Vitls Inc., a company out of Houston, Texas, won FDA clearance for its Vitls Platform, a combination of a vitals monitoring patch, cloud storage, and an app that lets clinicians monitor multiple patients wearing such a patch at once....
Wearable bioelectronic devices that stick to the skin and measure things such as temperature, heart rhythms, and other vitals are typically complex devices that use modern materials to do their job. They tend to be difficult to manufacture,...
The COVID-19 pandemic has led to the implementation and use of telemedicine and telehealth platforms and devices as part of current day-to-day standards of care in many hospital and healthcare systems. In this era of social distancing, doctors...
Getinge has won FDA clearance for its Servo-air mechanical ventilator. The device doesn't need any wall gas or pressurized gas cylinders to operate thanks to a built-in turbine that generates enough continuous air pressure to meet any patient's...
ivWatch, a company based in Newport News, Virginia, won FDA clearance for its SmartTouch sensor that detects peripheral IV infiltration and extravasation events. Though somewhat rare, these can be difficult to notice and a late response can...
Neopenda, a medical device startup based in Chicago that has been featured on Medgadget previously, has recently adapted its wearable vital signs monitor, originally developed for newborns, to be used with pediatric and adult patients in...
Anemia is properly diagnosed using a blood test that measures hemoglobin, but simply looking behind a patient's eyelid can be a pretty good alternative if you know how red the tissue is supposed to be. Now, a team at Purdue University has...
According to the World Health Organization, 47% of childhood deaths worldwide occur in the first four weeks of life. This neonatal mortality rate is particularly prevalent in sub-Saharan Africa, where nearly one million newborns die every...
ABM Respiratory Care, a company with offices in USA, Singapore, and India, announced that it has received FDA 510(k) clearance to market its BiWaze Cough System, a device for removing secretions in patients who are unable to cough or clear...
To help address the COVID-19 emergency that's taking over emergency rooms and intensive care units in the United States, the FDA has cleared the RAPIDPoint 500e blood gas system from Siemens Healthineers.
The device uses the company's...
While current concern is all about the COVID-19 virus that originated in China and spread around the world, this pathogen will eventually disappear. Escherichia coli (E. coli) bacteria, though, is with us for the long run and it can cause just...