BEUDAMED
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    ELEOS Limb Salvage System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    XENMATRIX

    FDA UDI
    Davol Inc.·00801741031410·XenMatrix Surgical Graft, 15 cm x 20 cm (5.9" x...

    Mouthpiece, Disposable, One-Way Valve

    FDA UDI
    A-M SYSTEMS, LLC·00817081023435·Mouthpiece, Disposable, One-Way Valve

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528126936·ExtremiFix Mini, 2.0mm Screw Module

    Symmetry Crafoord (Coller)

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00887482056288·Symmetry® Forceps, Crafoord Coller Artery, Deli...

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167311615200·

    TALOS® HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321615200·

    VIPER SPINE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ENSEAL TISSUE SEALING DEVICES MODEL: NSEAL514H-535H, NSEAL514RH-535RH

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

    HAMILTON MEDICAL AG

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·December 1, 2023

    HAMILTON MEDICAL AG

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·November 28, 2023

    HAMILTON-C1

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·November 21, 2023

    HAMILTON MEDICAL AG

    FDA Adverse Event
    Malfunction ·HAMILTON MEDICAL AG·Product code CBK·December 1, 2023

    HNM Medical

    FDA UDI
    HNM STAINLESS, LLC.·00842962111499·CRAFOORD COLLER FORCEPS, 8", CVD

    STERIS

    FDA Adverse Event
    Malfunction ·VILEX·Product code HTY·April 6, 2005

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·February 12, 2019

    INDIGO SYSTEM SEPARATOR D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·April 18, 2018

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·May 29, 2019

    INDIGO SYSTEM CATD ASPIRATION CATHETER

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·January 17, 2020

    INDIGO SYSTEM ASPIRATION CATHETER D

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code DXE·December 7, 2018