BEUDAMED
    23 results · 24ms · Sources: EU EUDAMED, US FDA

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    IdentiTi™ Porous Ti Interbody System, IdentiTi™ NanoTec™ Interbody System, Transcend™ PEEK Interbody System, Transcend™ NanoTec™ Interbody System, IdentiTi™ ALIF Standalone Interbody System, IdentiTi™ NanoTec™ ALIF Standalone Interbody System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    HEALIX ADVANCE PEEK ANCHOR w/DYNACORD

    FDA UDI
    Medos International Sàrl·10886705029426·HEALIX ADVANCE PEEK ANCHOR w/DYNACORD PEEK Anch...

    FAC-4 - Class B 21 White Cap - 4 Shelf Cabinet

    FDA UDI
    Certified Safety Manufacturing, Inc.·00766588620282·FAC-4 - Class B 21 White Cap - 4 Shelf Cabinet

    VX-400 TOPICAL HYPERBARIC OXYGEN CHAMBER

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

    AURICAL HIT

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    SMARTEZ

    FDA Adverse Event
    Malfunction ·EPIC INTERNATIONAL(THAILAND) COMPANY LIMITED·Product code MEB·May 5, 2026

    SMARTEZ PUMP

    FDA Adverse Event
    Malfunction ·EPIC INTERNATIONAL(THAILAND) COMPANY LIMITED·Product code MEB·May 5, 2026

    CADD MEDICATION CASSETTE RESERVIOR, 50ML

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·October 16, 2023

    CADD MEDICATION CASSETTE RESERVIOR, 50ML

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·October 16, 2023

    LACTO 1.5 2X2 SQUARE PLATE

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·October 6, 2025

    INZII RETRIEVAL SYSTEM

    FDA Adverse Event
    Malfunction ·APPLIED MEDICAL RESOURCES·Product code GCJ·March 5, 2026

    PUMP MMT-712LNAS PRDGM INS SK EN US LN

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·November 3, 2008

    RESERVOIR 3ML

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS MED-REL·Product code FRN·August 17, 2011

    ADVANCE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·July 3, 2013

    LSL Healthcare Wound Closure Tray, Model/Catalog Number: 7554

    FDA Enforcement
    Class II ·Ongoing·LSL Healthcare Inc.·April 29, 2026

    MW5072599

    FDA Adverse Event
    Injury ·October 4, 2017

    4.5HLX ADV PK ANC-DYNA STR/BL

    FDA Adverse Event
    Injury ·MEDOS INTERNATIONAL SàRL·Product code MBI·November 15, 2018

    ANN BLUNT TIP SCREW 4X52MM

    FDA Adverse Event
    Malfunction ·ZIMMER GMBH·Product code HSB·May 30, 2024

    BLUNT TIP SCREW, ÿ 4X48MM

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code HSB·April 29, 2025

    JUGGERSTITCH CURVED IMPLANT

    FDA Adverse Event
    Malfunction ·ZIMMER BIOMET, INC.·Product code MBI·March 12, 2024