Kleinostheim, Germany, 10th February 2011 - curasan
AG, which is listed in the General Standard of the German Stock
Exchange (ISIN: DE 000 549 453 8), has received FDA certification and,
therefore, marketing authorization throughout the USA of the synthetic
bone replacement material Osbone® Dental which already has been authorized in the EU as Osbone®.
Dental is suitable for utilisation in general bone surgery,
particularly in implantology and oral and maxillofacial surgery
associated with jawbone atrophy.
product consists of an open-celled, porous and biocompatible
hydroxylapatite ceramic. It is extremely well tolerated by tissue, is
not absorbable and is firmer than standard bone substance, which
complies with the wishes of many physicians and dentists. Its spongy,
interconnected cells match the natural bone trabecula structure, thereby allow integration into the surrounding viable bone. As a pure synthetic product Osbone®
Dental has no biological origins, therefore, it is not associated with
any risks relating to potential infections or the development of
Background information about curasan AG:
listed curasan AG (ISIN: DE 000 549 453 8) is one of the leading firms
in the field of regenerative medicine especially in bone and tissue
regeneration. In addition to the synthetic Cerasorb® bone
substitution and regeneration material, the company has developed a
future-oriented product pipeline, which will be ready for market rollout
within the next few years via well-positioned contractual partners in
various market segments.
Tel. +49 (0)6027 40 900-51
Fax +49 (0)6027 40 900-39
fr financial relations gmbh
Tel. +49 (0)69 95 90 83 20
Fax +49 (0)69 95 90 83 99
Last Updated on Sunday, 06 March 2011 13:23
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