Penumbra, Inc. announced the results of the THUNDER investigational device exemption (IDE) study evaluating the safety and ...
Spryte Medical announced the completion of patient enrollment of the INSYTE trial of the company’s investigational neuro OCT ...
Fujifilm Sonosite, Inc., a developer of point-of-care ultrasound (POCUS) solutions, announced the launch of Sonosite iLook, its co ...
Arsenal Medical announced late-breaking results from the EMBO-02 first-in-human (FIH) clinical study, which is evaluating the ...
Fluidx Medical Technology, Inc. announced results from a pivotal clinical trial evaluating the company’s GPX embolic device.
Imperative Care announced the launch of the Ikon 24 Pro guidewire. The next-generation neurovascular guidewire is designed ...
Rapid Medical announced FDA clearance of its Drivewire 35, which is a steerable 0.035-inch guidewire designed to help physicians r ...
HistoSonics announced that it has received approval in Europe for its Edison system, enabling the commercialization of the ...
The Society for Cardiovascular Angiography and Interventions (SCAI) announced that a multisociety expert consensus statement ...
FDA approves a 76-mm version of Abbott’s Esprit BTK resorbable scaffold system for patients with CLTI. The longer scaffold is intended to reduce the number of devices needed to treat long BTK lesions ...
Xeltis announced the official start of the European commercialization of aXess vascular access device for patients requiring hemod ...
Stereotaxis announced that it has completed its previously announced acquisition of Robocath, a Rouen, France-based developer ...
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