Vital Access, a provider of surgical and interventional technologies, has launched SAVE-2 post-market clinical follow-up study to investigate the benefits of VWING vascular needle guide for self-cannulation. The SAVE-2 study follows the ...
US-based OrthoSensor has announced its plans to launch its Verasense knee system in European markets after recently receiving CE Mark approval. US-based OrthoSensor has announced its plans to launch its Verasense knee system in European ...
Tags: Verasense Knee System
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
Reverse Medical has received the 510(k) clearance from the US Food and Drug Administration (FDA) for its MVP Micro Vascular Plug system, which is designed for peripheral artery embolization. MVP Micro Vascular Plug system is used to ...
Tags: Reverse Medical, Medicine
Quantel Medical has received the U.S. Food and Drug Administration (FDA) approval for its selective laser trabeculoplasty (SLT) glaucoma laser for clinical use, called Solutis. Solutis is a 532nm SLT laser designed for primary open angle ...
Tags: Quantel Medical, Glaucoma Laser
RTI Surgical, a manufacturer of orthopaedic and other biologic implants, has launched Tritium Sternal Cable Plating (SCP) system for closing median sternotomies following open heart procedures. The device incorporates the advantages of ...
Tags: RTI Surgical, Cable Plating System
The US Food and Drug Administration (FDA) has urged medical device manufacturers to boost their security protection systems against cyber attacks, which could compromise the safety and privacy of patients. According to the agency's safety ...
Tags: Medical Devices, Cyber Attacks
Abyrx, a US-based therapeutic device company, has received the US Food and Drug Administration (FDA) approval for its new Absorbable Hemostatic Bone Putty (AHBP) for clinical use. AHBP is a surgical ready-to-use product which achieves ...
Tags: Abyrx, Bone Putty
Medical device makers should take new steps to protect their products from malware and cyberattacks or face the possibility that U.S. Food and Drug Administration won't approve their devices for use, the FDA said. The FDA issued new ...
Analytical technologies provider AB SCIEX has launched the 3200MD CE-IVDD series for general in vitro diagnostic use in Europe. The new AB SCIEX API 3200MD and 3200MD QTRAP LC/MS/MS systems will help European hospitals and clinical ...
Tags: AB SCIEX, Diagnostic Devices
Reverse Medical has announced the CE Mark approval and initial clinical use of its MVP Micro Vascular Plug system for peripheral artery embolization. MVP Micro Vascular Plug system is used to obstruct or reduce the rate of flow of blood ...
Tags: Reverse Medical, Peripheral
Ventripoint Diagnostics has obtained CE mark certification from European notified body Intertek Semko for its NRV application for the VMS-2DE heart analysis system. The NRV database can be used in conjunction with right heart analysis ...
Tags: Ventripoint, CE Mark, NRV Application
RaySearch Laboratories has launched a new version of its RayStation treatment planning system for clinical use in the European Union, the US, Japan and Australia. The new RayStation 3.5 version includes a wide range of new features and ...
Volition has announced a new collaboration with the Wales Cancer Bank,with the two businesses set to carry out an internal clinical study for the Nucleosomics diagnostic products. At the end of this month,tests will be carried out on ...
Tags: Volition, Wales Cancer Bank, Nucleosomics diagnostic products
Life sciences company VolitionRx has introduced epigenetic immunoassays, designed for identifying and measuring nucleosome structures in cell culture, serum, plasma or other biofluids. Designed for research use, the NuQ immunoassay ...
Tags: VolitionRx, epigenetic immunoassays, clinical technology