We use cookies to provide you with a better experience. By continuing to browse the site you are agreeing to our use of cookies in accordance with our Cookie Policy.
The deal nets Canady a robotic needle holder and a 5mm motorized articulated surgery device that enables access to intra-abdominal areas, among other items. Read More
Devicemakers that participate in the Medical Device Single Audit Program (MDSAP) should not have to undergo notified body certification, the committee says. Read More
Acting FDA Commissioner Ned Sharpless said that ACell placed profit above patient safety when it failed to notify the FDA about the product’s recall. Read More
The European Medicines Agency issued a draft guideline on quality requirements for combination devices, opening the guidance up to a three-month public consultation. Read More
After months of criticism of the European Commission for the slow release of guidance on the EU’s new medical device regulations, the Commission released a flurry of documents on the Eudamed data exchange. Read More