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The device is said to be clinically proved as a high-level disinfect for commonly used endoscopes such as duodenoscopes. The AER uses an advanced pass-through design that facilitates
The US Food and Drug Administration (US FDA) approved the full system in October 2017. The system, which features the SenTiva generator and next-generation Programming System, is intended for for the treatment
The investors syndicate who provided the funding include Andera Partners, Panakes Partners and Fountain Healthcare returning Seed investor Sambatech, and two industry veterans Gus Castello, former Senior Vice
The embolization spheres, which are manufactured by Teleflex subsidiary Vascular Solutions, are designed as a resorbable embolic alternative treatment option to permanent embolics. Hypervascular tumors, which are present as
The series C financing has been designed to fund the company via pre-market approval (PMA) of the Tack system. New Enterprise Associates (NEA), H.I.G. BioVentures and Quaker Partners
Boston Scientific is paying $150m up front and another $125m in milestone payments over four years to acquire nVision. nVision has developed Mako 7 device, which uses patented microcatheter
The specially coated urinary catheter will be studied in six hospitals across the UK, in a bid to determine whether predicting laboratory results transform into significantly reduced infection
The new CyPass ultra system has been developed to streamline the process of loading the MIGS device. CyPass system enables to decrease the multiple steps required to implant
The Spineology clinical outcomes trial (SCOUT), which was carried out under an FDA-approved IDE protocol, is a multicenter and non-randomized performance goal investigation study designed to assess safety
The approval was based on results of the Inspire study, which is a controlled clinical organ preservation trial carried out at 21 international academic institutions. The trial compared the