BEUDAMED
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    ARK SURGICAL

    FDA registration
    ARK SURGICAL·2 products·🇮🇱 Israel

    LapBox Power

    FDA UDI
    ARK SURGICAL LTD·07290118830023·The LapBox Power Contained Tissue Extraction Sy...

    LapBox Tissue Containment Removal System

    FDA UDI
    ARK SURGICAL LTD·07290118830009·The LapBox Tissue Containment Removal System is...

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code MJP·February 2, 2026

    EVO/EVO+VISIAN IMPLANTABLE COLLAMER LENS

    FDA Adverse Event
    Injury ·STAAR SURGICAL COMPANY·Product code QCB·November 7, 2025

    TECNIS 1 MULTIFOCAL

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code MFK·February 25, 2020

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code MFK·April 18, 2025

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO PUERTO RICO MFG. INC.·Product code MFK·April 18, 2025

    TECNIS 1-PIECE IOL WITH TECNIS SIMPLICITYTM DELIVERY SYSTEM

    FDA Adverse Event
    Malfunction ·AMO PUERTO RICO MFG. INC.·Product code HQL·October 30, 2025

    TECNIS SYMFONY TORIC

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON SURGICAL VISION, INC.·Product code POE·July 3, 2019

    LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM VG

    FDA Adverse Event
    Injury ·ALLERGAN·Product code LTI·August 27, 2013

    TECNIS IOL

    FDA Adverse Event
    Injury ·AMO MANUFACTURING NETHERLANDS·Product code MFK·February 2, 2026

    CS Life Sciences Europe Ltd

    Authorized representative
    🇮🇪 Ireland·35 Manufacturers·444 Devices

    Emergo Europe B.V.

    Authorized representative
    🇳🇱 Netherlands·900 Manufacturers·22100 Devices

    C ARM SURGICAL TABLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    HEMI-ARC SURGICAL NAVIGATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    ARC SURGICAL BIOTRAK SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARC SURGICAL BONE REDUCTION SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ARC SURGICAL BIOTRAK PIN SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SURGICAL PHACOEMULSIFICATION P ACK

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB, INC.·Product code HQC·April 3, 2007