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An Evolution in Automated CO2 Laser Surgery
Date:1/5/2009

Lumenis announces 510(k) approval for the new AcuPulse CO2 Laser with SurgiTouch Automation System

SANTA CLARA, Calif., Jan. 5 /PRNewswire/ -- Lumenis Inc., a global developer, manufacturer and seller of laser, light-based and radiofrequency devices for surgical, aesthetic, and ophthalmic applications, announced today the FDA approval and market introduction of its new AcuPulse CO2 Laser for ENT, Gynecology, Neurosurgery, General Surgery and Aesthetic medicine.

AcuPulse represents an evolution in automated CO2 laser surgery. Benefiting from years of experience with the Sharplan Compact product line, the AcuPulse was designed to create a new standard in treatment convenience for the physician and the nursing staff alike. Considering human factors and efficacy as major concept goals, automation and robotics features are controlled from a large area video screen that assures simple communication with the user.

"We are pleased to provide the groundbreaking AcuPulse with the SurgiTouch automation system," said Mr. Dov Ofer, Lumenis' Chief Executive Officer. "Physicians can achieve reproducible outcomes at the push of a button by simply selecting the laser application on an intuitive user interface. A mix of animated and real videos can be displayed showing various laser procedures, allowing for quick familiarization across specialties."

With the AcuPulse CO2 laser and SurgiTouch automation system, surgeons can now focus on the surgery - not the laser set-up. Attention has also been paid to the needs of the operating room staff. Video animations display the assembly instructions for various laser accessories, making it simple for new staff to become quickly familiar with the system. "In a busy environment like ours where many nurses rotate between operating rooms, this is an invaluable feature that assure quick readiness of the AcuPulse and improves operating room turn over. In addition, I like i
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SOURCE Lumenis Inc.
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