Digital Surgery touts artificial intelligence for the operating room

Officials at Digital Surgery (London) boast that they have successfully demonstrated a real-time, dynamic artificial intelligence (AI) system designed for the operating room. The patented AI platform includes surgical procedure roadmaps that are meant to aid the surgical team in an OR. The goal is to reduce risk and make surgery safer. “This is a huge milestone for

ResMed, Google’s Verily ink sleep-apnea-focused joint venture deal

ResMed (NYSE:RMD) and Google (NSDQ:GOOG) life sciences company Verily said today they inked a new joint venture deal aiming to develop software solutions to improve diagnosis, treatment and care for sleep apnea and other breathing related sleep disorders. The new US-based joint venture will use sleep apnea knowledge from San Diego-based ResMed and Verily’s data analytics technologies in its […]

Medtech stories we missed this week: July 6, 2018

From Zetta getting FDA clearance to Prescient Medical receiving CE Mark approval, here are five medtech stories we missed this week but thought were still worth mentioning. 1. Zetta wins FDA clearance for Zoom MRI software Zetta announced in a June 25 press release that its MRI software has received FDA 510(k) clearance. The software, known as

This algorithm analyzes medical images 1,000 times faster than usual

Massachusetts Institute of Technology researchers have developed an algorithm that makes it easier and 1,000 times quicker to analyze medical images and 3D scans. Medical image registration is a technique that uses two medical images, such as MRI images, to compare and analyze the anatomical differences in detail. In this technique, doctors overlay images from

Medical devices: When should you make them smarter?

The drive toward value in healthcare has increased demand for smarter medical devices able to provide information for real-time feedback, as well as after-the-fact analysis. So when does it make sense to actually make a medical device smarter? And how do you go about it? Tom KraMer, CEO of Kablooe Design outside Minneapolis, has a

Bluebee receives ISO 13485 certification

Bluebee recently announced that it has received ISO 13485 medical device quality standard certification for its design and development of software solutions and data processing algorithms intended for use in diagnostics and clinical reporting. The certification body BSI certified that Bluebee’s design, development, installation, testing and servicing of custom-made software solutions and data processing algorithms

Bay Labs wins FDA clearance for AI-based echocardiogram analysis

Bay Labs has received 510(k) clearance from U.S. FDA for use of its EchoMD AutoEF software product to provide fully automated clip selection and calculation of left ventricular ejection fraction (EF), the San Francisco–based company said today. The EF is the percentage of blood leaving a heart each time it contracts. Bay Labs in its news release

DreaMed Diabetes wins FDA authorization to market insulin therapy management platform

DreaMed Diabetes said today that U.S. FDA has granted a de novo request for DreaMed Advisor Pro, its AI-based diabetes treatment decision support software. The news comes about four months after the Petah Tikva, Israel–based company won CE Mark clearance for the decision-support platform, which is meant to help healthcare professionals manage insulin therapy for people with Type

Medtech stories we missed this week: June 15, 2018

From Cytosorbents opening a new U.S. manufacturing facility to DyAnsys received FDA clearance for a wearable to treat opioid withdrawals, here are seven medtech stories we missed this week but thought were still worth mentioning. 1. Cytosorbents opens new U.S. manufacturing facility CytoSorbents announced in a June 12 press release that it has opened a new

Medtech stories we missed this week: June 8, 2018

From Royal Philips receiving FDA clearance to NeuroPace launching its epilepsy treatment device, here are seven medtech stories we missed this week but thought were still worth mentioning. 1. FDA clears Philips’s Ingenia Elition 3.0T MR scanner Royal Philips announced in a June 5 press release that it has received FDA 510(k) clearance for its Ingenia

Report: IBM Watson Health slashes workforce

International Business Machine (NYSE:IBM) reportedly laid off 50% to 70% of the workforce at its Watson Health operation, primarily at recent acquisitions for which the tech giant paid at least $3.6 billion. The layoffs, according to a May 25 report in The Register, involve Cleveland-based Explorys and Dallas-based Phytel, which IBM acquired in April 2015 for undisclosed amounts. Cleveland […]

Synopsys hosts technical webinar series

Synopsys recently announced that it has launched its 15-minute Technical Webinars to showcase some of the important new features and performance improvements in its Simpleware software version N-2018.03. Simpleware is a 3D imaging software for medical imaging applications. It offers improvements to 3D image visualization, processing and segmentation. The update featured improvements to data analysis

Grayhill launches Touch Encoder Development Kit

Grayhill recently launched its Touch Encoder Development Kit that gives product development engineers simplified designs for medical applications. The new development kit features tap, swipe and turn functions that gives designers the opportunity to replace traditional user-input devices. Using a tablet development app, product development engineers can personalize multi-touch gestures, create images and customize the

Smartphone-based device could detect retinopathy at home

University of California at Berkeley researchers have developed a smartphone-based device that examines the retina and acts as a user-friendly version of the optometrist’s ophthalmoscope. Daniel Fletcher and his students developed the handheld ophthalmoscope by pairing the imaging capabilities of a smartphone with software that is designed to examine the retina. “The advanced technology built

9 exhibitors at DeviceTalks Minnesota you should know

DeviceTalks Minnesota is an annual event that allows some of the best minds in medtech to exchange ideas, insights and technologies. Medical Design & Outsourcing’s parent company WTWH Media holds DeviceTalks annually in Boston, Orange County, Calif., and the Twin Cities in Minnesota. It is hosted by MassDevice and attendees can plan to enjoy networking with people

Pages: 1 2 3 4 5 6 7 8 9 10