BEUDAMED
    25 results · 23ms · Sources: EU EUDAMED, US FDA

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    TI-MAX PROTRUSIO CAGE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ODYSSEY®

    FDA UDI
    Microport Orthopedics Inc.·M684K00143761·

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001376·artVeneer life upper anteriors, IXL, C3

    3M™ Unitek™

    FDA UDI
    3m do Brasil Ltda.·00652221002211·Unitek(TM) Standard Edgewise Bracket Single U/L...

    Bravo

    FDA UDI
    SUNTECH MEDICAL, INC.·10840935105503·

    DISPOSABLE MICROKERATOME BLADES-PE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    SPECIALTY 42 (HEFILCON A) HYDROPHILIC CONTACT LENS FOR DAILY WEAR, SPECIALTY T-42 TORIC (HEFILCON A) HYDROPHILIC CONTACT

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 24, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 23, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·January 13, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·January 26, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·November 3, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·December 28, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·November 3, 2025

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 15, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 7, 2026

    TUFF IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·June 11, 2025

    LCP 3.5 7HO L98 SST

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HRS·March 13, 2013

    CLIP, IMPLANTABLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·February 25, 2011

    ANIMAS INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·ANIMAS CORP.·Product code LZG·February 20, 2008