News
ClearNote Health has commenced subject enrolment in a multicentre, prospective study involving its Avantect pancreatic cancer ...
Corvia Medical has raised $55m to complete an ongoing clinical trial of its atrial shunt system for heart failure.
Health Canada has granted approval for Abbott’s i-STAT TBI test cartridge, aiding clinicians in evaluating suspected ...
New regulations from the UK’s MHRA around post-market surveillance (PMS) requirements for medical devices have come into ...
The Society of Thoracic Surgeons (STS) in the US has introduced a mobile application, the STS Risk Calculator App.
Italy-based Bracco Imaging and Subtle Medical have obtained an EU CE mark for AiMIFY, a jointly developed software designed ...
Qiagen, Incyte have announced a master collaboration agreement to create a diagnostic panel to aid in the treatment of ...
InspireMD’s CGuard Prime Embolic Prevention System (EPS) has secured CE Mark approval under the European MDR for stroke ...
This breakthrough shows that a robot’s outer skin can be reshaped, reused and remain functional - critical in human-robot ...
Medtronic has announced a voluntary recall of select Newport HT70 and Newport HT70 Plus ventilators and certain related service parts.
The US Food and Drug Administration (FDA) has granted 510(k) clearance to Viz.ai for its Viz Subdural Plus module.
Presidio Medical has received an IDE approval from the FDA, enabling a pivotal study of its neuromodulation platform.
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