BEUDAMED
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    HAND HELD PHEUMATIC POWERED (DISPOSABLE) NEBULIZER

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88700271·Max. 2. Molar band W-Fit right 27

    Trimline

    FDA UDI
    ORMCO CORPORATION·00889989052008·UPPER LEFT SECOND MOLAR TRIMLINE BAND SIZE 27

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707033066·WEB 1ST MOLAR BANDS n.LL 27

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88700270101·Max. 2. Molar band W-Fit right 27

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867313835·Depth Device, 1.4 / 1.6mm

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88700270501·Max. 2. Molar band W-Fit right 27

    N.A.

    FDA UDI
    Forestadent Bernhard Förster GmbH·EFOR88700270051·Max. 2. Molar band W-Fit right 27

    Arthrex®

    FDA UDI
    ARTHREX, INC.·00888867313842·Depth Device, 1.4 / 1.6mm, Pin Assembly

    POWDERED (WHITE) VINYL PATIENT EXAMINATION

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ACCELERATOR, LINEAR, MED.

    FDA 510(k)
    FDA Class 2 ·Radiology

    VAL SCREW, TI, 1.6 X 9MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·December 21, 2020

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·December 21, 2020

    VAL SCREW, TI, 1.6 X 10MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·December 21, 2020

    DEPTH DEVICE, 1.4 / 1.6MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·January 17, 2024

    DEPTH DEVICE, 2.0 / 2.4MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·January 17, 2024

    DEPTH DEVICE, 1.4 / 1.6MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·November 15, 2023

    DEPTH DEVICE, 2.0 / 2.4MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·November 15, 2023

    CORTOSS 10CC OUS

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOBIOLOGICS-MALVERN·Product code NDN·June 12, 2014

    FOGARTY ARTERIAL EMBOLECTOMY CATHETER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES PR·Product code DXE·October 15, 2010