More Than Minimally Manipulated Allograft Heart Valve (FDA Code: OHA)
• Passive Closure Devices, Femoral artery
• Patch Materials for Cardiac Valve Replacement
• Pericardial Sheet
• 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.
• Pulmonary Artery Branch Patch Material
• Pulmonary Valve Allograft
• Pulmonary Valves for Cardiac Valve Replacement
• Small Diameter Vascular Graft Prosthesis (FDA Code: DYF / 870.3450)
A vascular graft prosthesis is an implanted device intended to repair, replace, or bypass sections of native or artificial vessels, excluding coronary or cerebral vasculature, and to provide vascular access. It is commonly constructed of materials such as polyethylene terephthalate and polytetrafluoroethylene, and it may be coated with a biological coating, such as albumin or collagen, or a synthetic coating, such as silicone. The graft structure itself is not made of materials of animal origin, including human umbilical cords.
• surgical adhesive
• Surgical Glue For Arteries (FDA Code: MUQ)
• Surgical Mesh (FDA Code: FTM / 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.
• Surgical Sealants
• Surgical Tissue Glue
• Tendon Prosthesis Implant
• Tissue Graft (FDA Code: LXA)
• Vascular Graft Prosthesis (FDA Code: DSY / 870.3450)

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