BEUDAMED
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    FDA 510(k)
    FDA Class 2 ·General Hospital

    NA

    FDA UDI
    Fehling Instruments GmbH & Co. KG·04058749072303·POLYTEL Titanium retracting blade, pointed, 105...

    GoldenDent

    FDA UDI
    GoldenDent·00850011211878·Non Serrated Tissue Membrane Force

    CART 9734056 S7 STAFF SHRT 100-120V INTL

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC·Product code HAW·April 11, 2022

    MRI

    FDA Adverse Event
    Death ·Product code LNH·July 13, 2016

    SURGICEL ABSORBABLE HEMOSTAT UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code LMG·November 17, 2020

    TempaDOT

    FDA UDI
    MEDICAL INDICATORS INC·00016944301035·TempaDOT F Non-Sterile single use Clinical ther...

    TempaDOT

    FDA UDI
    MEDICAL INDICATORS INC·00016944301134·TempaDOT F Non-Sterile Single use Clinical Ther...

    DURAGEN-UNKNOWN PRODUCT ID

    FDA Adverse Event
    Injury ·INTEGRA LIFESCIENCES CORPORATION·Product code GXQ·August 24, 2018

    STEALTHSTATION® S7

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC·Product code HAW·July 17, 2019

    ADAPTOR,1,P417,S417,1/4" N,SF

    FDA UDI
    CURBELL MEDICAL PRODUCTS, INC.·00840828118385·ADAPTOR,1,P417,S417,1/4" N,SF

    CoolSculpting Elite Card, Solo,NSF, ZA20-002

    FDA UDI
    Zeltiq Aesthetics, Inc.·00816417022470·CoolSculpting Elite Card, Solo,NSF, ZA20-002

    ELEMENT MC INICELL, PF 4,5, E 4,2, L 11,0

    FDA Adverse Event
    Injury ·THOMMEN MEDICAL AG·Product code DZE·September 25, 2018

    SOCLEAN 2

    FDA Adverse Event
    Injury ·SOCLEAN, INC.·Product code LRJ·December 17, 2021

    LINEAGE(R) TRANSCEND(R) METAL ACETABULAR LINER

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDL·October 4, 2007

    SOCLEAN 2

    FDA Adverse Event
    Injury ·SOCLEAN, INC.·Product code LRJ·December 7, 2021

    LINEAGE(R) TRANSCEND(R) SUPERFINISHED FEMORAL HEAD

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDL·October 4, 2007

    TRANSCEND(R) QUADRANT SHELL

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code KWB·October 4, 2007

    UNK - SCREWS: 6.5 MM AND 7.3 MM CANNULATED

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·March 23, 2020

    UNK - SCREWS: 6.5 MM AND 7.3 MM CANNULATED

    FDA Adverse Event
    Injury ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HWC·March 23, 2020