BEUDAMED
    22 results · 22ms · Sources: EU EUDAMED, US FDA

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    MegaGen Dental Implant Abutment

    FDA 510(k)
    FDA Class 2 ·Dental

    MAS PLIF

    FDA UDI
    Nuvasive, Inc.·00887517444707·MAS PLIF Fixation Rod, 30mm Pre-Bent

    Ophthalmic Scissors

    FDA UDI
    KATENA PRODUCTS, INC.·00841668105221·KATZIN TRANSPLANT SCISSORS LEFT

    Integra® Miltex®

    FDA UDI
    INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780160250·Integra® Miltex® DeBakey Occlusion Clamp, 10-1/...

    Meridian

    FDA UDI
    Seaspine Orthopedics Corporation·10889981247652·No-Profile Interbody, 43mm x 30mm x 20mm, 30 Deg

    ResQPOD ITD 10, Military

    FDA UDI
    Zoll Medical Corporation·00847946028329·RESQPOD ITD 10, MILITARY

    ENDOSKELETON® DPK

    FDA UDI
    TITAN SPINE, LLC·00191375051190·Posterior, MIS Perforated, Inner Tray, Top

    ENDOSKELETON® DPK

    FDA UDI
    TITAN SPINE, LLC·00191375051206·Posterior, MIS Perforated, Inner Tray, Bottom

    ENDOSKELETON® DPK

    FDA UDI
    TITAN SPINE, LLC·00191375051213·Posterior, MIS Perforated, Inner Tray, Top

    ENDOSKELETON® DPK

    FDA UDI
    TITAN SPINE, LLC·00191375051220·Posterior, MIS Perforated, Inner Tray, Bottom

    HYPROCURE SUBTALAR IMPLANT SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    STGC-LORDOTIC

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    JGRKNT 1.0MM MINI 3-0 NDLS

    FDA Adverse Event
    Injury ·BIOMET SPORTS MEDICINE·Product code MBI·October 8, 2015

    GMK TOTAL KNEE SYSTEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·April 17, 2025

    ONETOUCHPING GLUCOSEMGMTSYSTEM

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 10, 2014

    COLLEAGUE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 9, 2011

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 23, 2013

    ANN BLUNT TIP SCREW 4X46MM

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code HSB·September 23, 2025

    ANN BLUNT TIP SCREW 4X46MM

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code HSB·September 23, 2025

    Philips Ingenia Elition X with MR Elastography (MRE). 1. Model Number (REF): 781358. 2. Model Number (REF): 782107. 3. Model Number (REF): 782136. 510(k) Numbers: K213516, K223458, K230972, K232030, K251397, K251808

    FDA Recall
    Open, Classified ·Philips North America·Product code LNH·April 14, 2026