BEUDAMED
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    EQUINOXE REVERSE SHOULDER COMPRESSION SCREW / 38MM AND 42MM GLENOSPHERE / SUPERIOR AUGMENT GLENOID PLATE, 10 DEGREES...

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·July 8, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·March 6, 2019

    EQUINOXE

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·March 26, 2021

    STARLED5 NX

    FDA UDI
    ACEM SPA·08050705890521·STARLED5 NX 2-ARM CEILING MIDLINE

    Navagio

    FDA UDI
    Kalitec Direct LLC·B07330K1100080·Tray Insert

    NIDO Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07315K1100080·Tray Insert

    Cosmolock

    FDA UDI
    Kalitec Direct LLC·B07311K1100080·Tray Insert 1, Cosmolock, Arcamed

    TiWAVE L Lumbar Cage System

    FDA UDI
    Kalitec Direct LLC·B07323K1100080·Tray Insert, Level I

    BD PLASTIPAK¿ LUER-LOK¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·March 23, 2022

    MDT Diamond Coated Dental Burs

    FDA UDI
    M.D.T. - MICRO DIAMOND TECHNOLOGIES LTD.·17291046002336·FG Rotary diamond instrument for dental applica...

    MDT Diamond Coated Dental Burs

    FDA UDI
    M.D.T. - MICRO DIAMOND TECHNOLOGIES LTD.·07291046266083·Rotary diamond instrument for dental application

    PIONEER ANTERIOR CERVICAL PLATE MODEL 24-SERIES

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    APPLICATOR TIP/DUAL SPRAYER KIT

    FDA 510(k)
    FDA Class 2 ·General Hospital

    BD PLASTIPAK¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON, S.A.·Product code FMF·February 16, 2023

    STYLE 68 SALINE FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FWM·October 15, 2025

    BD PRESET¿ ARTERIAL BLOOD COLLECTION SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·June 7, 2024

    BD PRESET¿ ARTERIAL BLOOD COLLECTION SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·November 22, 2024

    QUATTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 10, 2013

    ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code LXH·June 1, 2011