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    DAHLBERG HEARING AID MODEL MEH

    FDA 510(k)
    FDA Class 1 ·Ear, Nose, Throat

    RETRACTOR U OF M EH-LG

    FDA UDI
    W.H. Holden, Inc.·D928105530EH0·

    MEHS-COMPOSIX

    FDA Adverse Event
    Injury ·DAVOL INC·Product code FTL·January 4, 2012

    MEH-COMPOSIX KUGEL

    FDA Adverse Event
    Other ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·December 13, 2007

    MEHS- COMPOSIX KUGEL

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·January 17, 2008

    BARD FLAT MESH

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·March 8, 2022

    BARD FLAT MESH

    FDA Adverse Event
    Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·June 22, 2023

    UNK WOMEN'S HEALTH MEHS PRODUCT

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON)·Product code OTP·November 20, 2013

    PARIETEX

    FDA Adverse Event
    Injury ·SOFRADIM PRODUCTION SAS·Product code FTL·April 22, 2022

    PROSTHESIS, HIP, SEMI-CONSTRAINED, UNCEMENTED, METAL/POLYMER, NON-POROUS, CALICU

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code MEH·October 15, 2025

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code GBO·February 2, 2023

    UNKNOWN

    FDA Adverse Event
    Injury ·COOK INC·Product code GBO·February 2, 2023

    SECUR-FIT HA HIP STEM #8

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS·Product code MEH·February 5, 2010

    SECUR-FIT HA HIP STEM #10

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS·Product code MEH·February 5, 2010

    TRIDENT PSL SHELL SIZE 58

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS CORK STRYKER ORTHOPAEDICS·Product code MEH·February 5, 2010

    SUPER SECUR FIT PLUS

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK, STRYKER ORTHOPAEDICS·Product code MEH·February 5, 2010

    ULTRATHANE RING BILIARY DUCT DRAINAGE CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code GCA·November 15, 2017

    RESTORELLE Y

    FDA Adverse Event
    Injury ·COLOPLAST A/S·Product code OTO·July 3, 2020

    GYNECARE TVT DEVICE

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·February 7, 2020

    TRIDENT 0 DEG X3 INSERT 36MM ID

    FDA Adverse Event
    Malfunction ·STRYKER ORHTOPAEDICS·Product code MEH·February 5, 2010