BEUDAMED
    140 results · 21ms · Sources: EU EUDAMED, US FDA

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    IdentiTi Porous Ti Interbody System, Transcend PEEK Interbody System, IdentiTi NanoTec Interbody System, Transcend NanoTec Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Sochi

    FDA UDI
    Altus Spine, LLC·00843210167244·Offset Hook, Left, Medium

    ALEUTIAN Interbody Systems

    FDA UDI
    VB Spine LLC·10888857557482·Removal Tool Size 15 x 305 mm

    Atoll

    FDA UDI
    Seaspine Orthopedics Corporation·10889981033842·Offset Hook (left) - medium. The Atoll OCT Spin...

    ECG SERIES ELECTROCARDIOGRAPH

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    AMS LARGE PORE POLYPROPHLENE MESH

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·December 23, 2025

    COLIBRI

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code HWE·October 29, 2014

    ASR UNI FEMORAL IMPLANT SIZE 47

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·August 10, 2011

    TALENT TAA STENT GRAFT

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·July 8, 2013

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·November 21, 2025

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·April 30, 2025

    BEBACK CROSSING CATHETER

    FDA Adverse Event
    Malfunction ·BENTLEY INNOMED GMBH·Product code PDU·March 6, 2025

    MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

    FDA Enforcement
    Class I ·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025

    MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

    COOK CELECT® PLATINUM NAVALIGN FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·May 19, 2022

    COOK CELECT® PLATINUM NAVALIGN FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·May 19, 2022

    COOK CELECT® PLATINUM NAVALIGN FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·May 19, 2022

    COOK CELECT® PLATINUM NAVALIGN FEMORAL VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·May 19, 2022

    COOK CELECT® PLATINUM NAVALIGN UNISET VENA CAVA FILTER SET

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code DTK·May 19, 2022