SANUWAVE Health Issues a New "SHOCK THIS" Blog
SUWANEE, GA--(Marketwired - Aug 2, 2017) - SANUWAVE Health, Inc. (OTCQB: SNWV) announces a new
installment of their blog, SHOCK THIS on its website www.sanuwave.com.
Similar to the prior ones, this post is from SANUWAVE's head of Research and Development, Dr. Iulian Cioanta, and is titled
"Don't Judge a Medical Shock Wave by its Cover", which provides a comparison between focused and unfocused shock waves. The
goal of the blog is to allow a medium to help educate customers, patients, partners, and the public about the various initiatives
under way at SANUWAVE. The blog will also accept posts and comments (approved by SANUWAVE), which the Company views as
valuable to the SANUWAVE community. This is expected to be a constructive forum for users from around the globe. By
having a central location, SHOCK THIS, the Company can bring together in one setting various information that will be useful and
entertaining to the SANUWAVE community. Members of the SANUWAVE community are encouraged to interact and reach out with
thoughts and ideas, which will positively impact the SANUWAVE community as a whole. SANUWAVE Health, Inc. reserves the right
to edit or exclude comments it deems not positively impacting the experience or is not appropriate from legal and regulatory
perspectives.
About SANUWAVE Health, Inc.
SANUWAVE Health, Inc. (OTCQB: SNWV) (www.sanuwave.com) is a shock wave
technology company initially focused on the development and commercialization of patented noninvasive, biological response
activating devices for the repair and regeneration of skin, musculoskeletal tissue and vascular structures. SANUWAVE's portfolio
of regenerative medicine products and product candidates activate biologic signaling and angiogenic responses, producing new
vascularization and microcirculatory improvement, which helps restore the body's normal healing processes and regeneration.
SANUWAVE applies its patented PACE technology in wound healing, orthopedic/spine, plastic/cosmetic and cardiac conditions. Its
lead product candidate for the global wound care market, dermaPACE®, is CE Marked throughout Europe and has device license
approval for the treatment of the skin and subcutaneous soft tissue in Canada, Australia and New Zealand. In the U.S., dermaPACE
is currently under the FDA's de novo petition review process for the treatment of diabetic foot ulcers. SANUWAVE
researches, designs, manufactures, markets and services its products worldwide, and believes it has demonstrated that its
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, Evotron® and orthoPACE®
devices in Europe, Asia and Asia/Pacific. In addition, there are license/partnership opportunities for SANUWAVE's shock wave
technology for non-medical uses, including energy, water, food and industrial markets.
Forward-Looking Statements
This press release may contain "forward-looking statements" 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 Company'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 regulatory approval and marketing of the Company's product candidates and products, unproven pre-clinical and
clinical development activities, regulatory oversight, the Company's ability to manage its capital resource issues, competition,
and the other factors discussed in detail in the Company's periodic filings with the Securities and Exchange Commission. The
Company undertakes no obligation to update any forward-looking statement.
For additional information about the Company, visit www.sanuwave.com .