AZmed Secures FDA 510(k) Clearance for Rayvolve in Pediatric Fracture Detection Through Study with SimonMed Imaging, Expanding Its AI-Powered Medical Imaging Solutions

PARIS, Sept. 3, 2024 /PRNewswire/ — European MedTech startup AZmed, recognized as a leading company in AI for medical imaging, today announced that its Rayvolve solution has received 510(k) clearance from the Food and Drug Administration (FDA) for detecting fractures on pediatric X-rays. This milestone comes two years after receiving FDA clearance for adult fracture detection, positioning Rayvolve as a top-performing solution for detecting fractures in adult and pediatric patients. The clearance was supported by an independent study conducted with SimonMed Imaging, one of the largest outpatient imaging providers in the U.S.

“The 510(k) clearance reflects our commitment to meeting the needs of healthcare professionals,” said Julien VIDAL, CEO of AZmed. “We are excited to extend our innovation to pediatric care, empowering clinicians with advanced tools to achieve the best outcomes for their patients.”

Through rigorous bench testing, the study with SimonMed Imaging confirmed Rayvolve’s efficacy in clinical settings, further validating AZmed’s commitment to collaborating with healthcare leaders to advance medical imaging technology. Involving a dataset of 3,000 pediatric radiographs, the study demonstrated Rayvolve’s high sensitivity (96%) and specificity (86%), making it one of the most effective software for assisting radiologists in detecting fractures in children, with an Area Under the Curve (AUC) of 94%.

“We are proud to have contributed to validating Rayvolve’s effectiveness,” said Dr. Sean Raj, Chief Innovation Officer of SimonMed Imaging. “This study underscores the transformative potential of AI as an indispensable diagnostic tool for pediatric fracture detection.”

For AZmed, obtaining FDA clearance opens a growth opportunity in the U.S. medical imaging market. The plan to introduce Rayvolve to more U.S. healthcare professionals aims to enhance traditional methods by focusing on quicker fracture detection and reducing the impact of fatigue and workload on clinicians. As Rayvolve gains traction, AZmed remains focused on developing AI-driven, clinically validated innovations that improve patient care and operational efficiency.

About AZmed:

Founded in 2018, AZmed is a European MedTech startup committed to revolutionizing medical imaging through AI-powered solutions. Its flagship product, Rayvolve, enhances X-ray diagnostics, improving accuracy and saving valuable time for healthcare professionals. Rayvolve, both FDA-cleared and CE-marked, streamlines radiology workflows by prioritizing critical cases and expediting treatment planning. Used by more than 2,000 healthcare facilities worldwide, Rayvolve transforms patient care and operational efficiency in medical imaging. For more information, visit azmed.co.

Logo – https://healthtechnologynet.com/wp-content/uploads/2024/09/AZmed_Logo.jpg

Contact:
Moshank Relia
moshank@azmed.co 

View original content:https://www.prnewswire.com/news-releases/azmed-secures-fda-510k-clearance-for-rayvolve-in-pediatric-fracture-detection-through-study-with-simonmed-imaging-expanding-its-ai-powered-medical-imaging-solutions-302236044.html

SOURCE AZmed

Staff

Recent Posts

Summit of Whose Future? Girls Have the Answers: Leaders Must Listen

Young Women Activists Launch "What Girls Want," Demand World Leaders Put Girls at the Center…

18 hours ago

Smart for Life Provides Update Following Nasdaq Delisting Due to Audit Delays; Reports Plans to Reapply to Nasdaq Upon Full Compliance

MIAMI, Sept. 20, 2024 (GLOBE NEWSWIRE) -- Smart for Life, Inc. (OTC: SMFL) (“Smart for…

21 hours ago

Global Ultrasound Institute Launches GUSI Fellowships Platform: Elevating Point-of-Care Ultrasound Education

SAN FRANCISCO, Sept. 20, 2024 /PRNewswire/ -- The Global Ultrasound Institute (GUSI) is proud to…

1 day ago