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    • Malvina Eydelman

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    Many LASIK patients have new eye problems after surgery: JAMA Opthalmology Study

    Many LASIK patients have new eye problems after surgery: JAMA Opthalmology Study

    supriya kashyap kashyap25 Nov 2016 12:19 PM IST
    Washington : A significant percentage of people who undergo LASIK eye surgery to correct their vision may experience side effects from the surgery,...
    Now auto adjustable lens after cataract surgery

    Now auto adjustable lens after cataract surgery

    Anjali Nimesh Nimesh23 Nov 2017 8:00 PM IST
    The U.S. Food and Drug Administration approved the RxSight Inc. Light Adjustable Lens and Light Delivery Device, the first medical device system that...
    FDA clears first Photochromatic contact lens

    FDA clears first Photochromatic contact lens

    Ruby khatun khatun11 April 2018 7:35 PM IST
    The U.S. Food and Drug Administration has cleared the first F Photochromatic contact lens,a lens with an additive that automatically darkens the lens...
    First AI based medical device to detect diabetic retinopathy approved

    First AI based medical device to detect diabetic retinopathy approved

    Dr. Kamal Kant Kohli Kohli11 April 2018 8:00 PM IST
    The IDx-DR device, from IDx LLC, is the first device which has been authorized for marketing by U.S. Food and Drug Administration that provides a...
    FDA approves first Prosthetic Iris

    FDA approves first Prosthetic Iris

    Vinay Singh singh31 May 2018 7:20 PM IST
    The US Food and Drug Administration approved the first prosthetic iris to treat patients with aniridia or other damages to the eye. The surgically...
    User friendly, Self-fitting hearing aid approved by FDA

    User friendly, Self-fitting hearing aid approved by FDA

    Hina Zahid6 Oct 2018 8:10 PM IST
    A new user-friendly hearing aid intended to amplify sounds for individuals 18 years or older with perceived mild to moderate hearing impairment has...
    FDA allows marketing of new device to help treat carbon monoxide poisoning

    FDA allows marketing of new device to help treat carbon monoxide poisoning

    Hina Zahid18 March 2019 7:10 PM IST
    The U.S. Food and Drug Administration today allowed marketing of a new device, ClearMate, intended to be used in an emergency room setting to help...

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