Tuesday, January 06, 2015
Dune Medical Devices announced FDA approval of an updated version of its flagship product, MarginProbe, a medical device that enables real-time detection of cancer at the surface of excised tissue specimens during breast-conserving cancer surgery.
Surgeon feedback, innovative design ideas, and superior miniaturization engineering were the driving forces behind the development of MarginProbe 1.2. This new version, which utilizes the same trusted, FDA-approved, diagnostic technology as version 1.1, is focused on proving superior functionality, portability, and overall ease of use.
"Our goal in offering this update is to provide surgeons with the most effective, easy-to-use product when they walk into a lumpectomy case," said Dan Hashimshony, CEO of Dune Medical Devices. "Once the MarginProbe demonstrated national success across all territories, we began enhancing the usability for surgeons while offering simpler handling. Despite the fact that we offer the only product dedicated to the pressing need for intraoperative margin assessment in breast cancer surgery, we always knew it's critical we constantly listen to our loyal and growing customer base and do our best to offer them further innovation."
Feature enhancements for MarginProbe 1.2 include:
Additional information about MarginProbe 1.2 can be found at http://www.marginprobe.com/marginprobe-1-2/ . MarginProbe 1.1 is, and will remain, fully supported by Dune Medical Devices.
About Dune Medical Devices
Dune Medical Devices was founded in 2002 by Dr. Dan Hashimshony to realize the extraordinary medical potential of its proprietary tissue characterization technology. Offering surgeons and radiologists the real time ability to identify cancerous tissues and react immediately, this technology holds the promise for a broad range of surgical and diagnostic applications.
Dune Medical Devices is a privately held company with offices in the U.S. and Israel.
Source : http://www.prnewswire.com