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ViaCell, Inc. and Pall Corporation announced today the first U.S. Food and Drug Administration clearance of a cord blood collection bag suitable for use in a sterile field.
Higher sales of Kinetic Concepts Inc.'s flagship V.A.C. wound-healing device led to a 31 percent increase in first-quarter earnings, the company said Tuesday.
Endologix has received FDA approval to market new short body-short limb variants of the PowerlinkSystem endoluminal stent graft (ELG) for the minimally invasive treatment of abdominal aortic aneurysms (AAA).
The FDA and the National Institute for Occupational Safety and Health (NIOSH) have issued a public health notice about the "danger of fires at the interface of oxygen regulators and cylinder valves because of incorrect use of CGA 870 seals."
The Confederation of Indian Industries (CII) would urge the Centre for amending the proposed medical devices regulation as it was likely to hit the medical instrument manufacturing and trading sector,
following imposition of huge registration fee.
Cardiac Science Corporation has shipped two new models of its Powerheart automated external defibrillators (AEDs) that meet new American Heart Association (AHA) guidelines for cardiopulmonary resuscitation and emergency cardiovascular care, as well as the recently released European Resuscitation Council (ERC) guidelines for resuscitation.
St. Francis Medical Technologies, Inc. nnounced today the national launch of its patented X STOP Interspinous Process Decompression (IPD) System (" STOP").
They're robots, they're tiny and they're going to do surgery ... in space. While this scenario might sound like a tagline for a 1980s B-movie, it's far from fantasy for researchers at the University of Nebraska at Lincoln and the University of Nebraska Medical Center in Omaha.