Cynosure Lutronic has announced CE Mark approval under the European Medical Device Regulation (MDR) for its Mosaic 3D ...
GE HealthCare (Nasdaq: GEHC) announced today that it received FDA 510(k) clearance and CE mark for its Allia Moveo platform.
Abbott received Europe’s CE mark for a dual-ablation catheter used to treat a common heart arrhythmia, the company said ...
Zacks Investment Research on MSN
SENS stock up as Eversense 365 CGM wins European CE mark approval
Senseonics Holdings, Inc. SENS recently scored a meaningful regulatory win in Europe, receiving CE Mark approval for its ...
HighLife Receives CE Mark Approval for its TMVR SolutionParis, January 26, 2026 – HighLife SAS, a leading MedTech company focused on ...
Medical Device Network on MSN
Abbott secures CE mark for Tactiflex dual ablation catheter
TactiFlex Duo builds on Abbott’s electrophysiology portfolio with a catheter than can ablate irregular heart rhythms using ...
Medtronic announced two new milestones for its Affera Sphere-360 catheter for pulsed field ablation (PFA) procedures.
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 ...
Rockfield Medical Devices Limited Receives CE Mark Approval for the Mobility+® Enteral Feeding System, Marking a Major Milestone in Global Commercial Expansion ...
Highlife SAS secured CE mark for its transcatheter mitral valve replacement (TMVR) system, bringing a much needed treatment ...
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