BEUDAMED
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    StrokeViewer Perfusion

    FDA 510(k)
    FDA Class 2 ·Radiology

    BD BBL™ Sensi-Disc™ Streptomycin - 50 µg

    FDA UDI
    BECTON, DICKINSON AND COMPANY·00382902315704·BD BBL™ Sensi-Disc™ Streptomycin - 50 µg

    devemed

    FDA UDI
    devemed GmbH·04061644020874·Suture and membrane tweezers, micro I = 1.6 mm,...

    PF4 Enhanced assay

    FDA 510(k)
    FDA Class 2 ·Hematology

    ORTHOVISION

    FDA 510(k)
    FDA Class 2 ·Radiology

    Reicodent

    FDA UDI
    devemed GmbH·04061644031580·Suture and membrane tweezers,micro I = 1,3 mm, ...

    COMPREHENSIVE REVERSE SHOULDER TITANIUM GLENOSPHERE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 4, 2024

    COMPREHENSIVE REVERSE SHOULDER HUMERAL TRAY WITH LOCKING RING

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 4, 2024

    COMPREHENSIVE REVERSE SHOULDER GLENOSHERE MINI BASEPLATE WITH TAPER ADAPTER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 4, 2024

    COMPREHENSIVE REVERSE SHOULDER HUMERAL BEARING ARCOMXL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 4, 2024

    COMPREHENSIVE REVERSE SHOULDER PRIMARY SHOULDER STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 4, 2024

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Death ·W.L. GORE & ASSOCIATES·Product code MIH·November 14, 2008

    SM204 M-SERIES W/BIG WHEEL

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FPO·July 22, 2011

    DEXTRUS 4137

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·July 17, 2013

    COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·May 29, 2024

    COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·May 29, 2024

    COMPREHENSIVE REVERSE SHOULDER CENTRAL SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·May 29, 2024

    COMPREHENSIVE REVERSE SHOULDER FIXED LOCKING SCREW

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·May 29, 2024

    MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

    MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142515, K153343, K173592, K202014, K231560.

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025