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

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    VIPER PRIME™ Screws with Fenestrations

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO HEALTH BUDDY APPLIANCE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MEDISSISS REPROCESSEDENT ABLATION WANDS (COBLATORS), MODEL#EIC8872-01

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

    NEXSYS PCS SYSTEM

    FDA Adverse Event
    Malfunction ·HAEMONETICS CORPORATION·Product code GKT·May 12, 2021

    ANK IMPL A9,5 D3,5 MM/L9,5 MM

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·August 28, 2025

    ANK C/X IMPL A9.5/D3.5/L9.5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·March 18, 2025

    ANK IMPL A9,5 D3,5 MM/L9,5 MM

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·October 12, 2023

    ANK IMPL A9,5 D3,5 MM/L9,5 MM

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·August 19, 2025

    COMPETITOR UNKNOWN PRODUCT IMPLANTS

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·November 22, 2023

    ANK C/X IMPL A14/D3.5/L14

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·April 8, 2024

    ANK IMPL A9,5 D3,5 MM/L9,5 MM

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·June 25, 2024

    ANK C/X IMPL A11/D3.5/L11

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·August 5, 2024

    UNKNOWN ANKYLOS ABUTMENT

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·April 7, 2023

    ANK C/X IMPL A11/D3.5/L11

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·February 29, 2024

    UNKNOWN ANKYLOS ABUTMENT

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·September 7, 2022

    ANK IMPL A11 D3,5 MM/L11 MM

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·July 12, 2024

    ANK REG C/X GINGIVAF. GH 4,5

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·October 13, 2023

    SEGMENTED CYLINDER APPLICATOR SET

    FDA Adverse Event
    Other ·VARIAN MEDICAL SYSTEMS, INC.·Product code JAQ·June 5, 2013

    AQUALINE

    FDA Adverse Event
    Malfunction ·HAEMOTRONIC·Product code FJK·July 21, 2011

    WORKHORSE II BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·ANGIODYNAMICS, INC.·Product code LIT·September 11, 2008