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

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    Body System

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16741824400·

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B1674182440060·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X1824400·18mm H x 24mm W x 40mm L x 0 degrees XLIF

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00842528127926·2.4 X 40mm Cannulated Headed Screw, T7

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X18244080·18mm H x 24mm W x 40mm L x 8 degrees XLIF

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L182440120·18mm H x 24mm W x 40mm L XLIF Trial 12 degree L...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587X182440120·18mm H x 24mm W x 40mm L x 12 degrees XLIF

    RESTORELLE L

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

    AB DENTAL DEVICES IMPLANTS AND ACCESSORIES

    FDA 510(k)
    FDA Class 2 ·Dental

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021