Since the 2017 publication of the medical device regulation (MDR) and the IVD regulation (IVDR), EU regulations for medical ...
The FDA announced that it removed a limitation on the use of real-world evidence (RWE) in drug and device application reviews ...
St. Paul medical device companies Minnetronix Medical and Intricon recently merged to form a new contract design and ...
The FDA recently had a meeting to explore regulatory aspects of AI-enabled mental health medical devices. I explore a useful ...
Patent strengthens Company's global intellectual property portfolio and reinforces the Company's commitment to establishing ...
GlobalData on MSN
FDA clears CMR Surgical’s Versius Plus robot
CMR Surgical has secured US Food and Drug Administration (FDA) clearance for its Versius Plus minimally invasive robotic ...
Finding the right vagus nerve stimulation device can be tricky; TPIMS reviewed dozens and found the most effective options ...
Armstrong Asia of Singapore selected as NeuroSigma’s manufacturing partnerInvestment led by Checkmate Capital as part of ...
CMR Surgical said it is on track to begin commercialization of its Versius Plus surgical robotic platform in 2026 in the ...
Scientific and Medical Equipment House Co. (Equipment House) signed today, Dec. 16, an exclusive distribution agreement with ...
Comparative trials are among the hardest studies to execute in medtech, especially when the control arm is a long-established standard of care. Arun Menawat, CEO of Profound Medical, understands how ...
CMR Surgical announced today that its second-generation surgical robot, Versius Plus, received FDA 510(k) clearance.
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