Lumenis Limited has recalled certain models of its VersaCut morcellator to make a labeling correction, the US Food and Drug Administration (FDA) announced February 25. Morcellators are used to cut and ...
Israel's Lumenis faces a Class I FDA recall over certain models of the company's VersaCut Morcellator devices, which are used to break up and remove dissected tissue during surgery when there is ...
Israel's Lumenis is bucking the hesitance of many medical device companies to pursue the public markets and is moving ahead with its U.S. IPO plans. The maker of minimally invasive medical lasers ...
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