BEUDAMED
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    SCRIPPSYSTEM C4 RID KIT

    FDA 510(k)
    FDA Class 2 ·Immunology

    n.a.

    FDA UDI
    Karl Storz GmbH & Co. KG·04048551203828·Needle, Tonsil, straight, long

    NA

    FDA UDI
    LANCER ORTHODONTICS, INC.·00817573022977·ADHESIVE-FORMULA 2 PUSH SYRINGE KIT

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756016988·BUCKS TRACTION

    InTess Lumbar Cage

    FDA UDI
    Kalitec Direct LLC·B07312K0105020·Implant Inserter, 14-16mm, Sleeved

    MODEL THERMO TEK QUICKCARE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TRIPLEX ER. YAG / ND: YAG SYSTEM

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

    M2A MAGNUM MODULAR HD COCR DIA 40MM

    FDA Adverse Event
    Injury ·BIOMET UK LTD.·Product code KWA·May 14, 2014

    CAPSURE Z NOVUS

    FDA Adverse Event
    Malfunction ·MPRI·Product code DTB·October 31, 2012

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 20, 2010

    GALAXY G3 MINI 2MM X 6CM

    FDA Adverse Event
    Malfunction ·MEDOS INTERNATIONAL SARL·Product code KRD·October 6, 2022

    Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010; CD3281-40Q/100056770; CD3297-40/100056933

    FDA Enforcement
    Class II ·Terminated·St Jude Medical Inc.·July 4, 2018