Eden Spine Vertebral Body Replacement Receives CE Mark Approval

Lake Mary, FL, December 17, 2010 --(PR.com)-- Eden Spine (www.EdenSpine.com), a Florida based Medical Devices organization announced today that the GIZA™was granted CE Mark approval.

“The GIZA™ is a new generation VBR, specifically designed to save valuable O.R. time and decrease the risk of subsidence,” says Mourad Ben Mokhtar head of Eden Spine’s research and developments efforts.

The technology is intended to replace and fuse a collapsed, damaged, or unstable vertebral body due to a tumor or a fracture. It is a reliable and intuitive system for one or two level fusions.

“With its CE Mark,” added Guillaume Viallaneix, CEO, “the GIZA™is available for international distribution. US market approval is expected during the half of 2011.”

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As a technology driven organization, Eden Spine LLC, a privately held spine company headquartered in Lake Mary, Florida, is positively impacting patient care and creating substantial value developing tomorrows’ spinal technologies and building a world class spine franchise, inclusive of a fiscally responsible sales & distribution network. The Eden Spine Group is commercially active in the United States, Europe, the Middle East and Latin America. The company possesses 5 proprietary technologies including three new-generation, motion preservation technologies; the WellDisc™ total disc replacement; the Perfx-2™ Dynamic Stabilization System, and the Wellex™ Interspinous Technology. Eden Spine currently distributes a range of FDA-cleared and CE Marked spine technologies in the US and internationally.