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Suneva Medical Announces Corporate Developments Including Appointment of Philip Ranker as Chief Financial Officer
Date:12/4/2009

nd strategic planning expertise, coupled with his history of delivering results in his previous roles, will no doubt enhance Suneva's Aesthetic Market growth objectives."

Additional Suneva Medical Corporate Developments:

  • Artefill® Market Roll-Out: Since May 2009, Suneva Medical has been actively re-engaging an exclusive group of dermatologists, plastic surgeons and aesthetic physicians about the long-lasting benefits and value of Artefill, the only FDA-approved microsphere-enhanced collagen dermal filler. The response has been overwhelmingly positive as patients continue to seek a filler that will provide long-term wrinkle correction for the nasolabial folds (the lines from the end of the nose to the corners of the mouth). As of December 2009, 20,000+ patients have been successfully treated with Artefill and the numbers continue to grow under the leadership of Suneva Medical and due to the rapid adoption of the technology by skilled physician injectors.
  • California State FDA Establishment Inspection: In August 2009, the California State FDA, Food and Drug Branch, determined that Suneva Medical had met the cGMP requirements for a medical device company to legally manufacture and distribute product. Following successful completion of its California State FDA Establishment Inspection and the ISO 13485:2003 Inspections, Suneva Medical began manufacturing and distributing Artefill at its California-based manufacturing facility.
  • Long-Term Safety and Patient Satisfaction Clinical Trial: A prospective 5-year study of 1,008 Artefill® patients is currently being conducted to examine the long-term safety and patient satisfaction of Artefill. This trial is currently the largest filler safety trial conducted to-date and the longest-term, longitudinal filler safety trial ever conducted in the U.S. Thus far, the safety results of Artefill have met our expectations
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SOURCE Suneva Medical
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