BEUDAMED
    308 results · 34ms · Sources: EU EUDAMED, US FDA

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    Superion Interspinous Spacer

    FDA UDI
    VERTIFLEX, INC.·00884662000222·Superion Interspinous Spacer, 8mm

    Superion Dilator 1, Blunt

    FDA UDI
    VERTIFLEX, INC.·00884662000321·SuperionDilator 1, Blunt

    Superion Mallet

    FDA UDI
    VERTIFLEX, INC.·00884662000208·Superion Mallet

    Superion Inserter

    FDA UDI
    VERTIFLEX, INC.·00884662000130·Superion Inserter

    Superion Interspinous Spacer

    FDA UDI
    VERTIFLEX, INC.·00884662000246·Superion Interspinous Spacer, 10mm

    Superion Grasping Forceps

    FDA UDI
    VERTIFLEX, INC.·00884662000147·Superion Grasping Forceps

    Superion Driver

    FDA UDI
    VERTIFLEX, INC.·00884662000123·Superion Driver

    Superion Interspinous Reamer

    FDA UDI
    VERTIFLEX, INC.·00884662000178·Superion Interspinous Reamer

    Superion Cannula

    FDA UDI
    VERTIFLEX, INC.·00884662000345·Superion Cannula

    Superion Dilator 1

    FDA UDI
    VERTIFLEX, INC.·00884662000369·Superion Dilator 1

    Superion Interspinous Spacer

    FDA UDI
    VERTIFLEX, INC.·00884662000284·Superion Interspinous Spacer, 14mm

    Superion Sterilization Tray

    FDA UDI
    VERTIFLEX, INC.·00884662000185·Superion Sterilization Tray

    Superion Interspinous Spacer

    FDA UDI
    VERTIFLEX, INC.·00884662000307·Superion Interspinous Spacer, 16mm

    Superion Handle

    FDA UDI
    VERTIFLEX, INC.·00884662000352·Superion Handle

    Superion Interspinous Spacer

    FDA UDI
    VERTIFLEX, INC.·00884662000260·Superion Interspinous Spacer, 12mm

    Superion Dilator 2

    FDA UDI
    VERTIFLEX, INC.·00884662000338·Superion Dilator 2

    Superion Retractor

    FDA UDI
    VERTIFLEX, INC.·00884662000192·Superion Retractor

    Superion Interspinous Gauge

    FDA UDI
    VERTIFLEX, INC.·00884662000154·Superion Interspinous Gauge

    SILVERBOLT PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Other ·VERTIFLEX, INC.·Product code NQP·February 3, 2010

    SUPERION INTERSPINOUS SPACER

    FDA Adverse Event
    Injury ·VERTIFLEX INC.·Product code NQO·June 24, 2021