JD Supra

Key Takeaways from the AI Trends in Medical Devices Panel at the 2025 FDLI Annual Conference

Ariel Seeley served on the panel titled AI Trends in Medical Devices: Global Developments, FDA Policies, and Software as a Medical Device at the 2025 Food and Drug Law Institute (FDLI) Annual ...
Medscape

Panel Agrees Spinal Sphere Devices Need Premarket Approval

Given the lack of information on their effectiveness and the unreasonable risks for illness or injury, spinal sphere devices should be regulated as Class 3 devices that require premarket approval (PMA ...
MD&M East

FDA Panel Snubs J&J Heart Implant

A 15-person FDA Circulatory System Devices Panel has unanimously voted against Johnson & Johnson MedTech’s V-Wave Ventura interatrial shunt, creating a setback for the major medtech leader. The panel ...
Chicago Sun-Times

FDA panel reviewing Abbott heart device included 10 doctors with financial ties to the north suburban health giant

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Healio

FDA panel recommends TriClip TEER device for severe tricuspid regurgitation

Please provide your email address to receive an email when new articles are posted on . An FDA panel voted that the benefits of a transcatheter edge-to-edge repair device outweigh risks in severe ...
MedPage Today

FDA Panel Mulls Which Devices Are Critical in a Public Health Emergency

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Healio

FDA panel says risks of radiofrequency renal denervation device outweigh benefits

Please provide your email address to receive an email when new articles are posted on . An FDA panel voted that for adults with uncontrolled hypertension, the benefits of a radiofrequency renal ...