BEUDAMED
    41 results · 23ms · 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 ×

    MECTALIF TRANSFORAMINAL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Graft Integration

    FDA UDI
    Nuvasive, Inc.·00887517243560·Graft Integration Pusher, Graft

    ACE

    FDA UDI
    ACE SURGICAL SUPPLY CO., INC.·00614950010837·ELEVATOR PERIOSTEAL FREER #15 CURVED 8" 20CM

    SchureMed

    FDA UDI
    SCHUERCH CORPORATION·00810057372186·Finger Trap Medium

    LEONE SPA

    FDA UDI
    LEONE SPA·08033707008866·CALIBRA 1ST MOLAR BANDS n.UR 24

    OptiMesh Multiplanar Expandable Interbody Fusion System

    FDA UDI
    SPINEOLOGY INC.·M7403120024·Portal Impactor

    Ø8.0 x 120mm x 24mm CANNULATED PARTIAL THREAD

    FDA UDI
    Osteocentric Technologies, Inc.·00816950027314·Ø8.0 x 120mm x 24mm CANNULATED PARTIAL THREAD

    Ø7.0 x 24mm x 120mm CANNULATED PARTIAL THREAD SCREW

    FDA UDI
    Osteocentric Technologies, Inc.·00816950026836·Ø7.0 x 24mm x 120mm CANNULATED PARTIAL THREAD S...

    NA

    FDA UDI
    STRYKER CORPORATION·04546540992550·4.0mm Cornerstone

    CARIS MINITOME BIOPSY INSTRUMENT

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    TECO DIAGNOSTICS UTI DETECTION STRIPS

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·ACTIVL ARTIFICIAL DISC

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code MJO·October 26, 2016

    PROSTHESIS, INTERVERTEBRAL DISC

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code MJO·October 26, 2016

    Prosthesis, Intervertebral Disc

    FDA Pre-Market Approval
    FDA Class 3 ·Aesculap activL Artificial Disc