SONOMOTION ANNOUNCES FDA DE NOVO CLEARANCE FOR ITS STONE CLEAR™ DEVICE

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SonoMotion, Inc.

Nov 13, 2024, 09:34 ET

  • First and only device using non-invasive ultrasound pulses to facilitate passage of kidney stone fragments post-lithotripsy
  • Kidney stones affect one in 10 people in the US, costing $10 billion annually1

SAN MATEO, Calif., Nov. 13, 2024 /PRNewswire/ -- SonoMotion, a medical device company developing non-invasive solutions for kidney stones, announced today that the FDA has granted de novo clearance for the Company's Stone Clear™ device for the anesthesia-free treatment of post-lithotripsy kidney stone fragments. Stone Clear is the first and only device that delivers ultrasound pulses externally to move and facilitate the passage of residual fragments without surgery and in the clinic setting.

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SonoMotion's Stone Clear is the first and only FDA-cleared device using non-invasive ultrasound pulses to facilitate passage of kidney stone fragments post-lithotripsy without surgery and in any health care setting.
SonoMotion's Stone Clear is the first and only FDA-cleared device using non-invasive ultrasound pulses to facilitate passage of kidney stone fragments post-lithotripsy without surgery and in any health care setting.

"Patients with post-lithotripsy residual fragments are more likely to have complications, emergency department visits, or repeat procedures, yet they have no reliable non-invasive option aside from passive observation," said James E. Lingeman, MD, Clinical Professor of Urology, Indiana University School of Medicine. "The Stone Clear device provides patients with a non-invasive option to reduce their residual fragment stone burden in the clinic environment while being fully awake."

The Stone Clear device is part of a platform designed to treat kidney stones without requiring anesthesia and in any health care settings where a patient with a kidney stone may present themselves, including the doctor's office and emergency departments. Ultrasound propulsion in patients with post-lithotripsy residual fragments reduced the risk of relapse by 70% compared to standard-of-care observation.2 Results from the randomized controlled clinical trial with up to five-year follow-up are published in the December 2024 issue of the Journal of Urology.

SonoMotion's second solution, called Break Wave™, will operate on the same platform and will use focused ultrasound to non-invasively fragment kidney stones in the upper urinary tract without anesthesia and in a clinic setting. Break Wave is currently undergoing clinical trials in the United States and Canada. 

"SonoMotion's goal is to fundamentally change how kidney stones are treated, and securing FDA clearance for Stone Clear is a major milestone towards this goal," commented Oren Levy, PhD, Co-Founder and Chief Executive Officer, SonoMotion. "SonoMotion's technologies have the potential to be a first-line treatment for kidney stones, offering a solution for patients who want to avoid anesthesia, minimize wait times for surgery without the need for urinary stenting – a procedure often more painful than the kidney stone itself."

ABOUT SONOMOTION
SonoMotion, a VC-backed startup based in San Mateo, CA, is a clinical stage medical technology company developing next generation non-invasive solutions for the treatment of kidney stones. The SonoMotion Break Wave device is an investigational device that is not approved for sale in the U.S. or anywhere in the world. To learn more, please visit www.sonomotion.com.

References:

  1. Litwin MS, CS S. NIH Publication No. 12-7865.
  2. Sorensen MD et al. Randomized Controlled Trial of Ultrasonic Propulsion–Facilitated Clearance of Residual Kidney Stone Fragments vs Observation. Journal of Urology. 2024 Dec 1;212(6):811–20.

SOURCE SonoMotion, Inc.

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