BEUDAMED
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    Amvex Vacuum Regulator

    FDA UDI
    OHIO MEDICAL, LLC·00628101502072·VR-LP series, VacReg, Ped Int 3Mode 200mmHg, An...

    Welch Allyn, Inc.

    FDA UDI
    WELCH ALLYN, INC.·00732094328868·H12+ Standard 12-lead digital Holter Recorder -...

    ACUMATCH M-SERIES LPB 12/14 FEMORAL STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AMS APOGEE SYSTEM WITH PC COATED INTEPRO LITE

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTP·October 14, 2015

    NV GXL LINR, NTRL, 36MM ID, GROUP 3 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·October 28, 2024

    AMS APOGEE SYSTEM WITH PC COATED INTEPRO LITE

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTP·June 18, 2015

    AMS MONARC+ SUBFASCIAL HAMMOCK

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS·Product code OTN·October 24, 2014

    CLIP, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·DAVIS & GECK CARIBE LTD·Product code FZP·October 26, 2018

    M-SERIES LPB NECK, HI OFFSET +10

    FDA Adverse Event
    Malfunction ·EXACTECH, INC.·Product code LZO·July 25, 2014

    LPB M-SERIES NECK HI OFFSET -5

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·August 18, 2017

    AMS ELEVATE POSTERIOR PROLAPSE REPAIR SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS·Product code OTP·December 17, 2014

    AMS ELEVATE POSTERIOR PROLAPSE REPAIR SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code OTP·August 29, 2014

    ACUMATCH M-SERIES LPB NECK SEGMENT, LOW OFFSET

    FDA Adverse Event
    Other ·EXACTECH INC.·Product code LZO·March 24, 2014

    ACUMATCH M-SERIES NECK SEGMENT, LPB¿, HIGH OFFSET

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code LPH·July 25, 2017

    Vena Tech LP Vena Cava Filter System, Item No/REF. 05010024, Model No: 40DLP, B Braun. Manufacturer: B. Braun Medical 204, avenue du Marechal Juin BP 331 92107 Boulogne Cedex , France. (The VenaTech LP vena cava filter is pre-loaded in a syringe (cartridge) and provided as a system with introducer accessories and instructions to accommodate delivery and implantation either via the femoral or jugular approach.)

    FDA Recall
    Terminated ·B. Braun Interventional Systems·Product code DTK·October 30, 2007

    SEPRAFILM

    FDA Adverse Event
    Injury ·GENZYME CORPORATION(FRAMINGHAM)·Product code MCN·December 24, 2018

    SEPRAFILM

    FDA Adverse Event
    Death ·GENZYME CORPORATION(FRAMINGHAM)·Product code MCN·September 10, 2019

    SEPRAFILM

    FDA Adverse Event
    Injury ·GENZYME CORPORATION(FRAMINGHAM)·Product code MCN·December 27, 2019

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014

    UNKNOWN OPTEASE VENA CAVA FILTER

    FDA Adverse Event
    Injury ·CORDIS CORPORATION·Product code DTK·November 3, 2014