
Sonio receives FDA 510(k) clearance for Sonio Detect
We are thrilled to share that our revolutionary AI-powered solution, Sonio Detect, has received FDA 510(k) clearance.

We are thrilled to share that our revolutionary AI-powered solution, Sonio Detect, has received FDA 510(k) clearance.
We are thrilled to share that our revolutionary AI-powered solution, Sonio Detect, has received FDA 510(k) clearance.
Sonio Detect is a Software as a Service SaaS solution. It aims at helping sonographers, OB/GYNs, MFMs, and Fetal surgeons to perform their routine fetal ultrasound examinations in real time. Sonio Detect leverages deep learning networks to assist ultrasound practitioners in ensuring better Quality, Efficiency, and Expertise throughout the entire exam in real-time by automatically:
Sonio Detect is one of the very few AI solutions for OBGYNs, MFMs, Sonographers and Clinical Experts that can integrate with various ultrasound manufacturers. It is verified to have high sensitivity and specificity and maintain this high accuracy across various subgroups of patients (including BMI, maternal age, and ethnicity).
The FDA's recognition represents a groundbreaking milestone in our mission to revolutionize maternal care on a global scale.
As we move forward, fueled by this remarkable achievement, we remain committed to pushing the boundaries of medical technology.
Our AI-augmented ultrasounds offer a comprehensive window into the health and development of their unborn child. This technology-driven experience provides a deeper connection and understanding, alleviating anxieties and offering a clearer picture of the journey ahead. With the FDA's stamp of clearance, we're not only advancing maternal care but also marking the beginning of a transformative journey in the USA.
Sonio Detect is part of Sonio, the next-generation of Prenatal Ultrasounds.
