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

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    Solitaire 4 Revascularization Device

    FDA 510(k)
    FDA Class 2 ·Neurology

    Vanguard® Knee System

    FDA UDI
    Biomet Orthopedics, LLC·00880304270480·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528128206·3.0 X 22mm Cannulated Headed Screw, T10

    MEDICAL GRAPHICS CORP.

    FDA registration
    MEDICAL GRAPHICS CORP.·8 products·🇺🇸 United States

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180538340·LIF Cobb, Straight 22mm, Latching

    CosmoLock Pedicle Screw System

    FDA UDI
    Kalitec Direct LLC·B07311K1430220·Rod Cutter, Table Top

    KIM

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

    PURESLEEP

    FDA 510(k)
    FDA Class 2 ·Dental

    MOTO PARTIAL KNEE ANATOMICAL FEMORAL COMPONENT CEMENTED S5 - LATER

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code HSX·December 16, 2020

    UNKNOWN MEDTRONIC HARDWARE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code KWQ·October 17, 2014

    RESTORE SENSOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·June 21, 2013

    COLLEAGUE PRE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011

    BIOMET CC I-BEAM TRAY 63MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·November 6, 2018

    VANGUARD (TM) DCM TIBIAL BEARING ANTERIOR STABILIZIED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    VANGUARD E1 TIBIAL BEARING 10MMX67MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 6, 2018

    VANGUARD (TM) DCM TIBIAL BEARING ANTERIOR STABILIZIED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

    VNGD CR TIB BRG 10X63/67

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 8, 2018

    SERIES A PAT STD 28 3 PEG

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·August 7, 2018

    Biomet Vanguard CR femoral 57.5 mm left interlok, Sterile, REF 183022, Knee prosthesis component.

    FDA Recall
    Terminated ·Biomet, Inc.·Product code JWH·April 20, 2010

    VANGUARD CR TIBIAL BEARING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·November 6, 2018