BEUDAMED
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    MODIFICATION TO CD HORIZON SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Safco FG Diamonds

    FDA UDI
    SAFCO DENTAL SUPPLY CO.·D72310210613·FG Diamond 805-012 inverted cone regular 5/pack

    BUSCH®, BNA®

    FDA UDI
    BUSCH & CO. GmbH & Co. KG·D8120210611·Carbide, cylinder round, excavating and fissure...

    2040 Ceramic Brackets

    FDA UDI
    AMERICAN ORTHODONTICS CORPORATION·00190746005541·COSMETIC 20/40 UPPER CEN 022 T=0 A=0 R=0

    SUPERIOR BATH, MODEL 6300

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SURGICAL CONTRA-ANGEL HANDPIECES TYPES WS-56E,WS-75E/KM,WS-92 E/3,SURGICAL STRAIGHT HANDPIECES TYPES, S-9, S-10, S-11

    FDA 510(k)
    FDA Class 1 ·Dental

    SUPERCORE BIOPSY INSTRUMENT WITH CO-AXIAL INTRODUCER NEEDLE

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code KNW·September 22, 2023

    ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·January 10, 2019

    VOYAGER NC CORONARY DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code LOX·September 1, 2010

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK, INC.·Product code MAX·May 9, 2019

    SUPERCORE BIOPSY INSTRUMENT 18GA X 15CM

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code KNW·December 12, 2022

    SUPERCORE BIOPSY INSTRUMENT 18GA X 6CM

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code KNW·August 17, 2023

    SUPERCORE BIOPSY INSTRUMENT 18GA X 9CM

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code KNW·January 31, 2023

    SUPERCORE BIOPSY INSTRUMENT WITH CO-AXIAL INTRODUCER NEEDLE

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code KNW·October 17, 2023

    ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·July 2, 2018

    POLARCATH

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - SAN JOSE·Product code DQY·March 26, 2013

    SPRINT FIDELIS

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·March 16, 2011

    INDURA

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LKK·March 27, 2008

    SUPERCORE BIOPSY INSTRUMENT 18GA X 6CM

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code KNW·October 28, 2021

    SUPERCORE BIOPSY INSTRUMENT 16GA X 15CM

    FDA Adverse Event
    Malfunction ·ARGON MEDICAL DEVICES·Product code KNW·August 9, 2022