University Spin-out Awarded Compliance Mark

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University Spin-out Awarded Compliance Mark

22 Feb, 2019

Published over 7 years ago. See the latest and most current information on News.

In a development that represents new hope for repairing challenging bone fractures, a University of Aberdeen spinout has received a CE mark for a synthetic bone graft substitute. SIRAKOSS Ltd has announced it has been granted CE Mark clearance in the European Union (EU) for Osteo3, the nanosynthetic bone graft substitute designed to improve patient healing. This new technology has been designed to provide patients with more complete healing as well as allowing less time under anaesthesia, when it is launched into hospitals.

SIRAKOSS, spun out in 2011, is a developer of synthetic bone graft substitutes that are designed to transform the treatment of spinal fusions and bone defects. Based on proprietary nanoporous technology, Osteo3 consists of an inorganic matrix that is completely reabsorbed into the bone. Osteo3 has a unique surface chemistry designed to catalyse rapid and complete bone regeneration following a fracture or to support the skeletal system after corrective surgery of a degenerative or deformity condition. SIRAKOSS is developing further generations of Osteo3 to facilitate intraoperative ease of use by surgeons.

“Osteo3 is the first of our new generation of bone substitute products to receive CE Mark, a major milestone for SIRAKOSS. We believe our approach could provide the definitive synthetic bone graft product and feedback from surgeons on performance has been very encouraging,” said Tom Buckland, Director of SIRAKOSS. “The positive results in studies achieved to date suggests that Osteo3 is a potential game-changer in the synthetic bone graft substitute market, providing significant advantages to patients and surgeons, including in the most challenging bone fracture indications. SIRAKOSS’ priority is executing on its commitment to delivering robust clinical data demonstrating safety and effectiveness of this exciting new product.”

Under its CE Mark, Osteo3 is intended to be used as a bone graft material for filling voids or gaps of the skeletal system. Osteo3 can be used alone or in combination with autograft, the patient’s own bone, or allograft (donor tissue).

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