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SANUWAVE Health to Present at the Sixth Annual Noble Financial Equity Conference on June 7, 2010


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ALPHARETTA, Ga.--([ BUSINESS WIRE ])--SANUWAVE Health, Inc., (OTCBB: SNWV) ([ www.sanuwave.com ]), an emerging medical technology company focused on regenerative medicine, will participate in the Sixth Annual Noble Financial Equity Conference taking place June 7-8, 2010 at the Seminole Hard Rock Hotel in Hollywood, Florida.

Christopher M. Cashman, President and CEO of SANUWAVE, will present a corporate update on Monday, June 7, 2010 at 9:30 a.m. ET in which he will discuss an overview of SANUWAVE, including its Investigational Device Exemption (IDE) clinical trial for the treatment of diabetic foot ulcers that completed patient enrollment in the first quarter of 2010, as well as its strategic initiatives in the wound care, orthopedic and aesthetic market segments. The Phase III IDE clinical trial is evaluating Pulsed Acoustic Cellular Expression (aPACEa"a) technology and the safety and efficacy of the Companya™s lead product, dermaPACEa", in healing diabetic foot ulcers compared to standard of care.

Company management will be available for one-on-one meetings with investors participating in the Noble Financial Equity Conference. For those who would like to schedule an appointment with SANUWAVEa™s management, please contact Anne Marie Fields, Lippert/Heilshorn & Associates, Inc., at 212-838-3777 or at [ afields@lhai.com ] or contact your Noble Financial representative.

The presentation will be webcast live at [ http://www.sanuwave.com/investors/investorevents.html ] where it will also be archived for 90 days.

About SANUWAVE Health, Inc.

SANUWAVE Health, Inc. ([ www.sanuwave.com ]) is an emerging regenerative medicine company focused on the development and commercialization of non-invasive, biological response activating devices for the repair and regeneration of tissue, musculoskeletal and vascular structures. SANUWAVEa™s portfolio of products and product candidates activate biologic signaling and angiogenic responses, including new vascularization and microcirculatory improvement, helping to restore the bodya™s normal healing processes and regeneration. SANUWAVE intends to apply its Pulsed Acoustic Cellular Expression (PACEa") technology in wound healing, orthopedic/spine, plastic/cosmetic and cardiac conditions. Its lead product candidate for the global wound care market, dermaPACEa", is CE marked for treatment of the skin and subcutaneous soft tissue and is currently involved in an FDA-approved Investigational Device Exemption trial in the U.S. for the treatment of diabetic foot ulcers. SANUWAVE researches, designs, manufactures, markets and services its products worldwide and believes it has already demonstrated that this technology is safe and effective in stimulating healing in chronic conditions of the foot (plantar fasciitis) and the elbow (lateral epicondylitis) through its U.S. Class III PMA approved Ossatron® device, as well as stimulating bone and chronic tendonitis regeneration in the musculoskeletal environment through the utilization of its Ossatron® and Evotrona" devices in Europe.

Safe Harbor Statement

This press release may contain aforward-looking statementsa within the meaning of the Private Securities Litigation Reform Act of 1995, such as statements relating to financial results and plans for future business development activities, and are thus prospective. Forward-looking statements include all statements that are not statements of historical fact regarding intent, belief or current expectations of the Company, its directors or its officers.Investors are cautioned that any such forward-looking statements are not guarantees of future performance and involve risks and uncertainties, many of which are beyond the Companya™s ability to control.Actual results may differ materially from those projected in the forward-looking statements.Among the key risks, assumptions and factors that may affect operating results, performance and financial condition are risks associated with the marketing of the Companya™s product candidates and products, unproven pre-clinical and clinical development activities, regulatory oversight, the Companya™s ability to manage its capital resource issues, competition, and the other factors discussed in detail in the Companya™s periodic filings with the Securities and Exchange Commission.The Company undertakes no obligation to update any forward-looking statement.


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