BEUDAMED
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    OrthoButton CL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ABC

    FDA UDI
    Conmed Corporation·10653405003885·ABC PROBE 5 MM FOOTSWITCHING PROBE

    MECTALIF ANTERIOR MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X35 ENHANC

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code OVD·July 5, 2019

    SCOUTPRO 8F, MODELS 342 262; HEMOSTATIC VALVE, MODELS 345 968; HOOK GUIDING CATHETER, MODELS 342 263; MULTI-PURPOSE H

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MAHE PERFECT SPINE- PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    LAP PROBE,ABC,5 MM,F/S,DISP

    FDA Adverse Event
    Injury ·Product code GEI·August 26, 2021

    ABC PROBE REF 160655 5 mm Footswitching Probe, QTY: 1 STERILE CONMED CORPORATION 525 French Rd, Utica, NY 13501 ASSEMBLED IN MEXICO ABC PROBE REF 160655 5 mm Footswitching Probe, QTY: 10 STERILE CONMED CORPORATION 525 FRENCH RD UTICA, NY 13205 ASSEMBLED IN MEXICO Usage: Electrosurgical handpiece for use as monopolar electrosurgical accessory in conjunction with CONMED electrosurgical units equipped with argon beam coagulation.

    FDA Recall
    Terminated ·ConMed Electrosurgery·Product code GEI·December 18, 2008

    CAPSUREFIX MRI SURESCAN

    FDA Adverse Event
    Malfunction ·MPRI·Product code NVN·October 10, 2014

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code ILS·June 10, 2013

    ITREL 3

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·July 7, 2011

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X35 ENHANCED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·December 16, 2022

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X25 ENHANCED

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·April 17, 2019

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X35 ENHANCED (DOUBLE PACKAGING)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code OVD·September 3, 2019

    MECTALIF ANTERIOR STAND-ALONE PLATE FLUSH H.12 MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·March 29, 2018

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X35 ENHANCED (DOUBLE PACKAGING)

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code OVD·September 2, 2019

    MECTALIF ANTERIOR STAND-ALONE SCREW DIAM.5X30 ENHANCED

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code OVD·September 20, 2018

    MECTALIF ANTERIOR SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·May 6, 2025

    LAP PROBE,ABC,5 MM,F/S,DISP

    FDA Adverse Event
    Injury ·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·November 1, 2022

    Piston Syringe and Hypodermic Needle, 1 CC TB 28 G X 0.5, 100 per box, 30 boxes/case, 3,000/case

    FDA Enforcement
    Class II ·Terminated·International Medsurg Connection, Inc.·August 16, 2017

    Syringe Bulb, 60 CC 50 pcs per case. The products are used to inject fluids into, or withdraw fluids from the body. They are intended for use in the diagnosis of disease or other conditions or in the cure, mitigation, treatment or prevention of disease, or to affect the structure or any function of the body.

    FDA Enforcement
    Class II ·Terminated·International Medsurg Connection, Inc.·August 16, 2017