BEUDAMED
    3 results · 35ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters FDA Recall ×

    Aerolase Corporation. The products involved are the FriendlyLight YAG lasers, a Model Family first identified and reported. The products are marketed under names including FriendlyLight Er:YAG, LightPod Era, FriendlyLight Nd:YAG, LightPod Neo, LightPod Neo XL, LightPod Neo XT, LightPod Forte, LightPod Allure, and LightPod Nova.

    FDA Recall
    Terminated ·Aerolase·Product code GEX·June 7, 2011

    LightPod Neo Lasers

    FDA Recall
    Terminated ·Aerolase Corporation·Product code GEX·August 1, 2019

    LightPod ERA lasers

    FDA Recall
    Terminated ·Aerolase Corporation·Product code GEX·August 1, 2019