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    FORAMATRON V, MODEL D680

    FDA 510(k)
    FDA Unclassified ·Unknown

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092002195·artVeneer life lower posteriors, M, BL4

    CRANIAL DRILL

    FDA 510(k)
    FDA Class 2 ·Neurology

    PIPER

    FDA 510(k)
    FDA Class 2 ·Radiology

    MESHGRAFT™

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024372542·

    MeshgraftTM II Tissue Expansion System

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024372566·3 TO 1 DERMACARRIER

    MESHGRAFT™

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024372535·

    MeshgraftTM II Tissue Expansion System

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024372580·9 TO 1 DERMACARRIER

    MeshgraftTM II Tissue Expansion System

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024372559·1.5 TO 1 DERMACARRIER

    MESHGRAFT™

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024372597·

    MESHGRAFT™

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024372528·

    MeshgraftTM II Tissue Expansion System

    FDA UDI
    ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024372573·6 TO 1 DERMACARRIER

    MAMMARY PROSTHESIS

    FDA Adverse Event
    MCGHAN MEDICAL CORP.·Product code FTR·May 24, 1994

    ASR ACETABULAR CUPS 58

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 13, 2013

    DURALOC OPTION CUP 60MM

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD.·Product code LPH·February 18, 2011

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL MANUFACTURING CORPORATION·Product code MVK·July 3, 2014

    MESHGRAFT II COMPLETE

    FDA Adverse Event
    Injury ·ZIMMER SURGICAL, INC.·Product code FZW·June 14, 2019

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·July 20, 2011

    Zimmer Dermacarriers II skin graft carriers, 9 to 1 dermacarrier, Rx, latex free, sterile, Qty 1, Zimmer, Dover, Ohio; REF 00-2195-015-00. Single use device for use during skin grafting procedures.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code FZW·April 3, 2008

    Zimmer Dermacarriers II skin graft carriers, 3 to 1 dermacarrier, Rx, latex free, sterile, Qty 1, Zimmer, Dover, Ohio; REF 00-2195-013-00. Single use device for use during skin grafting procedures.

    FDA Recall
    Terminated ·Zimmer Inc.·Product code FZW·April 3, 2008