BEUDAMED
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    ART-M1, MODEL M1-1-ART-A1

    FDA 510(k)
    FDA Class 2 ·Dental

    Sledgehammer

    FDA UDI
    Keystone Industries·H66810005101·SC 1 lb Pwd Original

    CUSTOM PROCEDURE KIT

    FDA UDI
    MEDIVATORS INC.·40677964004665·The ENDO CARRY-ON Procedure Kit contains all of...

    eWave 6-Lead EKG

    FDA UDI
    Wearlinq, Inc.·K00010·Continuous wearable electrocardiogram (ECG) mon...

    MINIMED QUICK-SET

    FDA Adverse Event
    Injury ·UNOMEDICAL A/S·Product code FPA·August 28, 2024

    TI DPL-Recon.Plate 3.5mm,str.,9 H., 128.5mm,locking plate,with combi-holes,

    FDA UDI
    mahe medical gmbh·EMAH10005100090·TI DPL-Recon.Plate 3.5mm,str.,9 H., 128.5m...

    TI DPL-Recon.Plate 3.5mm,str.,8 H., 114.0mm,locking plate,with combi-holes,

    FDA UDI
    mahe medical gmbh·EMAH10005100080·TI DPL-Recon.Plate 3.5mm,str.,8 H., 114.0m...

    TI DPL-Recon.Plate 3.5mm,str.,6 H., 85.0mm,locking plate,with combi-holes,

    FDA UDI
    mahe medical gmbh·EMAH10005100060·TI DPL-Recon.Plate 3.5mm,str.,6 H., 85.0mm...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659257467·TI DPL-Recon.Plate 3.5mm,str.,8 H., _x000D_...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659257481·TI DPL-Recon.Plate 3.5mm,str.,9 H., _x000D_...

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659257429·TI DPL-Recon.Plate 3.5mm,str.,6 H., _x000D_...

    Midmark IQvitals Device Kit w/touchscreen - Blood Pressure, Temperature and SpO2

    FDA UDI
    MIDMARK CORPORATION·00841709100819·Midmark IQvitals is an affordable, Windows base...

    Non-Telescopic PenEvac

    FDA UDI
    I.C. MEDICAL, INC.·00817688020509·

    mahe medical GmbH

    FDA UDI
    mahe medical gmbh·04050659257443·TI DPL-Recon.Plate 3.5mm,str.,7 H., _x000D_...

    TI DPL-Recon.Plate 3.5mm,str.,7 H., 99.5mm,locking plate,with combi-holes,

    FDA UDI
    mahe medical gmbh·EMAH10005100070·TI DPL-Recon.Plate 3.5mm,str.,7 H., 99.5mm...

    PediFlex

    FDA UDI
    ORTHOPEDIATRICS CORP.·00841132133415·PEDIFLEX TITANIUM SET II (IMPLANT, INSTRUMENT, ...

    MODIFICATION TO MODEL 5866-37M LEAD ADAPTOR KIT

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VOYAGER 6.0 SOFTWARE OPTION

    FDA 510(k)
    FDA Class 2 ·Neurology

    0001222315-2025-000510

    FDA Adverse Event
    Injury ·STRAUMANN MANUFACTURING, INC.·Product code DZE·February 24, 2025

    POSSIS SUTURELESS MYOCARDIAL LEAD

    FDA Adverse Event
    Injury ·POSSIS MEDICAL, INC.·Product code LWS·September 20, 1996