BEUDAMED
    24 results · 24ms · 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 ×

    PMT Facet Fixation System, Lumbar (PMT FFS-LX)

    FDA 510(k)
    FDA Unclassified ·Unknown

    LoFric® Hydro-Kit™

    FDA UDI
    Wellspect AB·07392532142659·Single Use Urinary Catheter LoFric Hydro-Kit Ne...

    Restore

    FDA UDI
    KEYSTONE DENTAL, INC.·D768L23084004K0·COC Abutment

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981158743·Lateral Implant, 23mm x 8mm x 40mm, 0 Deg

    Regatta Lateral System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981162085·Lateral Implant, 23mm x 8mm x 40mm, 10 Deg

    SMARTBUILDER SYSTEM (SB1)

    FDA 510(k)
    FDA Class 2 ·Dental

    MODIFICATION TO HORIZON SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Vu aPod™ - L

    FDA UDI
    Seaspine Orthopedics Corporation·10889981046620·LATERAL IMPLANT, WIDE, LORDOTIC, 8mm X 23mm X 4...

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDIC, INC.·Product code KWP·March 15, 2011

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·September 26, 2016

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·July 26, 2016

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·September 11, 2017

    APPLIANCE, FIXATION, SPINAL INTERLAMINAL

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·October 25, 2017

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·April 4, 2016

    LONG NAIL KIT R1.5, LEFT 10X260MM X 125

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·June 16, 2010

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·WARSAW ORTHOPEDICS·Product code KWP·April 6, 2017

    PINNACLE SECTOR II CUP 58MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·November 6, 2014

    HOMECHOICE AUTOMATED PD SET W/CASSETTE 4-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·November 17, 2008

    GLUCOSE MONITORING SYS/KIT

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2013

    CD HORIZON SPINAL SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·February 7, 2020