Johnson & Johnson announced U.S. 510(k) regulatory clearance for MONARCH QUEST 3, the latest software update for the MONARCH Platform. The update reflects the company’s continued commitment to… read more.
Premarket evidence and regulatory characteristics offered little predictive value, researchers report in JAMA Health Forum More than one-third of high-risk therapeutic medical devices authorised for use in the… read more.
Royal Philips announced FDA 510(k) clearance of its next-generation reusable Philips SpO₂ clip sensor, reinforcing the company’s ongoing commitment to providing clinicians with trusted oxygen saturation measurements that… read more.
4 August 2026 – GE HealthCare announced the introduction of the Logiq e family, featuring Logiq e Xi and Logiq e Si, two compact laptop ultrasound systems designed… read more.
Abbott announced a first-of-its-kind partnership with Google Health to redefine how people understand and manage their health. By combining glucose insights from Abbott’s Lingo biowearable with Google’s expertise… read more.
GE HealthCare announced the launch of Invenia Abus (Automated Breast Ultrasound) Prime and Abus StreamVue, a redesigned enterprise viewer that recently received FDA 510(k) clearance and CE Marking,… read more.
Medtronic announced an expanded CE Mark indication for the Affera Mapping and Ablation System with Sphere-9 Catheter to treat ventricular arrhythmias, including ventricular tachycardia (VT) and premature ventricular… read more.
Johnson & Johnson announced that the FDA has granted De Novo authorization for the OTTAVA Robotic Surgical System, the world’s first table-integrated soft tissue robotic system. The system… read more.
Researchers have developed a breath detector with a chemical sensor that sniffs out when your body is burning fat through a single exhale. Reporting on July 22 in the Cell Press journal Device, the… read more.
Johnson & Johnson announced the first robotically-assisted bronchoscopy case in the Middle East using the MONARCH Platform. The procedure, which took place at the Cleveland Clinic Abu Dhabi,… read more.
Chiesi announces MHRA approval in the UK of Clenil Modulite (beclometasone; 100 mcg and 200 mcg) formulated with a next-generation, non-PFAS, low GWP propellant. These are the first… read more.
Johnson & Johnson announced that the FDA approved the Dual Energy THERMOCOOL SMARTTOUCH SF Platform (DE STSF), an integrated catheter ablation solution that enables electrophysiologists to deliver both… read more.
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