BEUDAMED
    16 results · 39ms · 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 ×

    EPICARE-DUO LASER SYSTEM

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

    PRONOVA NONABSORBABLE SUTURE, USP

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

    VASOCOR VASCULAR DIAGNOSTIC CENTER (MODEL 300)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    FEMORAL POSTERIOR AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    STEM EXTENSION STRAIGHT SPLINED UNCEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    FEMORAL DISTAL AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·June 2, 2022

    FEMORAL DISTAL AUGMENT CEMENTED

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    SEE H10 NARRATIVE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    SEE H10 NARRATIVE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    TIBIA FIXED CEMENTED LEFT SIZE D STEM EXTENSION

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JWH·May 16, 2023

    TIBIAL AUGMENT CEMENTED HALF BLOCK

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBH·August 17, 2022

    M2A-38 CUP NON FLARED SZ 54MM

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·May 3, 2013

    NATURALYTE

    FDA Adverse Event
    Injury ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·August 22, 2014

    EON MINI RECHARGEABLE IPG

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION DIVISION·Product code LGW·April 28, 2011