Digital health companies DarioHealth Corp (NASDAQ: DRIO) and OneStep announced on Monday a strategic collaboration to integrate smartphone-based, clinical-grade fall risk assessment technology into Dario's multi-condition digital health platform. The partnership aims to deliver measurable return on investment for health plans by reducing falls and improving outcomes among high-risk populations, including those with obesity and Medicare Advantage members experiencing frailty and balance issues.
Under a signed Memorandum of Understanding, with a Master Services Agreement expected shortly, Dario will incorporate OneStep's FDA-listed motion analysis technology to provide proactive fall risk identification and education. The integration will enable at-risk users to access real-time insights that support fall prevention and reduce related healthcare costs.
Falls generate more than USD50bn annually in direct medical expenses in the US, according to the Centers for Disease Control and Prevention, with Medicare and Medicaid covering around 75% of the total. The US fall management market, valued at nearly USD200m in 2024, is projected to exceed USD300m by 2033, reflecting a compound annual growth rate of more than 5%.
DarioHealth provides a multi-condition platform for chronic disease management across diabetes, hypertension, weight management, musculoskeletal pain and behavioral health.
OneStep's smartphone-based gait analysis technology delivers clinical mobility insights to support fall prevention and remote patient monitoring.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval