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Nerites Corporation and the Midwest Orthopaedic Research Foundation (MORF) announced that they have signed an agreement to co-develop Nerites proprietary technologies for use as surgical adhesives and implant coatings.
ThermoGenesis Corp. announced that the Company entered into a development, license and supply agreement with Biomet Biologics, Inc., a wholly owned subsidiary of Biomet, Inc.
The Centers for Medicare & Medicaid Services (CMS) recently proposed payment changes for home-use oxygen equipment, oxygen contents and capped rental durable medical equipment.
HHS is excluding device and drugmakers from a new protection from the anti-kickback statute designed to promote adoption of electronic health records, arguing that these sectors cannot be trusted to abide by the law.
Galesburg Orthopedic Services did not obtain written consent from patients before implanting its devices, nor did it obtain FDA and institutional review board (IRB) approval before allowing patients to participate in clinical trials, the FDA said in a recent warning letter.
Moeller Medical, LLC announced Tuesday its distribution of an FDA-cleared electrical device that effectively treats depression, anxiety, insomnia, and pain.
Disc Dynamics Inc. announced it has received U.S. Food and Drug Administration (FDA) approval to commence a clinical study of its DASCOR Disc Arthroplasty System.
Predictive medicine company PreMD announced that its second-generation spectrometer, or color reader, for the PREVU* Point of Care (POC) Skin Sterol Test now has the Conformité Européene (CE) Mark.
Shares of Cyberonics dropped 26 percent Tuesday after the company said it is unlikely to make a profit until after an investigation into stock options issued in 2004 is completed.