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

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

The UPC has granted a preliminary injunction effective for Germany, France, Italy, the Netherlands and Ireland against a Chinese medical device manufacturer and its Dutch subsidiary over the ...

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 ...

The Mosaic 3D device incorporates several features designed to enhance safety and patient comfort.

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, ...

HighLife plans to prioritise procedural consistency and imaging-guided follow-up for safety in early commercial settings.

SAINT-FERRÉOL-D'AUROURE, France, Jan. 07, 2026 (GLOBE NEWSWIRE) -- Hexadrone SAS announces that it has obtained CE marking as well as C5 and C6 class certifications for its TUNDRA 2.1 drone. The ...

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--(BUSINESS WIRE)--Regulatory News: CARMAT (FR0010907956, ALCAR), designer and developer of the world’s most advanced total artificial heart, aiming to provide a therapeutic alternative for ...

Rockfield Medical Devices Limited Receives CE Mark Approval for the Mobility+® Enteral Feeding System, Marking a Major Milestone in Global Commercial Expansion ...