BEUDAMED
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    JAS Diagnostics

    FDA UDI
    DREW SCIENTIFIC, INC.·00817274022245·IRON STANDARD BULK

    Roscoe Medical

    FDA UDI
    COMPASS HEALTH BRANDS CORP.·00092237603499·Compressor intake filter

    HEARING AID, DM IROS

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

    HEARING AID, DM IROS DIRECTIONAL

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

    FLUOROSCOPIC X-RAY

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·October 24, 2007

    9600+

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS INC·Product code JAA·November 7, 2007

    TIME MACHINE/ELECTRICAL STIMULATOR

    FDA Adverse Event
    CONNIE STEVENS FOREVER SPRING BEAUTY SYSTEM·Product code IRO·February 1, 1994

    VIBRACARE PERCUSSOR

    FDA Adverse Event
    Injury ·GENERAL PHYSIOTHERAPY, INC.·Product code IRO·December 18, 1996

    D ARSENVAL

    FDA Adverse Event
    Malfunction ·SKINRECHARGE LLC·Product code IRO·February 13, 2009

    UNK

    FDA Adverse Event
    Other ·*·Product code IRO·January 22, 2009

    QUICKIE 2 WHEELCHAIR

    FDA Adverse Event
    Malfunction ·SUNRISE MEDICAL MPD·Product code IRO·December 16, 1998

    S-ROM*FRAME,TRIANGLE MILLER

    FDA Adverse Event
    Malfunction ·DEPUY ORTHOPAEDICS, INC.·Product code LXH·March 18, 2014

    GN RESOUND

    FDA Adverse Event
    Injury ·GN HEARING A/S·Product code OSM·June 1, 2022

    ALINITY M SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code OOI·September 24, 2024

    GORE-TEX® CARDIOVASCULAR PATCH

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code DXZ·October 10, 2018

    ALINITY M SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MOLECULAR, INC.·Product code OOI·September 24, 2024

    CRILE FCPS 5-1/2 CVD SATIN

    FDA Adverse Event
    Malfunction ·INTEGRA YORK, PA INC.·Product code HRQ·November 26, 2018

    IRON GEN.2

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JIY·March 21, 2017

    LCP PROXIMAL LATERAL TIBIA PLATE 7 HOLES/180MM-RIGHT

    FDA Adverse Event
    Injury ·SYNTHES GRENCHEN·Product code HRS·February 12, 2015

    USA-002 Rev A brochure is a two sided tri-fold printed marketing brochure describing the approved labeling indications for use, precautions and general operational information of the Exer-Rest device, Models AT3800 and AT4700. Brochure: "EXER-REST***A patented, FDA registered, Acceleration Therapeutics device delivering Whole Body Periodic Acceleration to the user for symptomatic relief of a wide range of complaints***Whole Body Periodic Acceleration (WBPA)***WBPA is accomplished utilizing the Ever-Rest device to move the body repetitively head to foot at approximately 140 times a minute. This repetitive motion adds pulses to your natural vascular pulse with each acceleration and deceleration of the body. These additional pulses act on the inner lining of blood vessels (endothelium) throughout the body, a process called pulsatile shear stress, to promote the release of beneficial substances (mediators). These mediators, such as nitric oxide, provide a wide range of health benefits that originate from the user's own body.***Nitric Oxide (NO) is released from endothelial cells that line the arterial walls. NO signals vascular smooth muscle to relax, thereby increasing blood flow throughout the circulation.***NiMS 4400 Biscayne Blvd., Miami, FL 33137 P 305.575.4200 F 305357534201***[email protected] www.nims-inc.com***NIMS, Acceleration Therapeutics and Exer-Rest are registered trademarks of Non-Invasive Monitoring Systems, Inc.***USA-002 Rev A***" Printed marketing brochure

    FDA Recall
    Terminated ·Non-Invasive Monitoring Systems, Inc.·Product code IRO·May 7, 2012