The Clearant Process® has the ability to sterilize bone while not affecting the osteoinductive and osteoconductive nature of the allograft. The Clearant Process® is an extensively researched methodology with numerous tests completed measuring efficacy. Studies show radiation performed within the optimized conditions of the Clearant Process® maintains impresive allograft strength. The Clearant Process® is compatible with lyophilized shelf stable bone and frozen bone and bone-tendon allografts. Click here to see a list of our products.

Rigorous testing every step of the way

Mechanical and biological testing in the laboratory along with clinical experience have demonstrated the safety and efficacy of Clearant Process® allografts. The Clearant Process® has been successfully applied to and tested on cancellous wedges, cortical-cancellous wedges, human bone powder, crushed cancellous, crushed cortical, human DBM, and cortical bone rings and struts.

Tissue treated with the Clearant Processs®...

• Ensures the sterility level of at least a medical device while protecting biomechanical integrity.
• Inactivates a wide range of bacteria and viruses, including robust inactivation of West Nile Virus, HIV, Hepatitis A and Hepatitis C.
• Preserves stuctural and functional integrity and biologic activity.
• Increases safety assurance as the only terminal process applied to tissue products in the final sterile barrier packaging ready for the operating-room

Osteointegration

Tissue treated with the Clearant Process® effectively heals and integrates well with surrounding tissue. Independent studies, analyzing spinal fusion and calvarial defect models, have successfully demonstrated fusion. (Journal references and reprints available by contacting Clearant).

Clearant Process® radiated tissues maintain stability under stress.

Scoring of Bone Incorporation and Regeneration