[Sonic Incytes] FDA Grants 510(k) Clearance for Sonic Incytes’ Velacur ONE™, AI-Guided Point of Care
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[Sonic Incytes]

VANCOUVER, British Columbia--(BUSINESS WIRE)--Sonic Incytes Medical Corp, proudly announces that the U.S. Food and Drug Administration (FDA) has granted 510(k) clearance for Velacur ONE™, its point-of-care ultrasound elastography device. Building on the success of its original model, Velacur™, Velacur ONE™ introduces an enhanced interface and features for improved portability and user experience. These improvements enable broader scalability to support Sonic Incytes’ accelerated US and global expansion strategy. Velacur ONE™ measures attenuation, VDFF (Velacur Determined-Fat Fraction), and liver stiffness using 3D S-WAVE and aids in the management of chronic liver disease including MASH and MASLD.
Velacur ONE™ arrives at a critical time for
improved non-invasive testing, following the recent FDA clearance of Rezdiffra—the
first therapeutic for Metabolic dysfunction–associated steatohepatitis (MASH),
a progressive and often underdiagnosed liver disease. In the U.S. alone, an
estimated 100 million adults have Metabolic dysfunction–associated Steatotic
Liver Disease (MASLD)1, with 15–20 million of those affected by MASH2. Yet, 90%
of MASH cases remain undiagnosed3. If left untreated, worsening MASH increases
morbidity and may progress to severe complications, including cirrhosis, liver
failure, liver cancer, and liver transplant4,5. MASH remains challenging to
diagnose effectively due to the limitations of existing non-invasive methods,
especially those available at the point-of-care.
With the first therapeutic now available
and more in the pipeline, clinicians need improved non-invasive tests to
diagnose and monitor MASH at point-of-care6. Current treatment guidelines for
MASH recommend imaging-based elastography, such as Velacur™, to assess liver
scarring (fibrosis) and fat content (steatosis). While ultrasound elastography
is widely used, when it comes to treating patients with MASH, liver stiffness
alone cannot be relied on to assess treatment response in the short term7. The best
predictor of treatment responses was a decrease in steatosis (identified as ≥30%
reduction in MRI-PDFF)8.
VDFF, Sonic Incytes’ proprietary algorithm
that received FDA clearance in 2024, demonstrates a strong correlation (r =
0.85) with MRI-PDFF—the gold standard for liver fat measurement—and achieves an
outstanding accuracy (AUC) of 95% of patients with more than 5% MRI-PDFF,
defining the presence of hepatic steatosis9. Velacur ONE™ combines this
technology with a refined user interface, including B-mode imaging—enabling 3–4x
higher reimbursement than non-imaging elastography—and an AI-based organ
overlay feature to aid in liver localization, making it the only point-of-care
device that estimates both liver stiffness and attenuation that correlates to
MRI-PDFF10.
“The launch of Velacur ONE™ marks a pivotal
milestone for Sonic Incytes as we accelerate our US and global commercial
expansion strategy,” said Barry Allen, CEO of Sonic Incytes. “This
next-generation device enhances clinical utility and operational scalability,
positioning us to better support the growing demand for accessible,
non-invasive liver diagnostics and treatment, particularly in the management of
MASLD and MASH at the point-of-care.”
Sonic Incytes is committed to enhancing
patient care through innovative diagnostic solutions. The company’s flagship
product, Velacur™, equips physicians with an advanced liver imaging tool to
help manage the growing epidemic of fatty liver disease. Velacur™ offers
real-time, AI-guided quantification of the key markers for fatty liver disease:
liver stiffness, attenuation and VDFF. With real-time results, a low up-front
cost and AI guidance, Velacur™ makes liver imaging at the point-of-care
affordable and accessible.