Posts by rw-admin
Promising Remote Patient Monitoring solution, Polso, Achieves 1st FDA Clearance
ChroniSense Medical Ltd. took a step towards its vision of transforming chronic care management with Polso™, the company’s Remote Patient Monitoring (RPM) solution, achieving 510(k) clearance from the U.S. Food and Drug Administration (FDA). Initial indications include monitoring of blood oxygen saturation (SpO2), pulse rate and respiration rate. “FDA clearance is a significant milestone towards…
Read MoreLazurite is Recognized in the 2022 Medical Device Network Excellence Awards & Rankings for its ArthroFree™ System
Medical device and technology company Lazurite has received recognition from Medical Device Network Excellence Awards & Rankings, one of the largest, most prestigious, and widely recognized programs in the industry. Lazurite ranked as Commended for the Innovation, Product Launches and Research and Development categories. All Commended companies will be entered into the Medical Device Network…
Read MoreActiv Surgical Secures CE Mark Approval for ActivSight™ Intelligent Light
Activ Surgical, a digital surgery pioneer, announced that it is has received CE Mark approval for its ActivSight™ Intelligent Light (“ActivSight”). The CE Mark validates that ActivSight meets the requirements of the European Medical Devices Regulation, allowing Activ Surgical to commercialize the enhanced imaging system across the European Union and other CE Mark required regions.…
Read MoreWISE Receives FDA Clearance for its WISE Cortical Strip Bringing Neuromonitoring to the Next Level
WISE Srl, a medical device company developing next-generation implantable electrodes for neuromonitoring, neuromodulation and brain-machine interfacing (BMI), announced the FDA clearance of its WISE Cortical Strip (WCS®), a single use medical device intended to be used on the brain surface for Intra Operative Neurophysiological Monitoring (IONM). The WISE Cortical Strip is the first product receiving FDA…
Read MoreHemosonics Awared FDA 510(k) Clearance for Quantra® Hemostasis System with QSTAT® Cartridge
HemoSonics, LLC, a leading medical device company delivering individualized diagnostic solutions for Patient Blood Management (PBM), announced that it has received 510(k) market clearance from the U.S. Food and Drug Administration (FDA) for the Quantra Hemostasis System with QStat Cartridge. “The Quantra Hemostasis System with QStat Cartridge is breaking new ground and leading innovation in the…
Read MoreDesert Imaging Deploys densitas® intelliMammo™ A.I. Solutions for Breast Screening Services
Densitas® Inc., a global provider of A.I. solutions for digital mammography and breast screening announced that Desert Imaging has implemented the densitas® IntelliMammo™ platform across their health system. The adoption of intelliMammo™ reinforces Desert Imaging’s established commitment to maintaining robust organization-wide quality improvement initiatives. IntelliMammo™ provides Desert Imaging with on-demand actionable information and streamlined workflows to establish…
Read MoreNeuroLogica Announces FDA 510(k) Clearance of BodyTom® 64
NeuroLogica Corp., a subsidiary of Samsung Electronics Co. Ltd., announced that its head-to-toe trauma imaging solution, the BodyTom® 64 Point-of-Care Mobile Computed Tomography (CT) Scanner, has received 510(k) clearance from the U.S. Food and Drug Administration for commercial use in the United States. “We’re thrilled to build off our expertise and elevate point-of-care imaging with…
Read MoreWhat Are You Thankful For? | Legacy MEDSearch 2022
The holiday season always brings a time of family, friends, good food, and also reflection on the year. This year as we are in the season of giving thanks, we asked our team what everyone was thankful for this holiday season. Here is what they had to say! “I’m thankful for my family; my wife…
Read MoreChoiceSpine™ Announces Line Extension of their Harrier™ Stand-Alone Anterior Lumbar Interbody Fusion System
ChoiceSpine LLC, a privately-held spinal device manufacturer based in Knoxville, TN, announces the launch of an additional lordotic offering for their stand-alone anterior lumbar interbody – Harrier SA. Harrier SA is a 3D printed stand-alone screw-based system incorporating ChoiceSpine’s proprietary BioBond™ porous structure technology. The system has had great success since launching in May of…
Read MoreNew View Surgical, Inc. Closes $12.1M Series B-1 Financing, Readies Limited Market Release of its VisionPort™ System For Minimally Invasive Surgery
New View Surgical, Inc., an emerging medical device company developing proprietary imaging and access technologies for minimally invasive surgery (MIS), announced the closure of a $12.1M Series B-1 equity financing round to fund the commercialization of its VisionPort™ System. The company expects to launch the VisionPort System in the US before the end of 2022.…
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