Introducing RESONIC
Soliton, Inc. Rolls Out Its Rapid Acoustic Pulse
HOUSTON, May 5, 2021 /PRNewswire/ — Soliton, Inc., (Nasdaq: SOLY) (“Soliton” or the “Company”), a medical device company with a novel and proprietary aesthetic platform technology, today announced the launch of its highly anticipated Rapid Acoustic Pulse
“This is an exciting day for Soliton and the RESONIC brand,” shared Brad Hauser, President & CEO of Soliton. “It’s been a long time in the making and we’re excited to finally bring this innovative and efficacious solution to procedures that have had historically low patient satisfaction or required numerous treatment sessions to achieve expected results. Launching RESONIC with two unique indications has been a strategic goal of ours since receiving our first FDA clearance in 2019. This approach enables our HCP partners to drive multiple revenue streams among two different patient profiles with one device, positioning our partners for accelerated practice growth, and poising RESONIC to become a leading aesthetics brand,” added Hauser.
Leveraging its proprietary technology, the RESONIC device is designed to safely deliver rapid, high-pressure acoustic shockwaves at a rate of up to 100 pulses per second, resulting in the physical change of targeted cellular structures without creating cavitation or heating that could result in surrounding tissue damage. The Rapid Acoustic Pulse technology creates a new standard in tattoo removal when used as an accessory to a Q-Switched laser, to allow for multiple laser passes and up to 44% fading in a single session with tattoo removal in as few as 3 sessions. This innovative technology also safely and non-invasively physically changes fibrous septa bands beneath the skin that cause cellulite to deliver efficacious results in just one, 45–60-minute treatment with minimal discomfort and without downtime.
“RESONIC revolutionizes the industry’s approach to two notoriously challenging patient needs. The technology’s ability to physically change targeted cellular structures without breaking the skin is game changing,” shared Dr. Elizabeth Tanzi, Board Certified Dermatologist and member of Soliton’s Scientific Advisory Board. “Clinical trial results for both RESONIC procedures showed significant results with accelerated treatment timelines, which I believe will result in higher patient satisfaction and will minimize common barriers to entry that exist for tattoo removal and cellulite reduction.”
RESONIC is cleared by the U.S. Food and Drug Administration (FDA) as an accessory to the 1064 nm Q-Switched laser for black ink tattoo removal in Fitzpatrick Skin Type I-III patients and short-term improvement in the appearance of cellulite.
RESONIC for Tattoo and RESONIC for Cellulite will be available through a select network of physicians and medically supervised spas beginning in June 2021. Visit http://www.RESONIC.com/ for more information and to find a physician near you.
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About RESONIC
The RESONIC
To learn more and view important safety information, visit http://www.resonic.com/.
About Soliton, Inc.
Soliton, Inc. is a medical device company with a novel and proprietary platform technology licensed from The University of Texas on behalf of MD Anderson Cancer Center. The Company’s first FDA cleared commercial product, RESONIC
For more information about the Company, please visit http://www.soliton.com/.