BEUDAMED
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    da Vinci SP Surgical System (SP1098)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CoRoent

    FDA UDI
    Nuvasive, Inc.·00887517579058·CoRoent Ant TLIF Ti, 15x11x32mm 4°

    FAA Airline - 24 Poly White

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588013244·FAA Airline - 24 Poly White

    Symmetry Surgical

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482062432·Instrument Tray 13 X 24 X 3 1/2"

    ATTUNE

    FDA UDI
    DEPUY (IRELAND)·10603295439035·ATTUNE KNEE SYSTEM REVISION PRESS-FIT STEM TRIA...

    ATTUNE

    FDA UDI
    DEPUY (IRELAND)·10603295439011·ATTUNE KNEE SYSTEM REVISION PRESS-FIT STEM TRIA...

    ATTUNE

    FDA UDI
    DEPUY (IRELAND)·10603295439028·ATTUNE KNEE SYSTEM REVISION PRESS-FIT STEM TRIA...

    Straumann Variobase for CEREC

    FDA 510(k)
    FDA Class 2 ·Dental

    MEDI BUTLER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SCISSORS, BLUNT, 5 FR., 34 CM

    FDA Adverse Event
    Malfunction ·KARL STORZ SE & CO. KG·Product code GCJ·July 31, 2025

    BD VACUTAINER® BLOOD COLLECTION TUBES BUFFERED SODIUM CITRATE 0.3ML - 0.109M

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 14, 2018

    AML DURALOC POLY LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code KWB·December 3, 2008

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·August 12, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 29, 2013

    SCISSORS, POINTED, 5 FR., 34 CM

    FDA Adverse Event
    Malfunction ·KARL STORZ SE & CO. KG·Product code GCJ·July 31, 2025