New MHRA PMS requirements hit UK medtech industry
The new regulation tightens safety and performance monitoring rules for all medical devices placed on the UK market after 16 June 2025.
Qiagen and Incyte to develop diagnostic panel for myeloproliferative neoplasms
InspireMD’s embolic prevention system gains CE Mark approval
FDA tags Medtronic鈥檚 voluntary ventilator recall as Class I after patient death
New synthetic skin improves robots’ ability to sense touch
FDA grants 510(k) clearance to Viz.ai鈥檚 Viz Subdural Plus module
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Themes
View MoreNeuralink secures $650m in Series E to advance brain implant technology
The company's trials are underway at neurosurgical care institutions across three countries.
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Data Insights
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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