SUWANEE, GA--(Marketwired - Jun 8, 2017) - SANUWAVE Health, Inc. (OTCQB: SNWV) is pleased to announce that
the company is entering into a Memorandum of Understanding with eKare, Inc. to develop novel wound care analysis and management
solutions. Linking SANUWAVE's dermaPACE® wound treatment device with eKare's inSight® 3D wound imaging
and analytics system, the two companies will strive to produce the industry's most comprehensive wound management solution.
inSight uses the latest computer vision and 3D sensing technology to quickly and accurately assess the healing progress of
wounds and feed that data into its AI (Artificial Intelligence) analytics engine to drive actionable insights. inSight is
registered as a 510(k) Class I device and is CE Marked. SANUWAVE has long recognized that wound closure is but the end result of
a series of evolving treatment decisions, made more complicated by a diabetic patient population. Leveraging eKare's AI
analytic platform, SANUWAVE will develop proprietary clinical decision support system for the dermaPACE solution to improve the
outcome and lower the cost of wound care.
States Kevin Richardson, CEO of SANUWAVE, "Having conducted and analyzed two highly controlled wound studies, we
have recognized that successful wound closure is dependent upon recognizing and adapting to multiple factors in a patient's
overall medical situation to effectively close wounds as quickly as possible. With eKare's inSight, SANUWAVE believes that
we have found the perfect platform for clinicians to manage the chess match that is wound closure." Adds Travis Smith, Chief
Commercial Officer of eKare, "We are excited to be teaming with SANUWAVE to elevate inSight's strength in imaging and analytics
to develop better treatment algorithms for the dermaPace solution. This potent combination of therapy, 3D imaging, and data
analytics can pave the path to powerful and cost effective wound closure solutions."
SANUWAVE dermaPACE, CE Marked and licensed in Canada, Australia, and South Korea has a proven record of effectiveness in
treating skin conditions, particularly diabetic foot ulcers and venous leg ulcers. In the US, SANUWAVE has completed two US
based clinical trials enrolling 336 subjects, which have proven the dermaPACE to be safe and effective in the treatment of
Diabetic Foot Ulcers. Within a few weeks of initial treatment, wounds treated with dermaPACE reduce in area at superior
rates compared to control subjects. dermaPACE exhibits superiority in wound area reduction within 12 weeks of initial
treatment and exhibits superiority in wound closure within 20 weeks of initial treatment. Combined with the imaging and
analytical power of inSight, the two companies intend to jump to the forefront in intelligent wound management and healing.
SANUWAVE intends to introduce the inSight system into additional clinical trials planned for 2017.
For more information on SANUWAVE's technology, please read our blog, "Shock This", on our website at www.sanuwave.com. Additional information for eKare can be found on their website at www.ekareinc.com.
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.
About eKare, Inc.
eKare Inc. (http://ekare.ai) is dedicated to the design and
development of wound assessment solutions using the latest machine intelligence, computer-vision, and mobile technology. eKare's
current technology offering include wound tissue classification, mobile 3D imaging, as well as AI analytics engine to draw
clinical insights and business intelligence. eKare's innovative technology is creating new possibilities in how we deliver wound
care across the healthcare continuum, from inpatient hospital and skilled nursing facilities to ambulatory clinics and
telemedicine.
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 .