BEUDAMED
    9 results · 19ms · Sources: EU EUDAMED, US FDA

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    uDR Aurora CX

    FDA 510(k)
    FDA Class 2 ·Radiology

    GIBSON HEALTHCARE

    FDA UDI
    BENCO DENTAL SUPPLY CO.·00366975012593·Gibson Healthcare Synthetic Granules, Synthetic...

    NuVasive PEEK Corpectomy System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    REVOLIX AND REVOLIX JR

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

    SPECIFIC DEVICE NOT REPORTED

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWT·August 12, 2024

    RESTORE RECHARGABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·September 8, 2011

    BROVIAC

    FDA Adverse Event
    Malfunction ·C. R. BARD, INC.·Product code FOZ·November 4, 2014

    PEDICSCR MATRIX 5.5 POLYAXIAL Ø5 PREASSM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·July 29, 2013

    ACCOLADE DR SL MRI (Model L311)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025