Teleflex reports new findings from a study showing the efficacy of its Arrow chlorhexidine-impregnated central venous ...

Medtronic (NYSE: MDT) has issued an urgent field safety notice in Europe related to its Hugo robotic surgical system's ...

GE HealthCare launched a new version of its MIM Encore imaging software, marking its first combined release since acquiring ...

DermaSensor today announced the publication of two pivotal studies validating its device for skin cancer detection in primary ...

Neurent Medical announced that it received FDA 510(k) clearance for its next-generation Neuromark system for chronic rhinitis ...

Accelus received FDA 510(k) clearance for its FlareHawk Interbody Fusion System to be safely scanned under certain MRI ...

Aortyx announced today that it brought in $16 million (€13.8 million) to support its bioresorbable aortic patch technology.

Epiminder today announced results from a clinical trial of its implantable continuous electroencephalogram monitoring (iCEM) ...

Presidio Medical has received FDA investigational device exemption (IDE) for its ultra-low frequency (ULF) neuromodulation ...

The procedure was performed by Dr. Stan Thornton at Thomas Hospital, part of Infirmary Health in Fairhope, Alabama. The U.S.

Medtronic today announced that it issued a voluntary recall notification related to specific Newport ventilators and related ...

Volta Medical announced a labeling update for its Volta AF-Xplorer decision support system following the publication of ...