BEUDAMED
    40 results · 22ms · 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 ×

    HORIZONTAL-VERTICAL LUMBAR VALVE AND SPETZLER LUMBAR PERITONEAL SHUNT SYSTEMS

    FDA 510(k)
    FDA Class 2 ·Neurology

    Bur PM2-70 80K diamC Ø2.0 St

    FDA UDI
    Bien-Air Surgery SA·17630055519587·

    Preat

    FDA UDI
    Preat Corporation·00842092169933·Sagix 2.2 Model Analog (2-Pack)

    ILIZAROV

    FDA UDI
    Smith & Nephew, Inc.·03596010030641·3/4 RING 110MM FOR SMALL BONE FIXATOR

    Tasso+

    FDA UDI
    Tasso Inc.·00850038691004·

    Symmetry Olsen

    FDA UDI
    ASPEN SURGICAL PRODUCTS, INC.·00841785101151·

    CIDEX OPA SOLUTION

    FDA 510(k)
    FDA Class 2 ·General Hospital

    HUMMER IV MICRODEBRIDER SYSTEM

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

    AS VEGA PS TIBIAL PLATEAU CEMENTED T3

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code JWH·April 4, 2018

    UNK HUMERAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 19, 2026

    RSP SHOULDER

    FDA Adverse Event
    Injury ·ENCORE MEDICAL, L.P.·Product code KWS·September 24, 2015

    R SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code LIX·April 29, 2013

    VIPER2 FINAL TIGHTENER HANDLE

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES SPINE·Product code LXH·September 19, 2014

    UNKNOWN HUMERAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code MBF·March 26, 2026

    UNKNOWN HUMERAL STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code PHX·March 25, 2026

    COMPREHENSIVE SRS

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWT·March 25, 2026

    AS COLUMBUS REV F FEMUR CEMENTED F5L

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

    AS VEGA PS TIBIAL PLATEAU CEMENTED T3+

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

    AS VEGA PS TIBIAL PLATEAU CEMENTED T2

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018

    AS COLUMBUS REV F TIB.OFFSET CEMENT.T5

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code JWH·April 3, 2018