Nearly a third of FDA medical device adverse event reports filed late
A new study found that 9.1% of medical device AEs were reported to the FDA 180 days later than required over a three-year period.
FDA grants 510(k) clearance for J&J MedTech’s Monarch Quest
Vivani Medical to spin-off neurostim business Cortigent as public company
Renal denervation: An advanced procedure to relieve hypertension
FDA approves GT Metabolic Solutions’ 50mm magnet in MagDI System
Australia’s TGA approves Body Vision’s AI imaging system
Analysis
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View MoreNHS ups AI push with Cera software rollout for fall prediction
Cera’s platform is also being deployed to detect winter illnesses amongst community health services.
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View MoreArtificial intelligence: who are the leaders in histology image analysis software for the medical devices industry?
The medical devices industry continues to be a hotbed of patent innovation. Activity is driven by increased need for homecare,...
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Apple UK update transforms AirPods into hearing aids
Scientists develop largest ever biological AI model that ‘thinks in nucleotides’
Why 2025 is a key year for the surgical robotics market
GenAI clinical conversation startup Abridge scoops $250m