BEUDAMED
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    ProSomnus EVO [PH] Sleep and Snore Device, ProSomnus EVO [PH] Sleep and Snore Device with Patient Monitoring

    FDA 510(k)
    FDA Class 2 ·Dental

    Oticon

    FDA UDI
    Oticon A/S·05714464008384·OTICON MORE 3 MINIRITE R C044

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102090·PINNACLE ALTER BEARING INSTRUMENT TRIAL 52OD x ...

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102076·PINNACLE ALTER BEARING INSTRUMENT TRIAL 48OD x ...

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102120·PINNACLE ALTER BEARING INSTRUMENT TRIAL 58OD x ...

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102168·PINNACLE ALTER BEARING INSTRUMENT TRIAL 66OD x ...

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102144·PINNACLE ALTER BEARING INSTRUMENT TRIAL 62OD x ...

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102069·PINNACLE ALTER BEARING INSTRUMENT TRIAL 46OD x ...

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102052·PINNACLE ALTER BEARING INSTRUMENT TRIAL 44OD x ...

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102151·PINNACLE ALTER BEARING INSTRUMENT TRIAL 64OD x ...

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102113·PINNACLE ALTER BEARING INSTRUMENT TRIAL 56OD x ...

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102137·PINNACLE ALTER BEARING INSTRUMENT TRIAL 60OD x ...

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102083·PINNACLE ALTER BEARING INSTRUMENT TRIAL 50OD x ...

    PINNACLE

    FDA UDI
    DEPUY ORTHOPAEDICS, INC.·10603295102106·PINNACLE ALTER BEARING INSTRUMENT TRIAL 54OD x ...

    SURGIFORM AUGMENTATION MATERIAL (S.F.A.M.)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    STAXX XD SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    FLOWART NEEDLE-FREE SPLIT SEPTUM VALVE

    FDA Adverse Event
    Malfunction ·ASSET MEDIKAL TASARIM SAN. TIC. A.S.·Product code FPA·July 24, 2025

    NXSTAGE SYSTEM ONE

    FDA Adverse Event
    Injury ·NXSTAGE MEDICAL, INC.·Product code KDI·November 4, 2008

    UNICEL® DXC 800 PRO SYNCHRON® CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code JJE·August 24, 2011

    CONSTELLATION VISION SYSTEM

    FDA Adverse Event
    Malfunction ·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·July 9, 2013