BEUDAMED
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    ARP POV SPORT

    FDA UDI
    ARP MANUFACTURING LLC·M7570010880·Electrical Muscle Stimulator intended to stimul...

    ARP POV SPORT

    FDA UDI
    ARP MANUFACTURING LLC·M7570040000·Electrical Muscle Stimulator intended to stimul...

    ARP POV SPORT

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    Identity Imprint Porous CR

    FDA UDI
    Conformis, Inc.·M572POV0124411011·POROUS OVAL PATELLA, 44MM X 11MM, iPoly

    Identity Imprint Porous CR

    FDA UDI
    Conformis, Inc.·M572POV0124110011·POROUS OVAL PATELLA, 41MM X 10MM, iPoly

    ITOTAL UHMWPE 44MM X 11MM CEMENTED OVAL PATELLA IMPLANT

    FDA UDI
    Conformis, Inc.·M572POV0114411011·

    Identity Imprint Porous CR

    FDA UDI
    Conformis, Inc.·M572POV0123208011·POROUS OVAL PATELLA, 32MM X 8MM, iPoly

    TOTAL IPOLY XE 29MM X 7MM CEMENTED OVAL PATELLA IMPLANT

    FDA UDI
    Conformis, Inc.·M572POV0212907011·

    Identity Imprint Porous CR

    FDA UDI
    Conformis, Inc.·M572POV0123509011·POROUS OVAL PATELLA, 35MM X 9MM, iPoly

    ITOTAL IPOLY XE 32MM X 8MM CEMENTED OVAL PATELLA IMPLANT

    FDA UDI
    Conformis, Inc.·M572POV0213208011·

    Identity Imprint Porous CR

    FDA UDI
    Conformis, Inc.·M572POV0123809011·POROUS OVAL PATELLA, 38MM X 9MM, iPoly

    ETNIA EYEWEAR CULTURE

    FDA UDI
    Etnia Barcelona, Llc.·08435736081313·Frame Spectacle

    ETNIA EYEWEAR CULTURE

    FDA UDI
    Etnia Barcelona, Llc.·08435736081351·Frame Spectacle

    ETNIA EYEWEAR CULTURE

    FDA UDI
    Etnia Barcelona, Llc.·08435736081276·Frame Spectacle

    ETNIA EYEWEAR CULTURE

    FDA UDI
    Etnia Barcelona, Llc.·08435736081399·Frame Spectacle

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·September 22, 2014

    DISPOSABLE ELECTROSURGICAL SNARE

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code FDI·October 15, 2025

    CARDIOSAVE

    FDA Adverse Event
    Death ·DATASCOPE MAHWAH·Product code DSP·March 21, 2018

    HALOTECH G2 KIT

    FDA Adverse Event
    Malfunction ·HALOTECH, SRL. / HALOTECH DNA SL·Product code POV·September 17, 2020

    WAVELIGHT EX500 EXCIMER LASER

    FDA Adverse Event
    Injury ·WAVELIGHT GMBH·Product code LZS·August 5, 2020