BEUDAMED
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    THE BREATHER

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Damon 3MX

    FDA UDI
    ORMCO CORPORATION·00889989002294·L1 and 2R DAMON3 MX 22 -6/2/0

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690191018·AK3 Flat Insert Trial Size 4-6 - 12mm

    ACT ARTIC E1 HIP BRG 28X44MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code LPH·August 8, 2023

    MASK, SURGICAL, DISPOSABLE

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

    ALLEVYN DRESSING CLAIMS CHANGE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DEXTRUS 4137

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVZ·December 16, 2010

    PRECISION XTRA

    FDA Adverse Event
    Malfunction ·Product code NBW·February 5, 2013

    PRECISE SDS SELF EXPANDING

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code FGE·July 18, 2014