Danish pharmaceutical company Novo Nordisk has announced that the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use (CHMP) has recommended the marketing approval for its NovoEight (turoctocog alfa), ...
Tags: Novo Nordisk, Novoeight
Amerinet, a national healthcare solutions organization, has signed an agreement with All Medical Solutions (AMS), the Healthcare division of Fusion Systems North America, to make the AMS SPHER, a health insurance portability and ...
German-based JenaValve Technology has obtained CE Mark approval for its transapical transcatheter aortic valve implantation (TAVI) system, designed to treat aortic insufficiency (AI). AI, also known as aortic regurgitation, is a condition ...
US-based orthopedics services provider Dallen Medical has filed 510(k) application with the US Food and Drug Administration (FDA) for individually packaged, sterile Compressyn staple implants. The Compressyn staple implant delivers ...
Tags: Compressyn Staple Implant, Health, Medicine
NeoTract has received an approval from the US Food and Drug Administration (FDA) to market its UroLift system, designed to relieve low or blocked urine flow in men age 50 and older with an enlarged prostate (benign prostatic hyperplasia). ...
Tags: Prostate Implant, Neotract
Arch Biopartners (Arch) has received US patent for its brain tumor cell targeting technology, which protects novel synthetic peptides that target and attach human brain tumor initiating cells (BTICs) and invasive glioma cells (IGCs). The ...
It has been reported in R&D that a new type of LED is currently being worked on by a team from The Ohio State University. It comes at a time when commercial uses for UV light are growing, and it is believed the product could be used for ...
NanoString Technologies, a provider of life science tools for translational research and molecular diagnostic products, has obtained the US Food and Drug Administration (FDA) 510(k) clearance for its Prosigna breast cancer prognostic gene ...
The patent-pending LED creates a more precise wavelength of UV light than today's commercially available UV LEDs, and runs at much lower voltages and is more compact than other experimental methods for creating precise wavelength UV light. ...
Tags: Ultraviolet LED
Tenaxis Medical, a developer of high-performance sealants, has received approval to expand its CE Mark indications for ArterX surgical sealant, from its EU notified body, BSI. ArterX Surgical Sealant is specifically designed to be applied ...
Clinics are flooding all over the market however, only few Podtriatric clinics can be found. The importance of knowing any podiatric clinic for any emergencies that can happen anytime. There are certain foot problems that are arising every ...
Tags: foot problem expert
US-based Fujifilm SonoSite received CE mark approval for its X-Porte ultrasound kiosk, a new generation of point-of-care ultrasound. This integrates advanced signal processing for high-resolution imaging, 3D animated clinical guides, and ...
Tags: SonoSite, Ultrasound Kiosk
Biomet Orthopedics has announced the first clinical use of its Signature patient-specific glenoid instrumentation in the US, which is designed to improve placement for total and reverse shoulder arthroplasty. The Signature glenoid system ...
Tags: Biomet Orthopedics, Glenoid System
SpineGuard, a developer of handheld surgical device for spine surgery, has obtained regulatory Ninsho approval to sell its PediGuard platform in Japan PediGuard is reportedly the only handheld device that is capable of alerting surgeons ...
Tags: Pediguard Platform, Medicine
Octapharma USA, part of Swiss human protein products maker Octapharma Group, has announced the availability of Octaplas, a solvent/detergent treated pooled human plasma, in the country. Designed to reduce the risk of pathogen transmission ...
Tags: protein products, Octapharma