BEUDAMED
    34 results · 23ms · 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 ×

    ZS3 and z.one pro Ultrasound Systems

    FDA 510(k)
    FDA Class 2 ·Radiology

    Echo® Bi-Metric® Hip System

    FDA UDI
    Biomet Orthopedics, LLC·00887868260711·

    ECHO BI-METRIC HIP SYSTEM

    FDA UDI
    Biomet Orthopedics, LLC·00880304463004·

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694009676·2.4mm x 10mm Cannulated Lag Screw

    Orthos

    FDA UDI
    ORMCO CORPORATION·00889989030334·ORTHOS CM TMA 017 X 025 UPLG PK10

    Symetri Clear

    FDA UDI
    ORMCO CORPORATION·00889989083071·L3R SYMETRI CLEAR MCLAUGHLIN, BENNETT & TREVISI...

    APEX Knee System

    FDA UDI
    Omni Life Science, Inc.·00841690198659·AK3 Ultra Insert Trial Size 4, 10mm

    OsteoMed

    FDA UDI
    OSTEOMED LLC·00845694070584·Cannulated 2.4 x 10mm Lag Screw Sterile Qty 5

    I RUNE (I-200L)

    FDA 510(k)
    FDA Class 2 ·Neurology

    MATRYX INTERFERENCE SCREW (5.0-6.5MM)

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    EXPERIENCE®

    FDA UDI
    Gc Orthodontics America Inc.·D78819241000101·EXMRC ROTH 022/LR 1 & 2 - 1T 2A

    Responsive Orthopedics Total Knee Arthroplasty System

    FDA UDI
    RESPONSIVE ORTHOPEDICS, LLC·00841973108092·TRIAL 90-SRK-192410 POLY-MPCS 4X10 LEFT

    CERTAIN® GOLD-TITE® HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·June 19, 2019

    CERTAIN® GOLD-TITE® HEXED SCREW

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code NHA·June 19, 2019

    ACTIVE ARTICULATION E1 HIP BEARING

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LPH·August 24, 2016

    M2A MAGNUM PF CUP 54MM O.D. X 48MM I.D.

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWA·August 24, 2016

    BIOLOX DELTA MODULAR CERAMIC HEAD 28MM HEAD DIAMETER TYPE 16/18 TAPER

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code LZO·August 24, 2016

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·October 22, 2014

    CORE BIOPSY NEEDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY·Product code KNW·August 1, 2011

    2.7MM TI VA LCKNG SCR SLF-TPNGWITH T8 STARDRIVE RECESS 26MM

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·June 27, 2013