BEUDAMED
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    VIMEDIC SYSTEM TM

    FDA 510(k)
    FDA Class 1 ·Dental

    Preat

    FDA UDI
    Preat Corporation·00842092172575·2.5mm Retention Caps--Green (6-Pack)

    Convaid

    FDA UDI
    CONVAID PRODUCTS, INC.·00840117408517·

    Convaid

    FDA UDI
    CONVAID PRODUCTS, INC.·10840117400907·

    Marina Medical

    FDA UDI
    MARINA MEDICAL INSTRUMENTS, INC.·00840306809705·Infusion Handle with on/off control valve

    COOLTOUCH MODELS LC215 AND COOLLIPO

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PM 2002 PROLINE/AEC

    FDA 510(k)
    FDA Class 2 ·Dental

    PFC TOTAL CONDULAR 3 REINFORCED TIBIAL INSERT

    FDA Adverse Event
    Injury ·JOHNSON & JOHNSON PROFESSIONALS, INC.·Product code HSH·October 30, 1997

    SYNCHROMED

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·May 8, 2014

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·October 12, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·August 29, 2007

    SMR CEMENTLESS FINNED STEM

    FDA Adverse Event
    Injury ·LIMACORPORATE S.P.A.·Product code HSD·June 18, 2019

    Product Label - ACUSON Sequoia *** Power Input: 100-240V~, 13.0-5.4A, 50-60Hz *** (240)11148775 Model User Manual states - ACUSON Sequoia Diagnostic Ultrasound Systems

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc.·April 7, 2021

    ACUSON Sequoia Ultrasound Imaging System with Software Version VA25A/B

    FDA Enforcement
    Class II ·Ongoing·Siemens Medical Solutions USA, Inc.·February 9, 2022