BEUDAMED
    204 results · 30ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    NEUROLUMEN PN-1000

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    PRINCETON

    FDA UDI
    Princeton Medical Group, Inc.·00810158214897·UTERINE DILATOR HEGAR DOUBLE ENDED 25/26MMØ

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707011095·CALIBRA 1ST MOL BANDS W/G8025-02 n.UR 25

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694043151·2.0mm, Locking Reconstruction Plate, 18 Hole, S...

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587L142025120·14mm H x 20mm W x 25mm L XLIF Trial 12 degree L...

    TALOS®-A

    FDA UDI
    SpineArt SA·07640375237842·TALOS®-A (HA) PEEK PLANAR, SYMMETRIC IBFD D26 ...

    TALOS° HA PEEK IBF

    FDA UDI
    MEDITECH SPINE, LLC·B167321420250·

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 3, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 10, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 11, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·October 11, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·September 11, 2019

    COMBAT READY CLAMP

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MODIFICATION TO CD HORIZON SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    CD HORIZON® SPINAL SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC SOFAMOR DANEK·Product code KWP·May 4, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWP·July 8, 2019

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MDT SOFAMOR DANEK USA, INC.·Product code KWP·October 30, 2019