BEUDAMED
    26 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 ×

    OPTI CCA-TS2

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TALOS® IBF

    FDA UDI
    MEDITECH SPINE, LLC·B16711311260·

    Ardis®

    FDA UDI
    ZIMMER SPINE, INC.·00889024333871·

    Ardis®

    FDA UDI
    ZIMMER SPINE, INC.·00889024334601·

    Yellowstone

    FDA UDI
    SUMMIT SPINE LLC·B587P13112670·13mm PLIF Implant 11mm Wide 26mm Length, 7 deg ...

    3.5MM CORTEX SCREW SELF-TAPPING 55MM

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code HWC·January 26, 2017

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·July 25, 2018

    PONTIS SUTURES AND SUTURE ANCHORS WITH OPTIONAL CRIMPS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ACRYLIC HERBST APPLIANCE

    FDA 510(k)
    FDA Class 2 ·Dental

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·November 18, 2015

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·June 7, 2018

    MAGEC® SPINAL BRACING AND DISTRACTION SYSTEM

    FDA Adverse Event
    Injury ·NUVASIVE SPECIALIZED ORTHOPEDICS, INC.·Product code PGN·November 1, 2016

    DIGITAL RADIOGRAPHY CXDI

    FDA Adverse Event
    Malfunction ·CANON, INC.·Product code MQB·December 22, 2019

    DIGITAL RADIOGRAPHY CXDI

    FDA Adverse Event
    Malfunction ·CANON, INC.·Product code MQB·December 22, 2019

    DIGITAL RADIOGRAPHY CXDI

    FDA Adverse Event
    Malfunction ·CANON, INC.·Product code MQB·December 22, 2019

    3.5MM CORTEX SCREW SELF-TAPPING 16MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 6, 2016

    3.5MM CORTEX SCREW SELF-TAPPING 14MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·January 6, 2016

    UNKNOWN

    FDA Adverse Event
    Injury ·UNK·Product code FTL·May 22, 2013

    COLLEAGUE P1.7

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 16, 2011

    PFC SIGMA C/R PORT FE TD SZ 2.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code JWH·August 20, 2008