BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    LTM-Perforated Surgical Mesh

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

    Oticon

    FDA UDI
    Oticon A/S·05707131281586·NERA2, BTE 13 WL 100 SGR

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100066·TEMPORAL SPECULUM CLOSED WIRE

    Bonding Accessories

    FDA UDI
    TP ORTHODONTICS INC·00192029000236·TPO Blue Etchant Gel

    Ophthalmic Speculum

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100196·MCINTYRE SPECULUM OPEN WIRE

    Scorpio

    FDA UDI
    Howmedica Osteonics Corp.·07613154020232·Posterior Stabilized Tibial Insert

    Sklar

    FDA UDI
    SKLAR CORPORATION·30649111009673·SOLUTION BASIN 9 1/2 QT PK/12

    HNM Women Care

    FDA UDI
    HNM STAINLESS, LLC.·00812171028697·PESSARY, HODGE #9, W/O SUPPORT, 110mm

    RESOUND ENDOSCOPIC ULTRASOUND ASPIRATION NEEDLE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    4.5.* 6.0MM DENTAL IMPLANT AND 6.0*6.0 MM DENTAL IMPLANT

    FDA 510(k)
    FDA Class 2 ·Dental

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·June 12, 2025

    MECHANICAL WALKER, ROLLATOR

    FDA Adverse Event
    UNKNOWN·Product code ITJ·October 8, 2014

    ASR UNI FEMORAL IMPL SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·June 6, 2013

    TI 3-D HEAD FOR TI CLICK'X SCREWS

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code NKB·June 24, 2011