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

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    Needle aspiration and injection

    FDA UDI
    KATENA PRODUCTS, INC.·00841668113608·PERIBULBAR NEEDLE 25GA 22MM

    EndoLIF Delta-Cage and DoubleWedge-Cage

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EVOS Lumbar Interbody System

    FDA UDI
    Cutting Edge Spine, LLC·00841193113579·HA PEEK EVOS Straight, ,14mmx9mmx 22mm , FLAT ...

    Responsive Respiratory

    FDA UDI
    RESPONSIVE RESPIRATORY, INC.·00851440007674·14' Supply Tubing, Green

    NA

    FDA UDI
    Stryker GmbH·07613154639915·Screw Marker 30,14

    VIANOX DELIVERY SYSTEM, MODEL I

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SOMATOM EMOTION MS

    FDA 510(k)
    FDA Class 2 ·Radiology

    SMS STEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·November 4, 2025

    SMS STEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·January 8, 2026

    SMS STEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·January 29, 2026

    BABYFLOW

    FDA Adverse Event
    Injury ·DRAEGER MEDICAL AG & CO. KG·Product code NHJ·October 21, 2008

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·August 11, 2011

    UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·July 2, 2013

    BALL HEADS: MECTACER 01.29.211 BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 36 SIZE XL

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·May 26, 2023

    MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142515, K153343, K173592, K202014, K231560.

    FDA Recall
    Open, Classified ·Siemens Medical Solutions USA, Inc·Product code LNH·August 28, 2025

    LINK SLED Knee System ENDO MODEL SLED TIBIAL COMP 8 MM X 50 MM Item Number: 15-2030/14

    FDA Recall
    Open, Classified ·Linkbio Corp.·Product code HSX·March 21, 2023

    SMS STEM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·November 18, 2025

    CUP: MPACT 01.32.148DH ACETABULAR SHELL Ø48 TWO-HOLES

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·October 28, 2022

    MECTACER BIOLOX DELTA FEMORAL BALL HEAD

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·February 12, 2025

    MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142515, K153343, K173592, K202014, K231560.

    FDA Enforcement
    Class I ·Ongoing·Siemens Medical Solutions USA, Inc·October 8, 2025