Encora Therapeutics gains FDA clearance for essential tremor device
The US Food and Drug Administration (FDA) has cleared Encora Therapeutics’ neurostimulation wearable for essential tremor (ET) management. The Massachusetts-based company’s …
The US Food and Drug Administration (FDA) has cleared Encora Therapeutics’ neurostimulation wearable for essential tremor (ET) management. The Massachusetts-based company’s …
Abbott has initiated a trial of its Volt pulsed-field ablation (PFA) system at 15 UK National Health Service (NHS) hospitals …
Neurent Medical has closed an oversubscribed Series C financing round, raising €62.5m ($74m) to expand commercial activities for the NEUROMARK …
Natus Sensory has purchased TheraB Medical, a US-based company specialising in neonatal wearable phototherapy devices. The acquisition aims to extend access …
Femtech company Mira is collaborating with ŌURA, allowing users of the Finnish company’s Oura smart ring to access lab-grade hormone …
Edwards Lifesciences has reported revenue over $6bn in full year 2025, predominantly driven by strong demand for its transcatheter aortic …
Asahi Kasei’s ZOLL has received approval for its Zenix monitor/defibrillator under the European Union Medical Device Regulation 2017/745 (EU MDR). The …
Merck KGaA (Merck) and Calla Lily Clinical Care have announced a strategic partnership to advance Callavid, an intravaginal drug delivery …
Zimmer Biomet has achieved revenue of $8.23bn in full year 2025 off the back of continued strong demand across its …
The UK government has set out to improve access to healthcare technology within the National Health Service (NHS) through the …
Becton Dickinson and Company (BD) has trimmed its fiscal year 2026 (FY26) profit outlook to account for the spin-off of …
Traditional randomized controlled trials (RCTs) have long been the gold standard for testing new therapies, but they are increasingly strained …
GE HealthCare has announced the US launch of ReadyFix, a remote fleet management solution designed to help healthcare systems optimise …
TransMedics Group has received full and unconditional investigational device exemption (IDE) approval from the US Food and Drug Administration (FDA) …
The US Food and Drug Administration (FDA) has cleared a lung cancer detection tool on Median Technologies’ eyonis, a suite …