The Libre Duo systems are the first glucose-ketone monitors to reach the diabetes market.

With the ever-increasing stringency, time, and expense associated with FDA approval for medical devices, debate is sharpening in the medical devices industry over whether it is actually better ...

Sentante now intends to establish partnerships with hospitals and healthcare providers across Europe to integrate its ...

SINGAPORE, June 3, 2026 /PRNewswire/ -- Reach Surgical, the surgical solutions division of Genesis MedTech, has received CE Mark approval for SOUND REACHTM Swift, ultrasonic shears designed for open ...

The UKCA mark was introduced in the Great British (GB) market to replace the European CE mark following Brexit. Products which require a CE mark in the EU must comply with the UKCA marking regime if ...

Cornerstone Robotics announced today that it received CE mark approval for its Sentire endoscopic surgical robotic platform.

CE mark certification comes after Hong Kong-based Cornerstone Robotics raised $200 million in November to accelerate its ...

This article will examine market access outside the EU/EEA based on reliance and recognition. For countries outside the European Union (EU) and European Economic Area (EEA), regulatory reliance and ...

Please provide your email address to receive an email when new articles are posted on . The ViaLase laser received a CE mark for the treatment of adults with primary open-angle glaucoma, according to ...

PRINCETON, N.J. and PARIS., STENTYS, a medical technology company commercializing the world's first and only Self-Apposing® coronary stent, today announced that the Company’s Drug-Eluting stent ...

RESEARCH TRIANGLE PARK, N.C.--(BUSINESS WIRE)--TransEnterix, Inc. (NYSE American:TRXC), a medical device company that is digitizing the interface between the surgeon and the patient to improve ...