Varian, a Siemens Healthineers (ETR:SHL) company, on Tuesday announced the European launch of IntelliBlate, a CE-marked microwave ablation solution for soft tissue tumour treatment.
IntelliBlate integrates with Siemens Healthineers' image-guided therapy technologies, allowing clinicians to plan, place, treat, monitor and confirm ablation in a single clinical environment.
The system offers precision-driven, minimally invasive treatment, featuring dual generators, real-time temperature monitoring via the Ximitry probe, and a compact, intuitive design for simplified workflow and faster setup.
IntelliBlate supports large, controlled spherical ablation zones, offering tailored treatment options for individual patient needs. The product builds on US FDA clearance received in 2024 and arrives in Europe amid growing clinical evidence supporting thermal ablation as a first-line option, as highlighted in the COLLISION phase 3 trial published in The Lancet Oncology.
Varian will introduce IntelliBlate to the European clinical community at CIRSE 2025, with hands-on demonstrations and training sessions.
DATROWAY receives US priority review for first-line metastatic triple negative breast cancer
Lupin launches Dasatinib tablets in US market
Natera submits Signatera CDx PMA to FDA for bladder cancer use
Pharming receives FDA complete response letter for paediatric Joenja application
Trace Biosciences' IND application for nerve-specific imaging agent approved by FDA
Frontage expands early phase clinical research capabilities across US and China
MicuRx Pharmaceuticals' IND application for MRX-5 cleared by FDA
FDA approves Tenpoint Therapeutics' YUVEZZI as first dual-agent eye drop for presbyopia
Summit Therapeutics' BLA for ivonescimab in EGFR-mutated NSCLC accepted by FDA
WuXi Biologics collaborates with Sinorda Biomedicine for antibody development
Biogen's litifilimab receives FDA Breakthrough Therapy Designation for CLE
Glaukos receives FDA approval for repeat administration of iDose TR
Guerbet's contrast agent Elucirem approved by European Commission in children from birth
Spine Innovation's LOGIC Titanium Implant System receives US FDA 510(k) market approval