BEUDAMED
    41 results · 21ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    HARDYDISK, KANAMYCIN, 30MCG

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950016532·CURETTE BONE #9 D/E 7-1/4" 18.5CM TIP SIZE APPR...

    Affiniti

    FDA UDI
    TORNIER, INC.·00846832024421·PEGGED GLENOID TRIAL

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092128503·Zimmer® TSV-compatible 4.5mm Digital Analog

    SILVERVENT

    FDA UDI
    Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948000184·SILVERVENT 2 IC, SIZE 3

    SR Facebow

    FDA UDI
    ORMCO CORPORATION·00889989023145·Facebow LONG SZ 3 .044 DIA.

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092134658·Zimmer® TSV-compatible 4.5mm Digital Analog (25...

    Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092134641·Zimmer® TSV-compatible 4.5mm Digital Analog (10...

    HEYER-SCHULTE GEL OVAL BREAST IMPLANT

    FDA Adverse Event
    V. MUELLER DIV. BAXTER HEALTHCARE CORP.·Product code FTR·December 22, 1993

    FlowLogic Agile

    FDA UDI
    SONENDO, INC.·00810209420048·FlowLogic Agile Shaping File 10/.06, 21mm

    Valeo Spacer System

    FDA UDI
    SINTX Technologies, Inc.·M555316000203·Tray 1, Phantom Plus PLIF, TLIF System Case 2

    FRIENDLY LIGHT ER:YAG PULSED LASER

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

    TORNIER TOTAL ELBOW PROSTHESIS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BD SEDI-40

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JPH·November 2, 2020

    BD SEDI-40

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·November 25, 2020

    EXPRESS BILIARY SD MONORAIL PREMOUNTED STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code FGE·June 8, 2007

    12.6CM TAPERED ATTACHEMENT, BLACK MAX

    FDA Adverse Event
    Malfunction ·THE ANSPACH EFFORT, INC.·Product code GFF·February 14, 2013

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·February 18, 2011

    Leksell Gamma Knife. Leksell Gamma Knife is a teletherapy device indicated for use in the stereotactic irradiation of intracranial structures

    FDA Recall
    Terminated ·Elekta, Inc.·Product code IWB·October 1, 2007

    HERO GRAFT

    FDA Adverse Event
    Death ·CRYOLIFE, INC.·Product code DSY·October 15, 2015