This section presents the latest developments, inventions, and revolutionary technologies that change the face of healthcare.
ElectroWire Medical has received U.S. Food and Drug Administration (FDA) clearance for its LightningWire™ Transseptal Puncture System, marking an important regulatory milestone for the company's cardiovascular device portfolio....
Aidoc has been awarded U.S. Food and Drug Administration (FDA) Breakthrough Device Designation for First Read, an artificial intelligence solution created to assist radiologists by analysing chest radiographs and producing an initial draft of radiology reports. T...
Serenity Medical has secured Breakthrough Device Designation from the U.S. Food and Drug Administration (FDA) for its Serenity Shepherd Stent™ System, reinforcing its progress in the development of neurovascular devices for venous sinus disorders....
Grey Matters Health Inc. has installed its first brain-dedicated Positron Emission Tomography (PET) scanner at its flagship NovaScan Neuroimaging Clinics™ facility in Davie, Florida, supporting the company's expansion into specialised neuroimaging services in the US....
United Therapeutics Corporation has received premarket approval (PMA) from the U.S. Food and Drug Administration (FDA) for its LungFX device, enabling centralised ex vivo lung perfusion (EVLP) to assess donor lungs outside the body before transplantation....
Brooks Instrument has introduced the AMF Series™ Advanced Mass Flow Controller (MFC), an ultra-compact gas flow control solution designed to deliver high performance in space-constrained industrial and research environments....
Cardiawave has announced the first routine clinical treatments using its Valvosoft® system following CE Mark approval, marking the start of the technology’s commercial deployment across Europe....
TETmedical, Inc. has received Breakthrough Device Designation from the U.S. Food and Drug Administration (FDA) for its NSE-FAST® (Neuron Specific Enolase – Functional Activity Stroke Test),...
Florida State University (FSU) and Sky Therapeutics have secured U.S. Food and Drug Administration (FDA) Breakthrough Device Designation for Cenextra, a digital therapy designed to improve executive functioning in children with attention-deficit/hyperactivity disorder (ADHD)....
ElectroWire Medical has received U.S. Food and Drug Administration (FDA) clearance for its LightningWire™ Transseptal Puncture System, marking an important regulatory milestone for the company's cardiovascular device portfolio....
