GE HealthCare Technologies Inc. GEHC recently announced that it has obtained FDA 510(k) clearance and CE Marking for its ...

Cynosure Lutronic has announced CE Mark approval under the European Medical Device Regulation (MDR) for its Mosaic 3D ...

HighLife announced today that it received CE mark approval for its transcatheter mitral valve replacement (TMVR) system.

First-and-only test of its kind approved under new European Union regulations expands access to personalized cancer care for patients across the EU This in vitro diagnostic (IVD) assay, which has been ...

Medtronic announced two new milestones for its Affera Sphere-360 catheter for pulsed field ablation (PFA) procedures.

HighLife Receives CE Mark Approval for its TMVR SolutionParis, January 26, 2026 – HighLife SAS, a leading MedTech company focused on ...

PCOS affects between 10% and 13% of women worldwide. Image credit: Toey Andante via Shutterstock.com. France-headquartered May Health has secured a European CE mark for its Anavi system to address ...

PARIS & SAN FRANCISCO--(BUSINESS WIRE)--Moon Surgical, a French-American pioneer in collaborative robotics, announced today that the latest version of its Maestro System is CE Marked under the Medical ...

After the West Bengal catheter scam, Rajasthan has ordered a recall of CE-marked neonatal catheters over quality lapses, ...

As previously announced, the UK government has enacted legislation to continue the recognition of the CE marking indefinitely for a range of products falling within the scope of 21 regulations, ...