BEUDAMED
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    Lumenis brand Atlas, Corium, Elite, Elite Ultra 532nm Laser Systems; Manufactured before November 4, 2003; Manufactured by Lumenis, Inc., 3959 West 1820 South, Salt Lake City, Utah 84104

    FDA Recall
    Terminated ·Lumenis Inc.·Product code GEX·February 1, 2006

    Lumenis brand DuoTome SideLite 550 Micron Delivery System; laser systems for ablating soft tissue. Catalog Number: 0641-800-01; Manufactured by Lumenis, Inc., 2400 Condensa Street, Santa Clara, CA

    FDA Recall
    Terminated ·Lumenis Inc.·Product code GEX·August 29, 2006

    Endo Ocular Directional Laser Probe, Lumenis Inc. Salt Lake City, UT STERILE EO

    FDA Recall
    Terminated ·Lumenis, Inc.·Product code HQF·July 27, 2010

    Lumenis brand LightSheer Pulsed Diode Array Laser System; All serial numbers; Manufactured by RH USA, Inc., 201 Lindbergh Avenue, Livermore, California 94551

    FDA Recall
    Terminated ·Lumenis Inc.·Product code GEX·February 9, 2006

    Vision One Laser System Model GA-0025020, Serial No: 10050, 10051, 10053. Intended for use in the treatment of ocular pathology.

    FDA Recall
    Terminated ·Lumenis, Inc.·Product code GEX·August 19, 2013

    IPL Coupling Gel, I L (AX1009013), 12 pack of 0.25 L (AX1009018), 6 pack of 1 L (AX1009019 or AX1009063); and IPL Coupling Gel or EcoGel 200, 0.25 L (AX1009012) manufactured by Eco-Med Pharmaceutical

    FDA Recall
    Terminated ·Lumenis, Inc.·Product code ITX·October 14, 2021

    Lumenis brand Lumenis One System with Multi-Spot Nd:YAG, LightSheer and Universal IPL; Manufactured by Lumenis, Ltd, 13 Hayetzira Street, Yokneam Industrial Park, Yokneam, Israel 20692

    FDA Recall
    Terminated ·Lumenis Inc.·Product code GEX·April 8, 2005

    Boston Scientific SlimLine 200 Micron Holmium Fiber Delivery Device, Catalog No. 840-840, Sterile, Made In Israel, Manufactured By LUMENIS, P.O.Box 240, Yokneam, ISRAEL.

    FDA Recall
    Terminated ·Lumenis, Inc.·Product code GEX·December 18, 2007

    Array LaserLink, Manufactured by Lumenis, The Array" LaserLink" is a laser system accessory intended for use in the treatment of ocular pathology. " For the Posterior Segment, the Array" LaserLink" is indicated for use in Retinal Photocoagulation and Panretinal Photocoagulation of Vascular and Structural Abnormalities of the Retina and Choroid including: " Proliferative and Severe and Very Severe Non-Proliferative Diabetic Retinopathy " Macular Edema associated with Proliferative or Non-Proliferative Diabetic Retinopathy " Choroidal Neovascularization " Retinal Neovascularization associated with Retinal Occlusive Disease (Branch Retinal Vein Occlusion; Central Retinal Vein Occlusion) " Macular Edema associated with Branch Retinal Vein Occlusion " Retinal Tears and Detachments And Anterior Segments as follows: " Iridotomy in Closed Angle Glaucoma " Trabeculoplasty in Open Angle Glaucoma

    FDA Recall
    Terminated ·Lumenis, Inc.·Product code HQF·August 15, 2014

    LuMend brand percutaneous catheter .35'' R in plastic sealed bag, sterilized with ethylene oxide gas.

    FDA Recall
    Terminated ·Lumend Inc·Product code DQY·May 18, 2004