BEUDAMED
    13 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 ×

    Milagro / Milagro Advance Interference Screw

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COLD PACK, PLASTIC APPLICATOR (MEDICAL GRADE)-NON-CHEMICAL

    FDA 510(k)
    FDA Unclassified ·Unknown

    LANX CERVICAL INTERVERTEBRAL BODY FUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Added Screen Displays For FDA Cleared HeartSee Cardiac P.E.T Processing Software K143664

    FDA 510(k)
    FDA Class 2 ·Radiology

    WEP-4208A

    FDA Adverse Event
    Malfunction ·NIHON KOHDEN CORPORATION·Product code MHX·August 12, 2014

    GEL OVATIONS 314 G

    FDA Adverse Event
    Injury ·Product code KNN·December 27, 2007

    PULSE GEN MODEL UNK

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·August 28, 2008

    INTIMA II¿ CLOSED IV CATHETER SYSTEM

    FDA Adverse Event
    Malfunction ·BD (SUZHOU)·Product code FOZ·October 31, 2018

    TRULIANT TIB IMP PS INSERT SZ 3 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 31, 2023

    2.4MM STERNALOCK (TM) SYSTEM SELF-DRILLING SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·January 10, 2020

    STERNALOCK BLU SYSTEM PLATE, 8 HOLE STRAIGHT

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·January 10, 2020

    STERNALOCK BLU SYSTEM PLATE, 8 HOLE STRAIGHT

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·January 10, 2020

    2.4MM STERNALOCK (TM) SYSTEM SELF-DRILLING SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code HRS·January 10, 2020