French brand ZOOOK has launched a state-of-the-art contactless medical grade thermometer developed in accordance with the requirements of COVID-19 patients in India.
Bio-Techne has launched the CE-IVD marked RNA scope In Situ Hybridization Detection Kit for automation on the BOND-III platform in Europe
SMART Medical Systems Ltd announced that the US FDA issued 510(k) clearance for its G-EYE colonoscope.
The US FDA has approved portable X-ray system AiRTouch for human medical use.
4DMedical has received clearance from the US FDA to market its XV Technology, a patented four-dimensional lung imaging process that rapidly and automatically analyses any functional lung impairment from a single X-ray.
CareDx, Inc has received the CE mark for AlloSeq Tx 17. AlloSeq Tx 17 is for matching transplant donor organs to recipients, utilising next generation hybrid capture (HC) technology for HLA testing.
Olympic Ophthalmics announced that the US FDA has granted a De Novo request for iTEAR100, a prescription neurostimulation technology to temporarily increase acute tear production in adults.
The US FDA has approved the next-generation HeartLight X3 Endoscopic Ablation System for the treatment of drug-refractory recurrent symptomatic paroxysmal atrial fibrillation (PAF), CardioFocus announced.
Royal Philips announced the launch of an ultrasound solution for paediatric assessment.
OptiScan Biomedical Corporation announced that the OptiScanner7000 has received CE Mark certification for use in the European Union.
Nipple-sparing mastectomy (NSM) in the United States was first described by Drs. Joseph Crowe and Randall Yetman of the Cleveland Clinic (CCF) in 2004
Soin Neuroscience has developed a new spinal cord stimulation device to treat chronic pain. The company has recently started early-stage human proof of concept studies.
The European and American medical associations have come to a consensus agreement on the definition and diagnosis of neurogenic supine hypertension, recently.
