BEUDAMED
    2 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Terminated ×

    Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002

    FDA Recall
    Terminated ·Clarus Medical, Llc·Product code GEX·July 27, 2021

    Lase DiscectomLase Discectomy Device Kit, Models 1100-002 and 1100-002 SHORTy Device Kit, Models 1100-002

    FDA Enforcement
    Class II ·Terminated·Clarus Medical, Llc·September 8, 2021