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Osteotech Receives 13485:2003 ISO Certification; Company Meets International Standards for Medical Device Manufacturing
Date:2/19/2009

EATONTOWN, N.J., Feb. 19 /PRNewswire-FirstCall/ -- Osteotech, Inc. (Nasdaq: OSTE), a leader in the emerging field of biologic products for regenerative healing, announced today that it has received ISO 13485:2003 certification for its quality management system. Osteotech received ISO certification for developing, manufacturing and marketing of biologic, biomaterial and device systems for musculoskeletal surgery and the processing of human bone and connective tissue for transplantation. Osteotech's wholly-owned subsidiaries, OST Developpement SA and TB OsteoCentre Bulgaria EAD previously received ISO 9001 certification, and OST also previously received ISO 13485:2003 certification, for their quality management systems.

"We are very pleased to announce that we have received ISO certification for our U.S. quality management system," said Sam Owusu-Akyaw, President and Chief Executive Officer of Osteotech. "The certification reinforces our commitment to maintaining a high quality processing facility and to ensuring the safety of those patients that utilize our products. Receiving the certification is an important milestone as we continue towards our goal to become a leader in regenerative and biologic healing."

Osteotech's facilities in Eatontown, New Jersey and Clermont-Ferrand, France are the processing sites for the Company's allograft tissue grafts utilized in its broad portfolio of therapy-driven products focused on promoting regenerative and biologic healing. To date, Osteotech has successfully processed more than four million tissue grafts worldwide. The Company's advanced technology platforms, all processed at its Eatontown facility, include Grafton(R) DBM and the Plexur(R) Biocomposite family of products as well as the DuraTech(TM) BioRegeneration Matrix, Osteotech's leading product based upon its proprietary human collagen
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SOURCE Osteotech, Inc.
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