BEUDAMED
    76 results · 26ms · 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 ×

    ALOE CADABRA LUBRICANT, ALOE CADABRA FLAVORED/SCENTED LUBRICANTS

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    CANCELLOUS LOCKING SCREW, FULLY THREADED 4.0mm x 44mm

    FDA UDI
    ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665033656·

    Logical C-Series

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215004903·

    ARTHREX UNIVERSII XL GLENOID-PEGGED, ARTHREX UNIVERS II XL GLENOID-KEELED

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SABER TECH IMPLANTS SYSTEM

    FDA 510(k)
    FDA Class 2 ·Dental

    MECTALIF ANTERIOR STAND-ALONE PLATE FLUSH H.12 MM

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code OVD·March 29, 2018

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 17, 2013

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·June 14, 2011

    VERSACARE

    FDA Adverse Event
    Malfunction ·HILL-ROM RITTER·Product code FNL·August 20, 2008

    DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code QBJ·May 20, 2025

    CN LOCK SCREW, F THREAD, Ø4.0MM X 44MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·March 6, 2025

    CN LOCK SCREW, F THREAD, Ø4.0MM X 42MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·March 6, 2025

    LO-PRO SCRW,TI,3.5MMX 24MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·March 6, 2025

    CORTICAL BONE SCREW, Ø3.5MM X 28MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·March 6, 2025

    CN LOCK SCREW, F THREAD, Ø4.0MM X 44MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·March 6, 2025

    CN LOCK SCREW, F THREAD, Ø4.0MM X 36MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·March 6, 2025

    CORTICAL BONE SCREW, Ø3.5MM X 26MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·March 6, 2025

    CN LOCK SCREW, F THREAD, Ø4.0MM X 38MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·March 6, 2025

    CN LOCK SCREW, F THREAD, Ø4.0MM X 36MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·March 6, 2025

    CT SCREW DOUBLE LEAD LOCK, Ø3.5MM X 26MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KTW·March 6, 2025