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  • LASEROPTEK 's PicoLO™ Picosecond Nd:YAG Laser Receives FDA 510(k) Clearance

    LASEROPTEK’s PicoLO recently received U.S. FDA 510(k) clearance. the PicoLO clearance will help that LASEROPTEK significantly increase its sales in the U.S. market. C.J. Lee, CEO and President of LASEROPTEK, said that “PicoLO's technology-rich DNA in combination with LASEROPTEK's world class technical and clinical support will garner the attention of dealers, physicians and patients.” https://www.prnewswire.com/news-releases/laseroptek-co-ltds-picolo-picosecond-ndyag-laser-receives-fda-510k-clearance-for-use-in-dermatology-and-general-and-plastic-surgery-300793732.html?fbclid=IwAR0D9W5vixUEzibe9vDlAuO5SCu16XMeiSbN055FjdGXfy-wnlXc9lH7Hp8

    2019.2.12