BEUDAMED
    1,397 results · 39ms · 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 ×

    Holmium Laser Therapeutic Apparatus

    FDA UDI
    Guangzhou Potent Medical Equipment Joint-Stock Co., Ltd.·06973204212224·

    CYAN ADP HIGH SPEED ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC.·Product code GKZ·August 31, 2010

    ASTRATECH IMPL EV 4.2S 11MM OS

    FDA Adverse Event
    Injury ·DENTSPLY IMPLANTS MANUFACTURING GMBH·Product code DZE·March 18, 2026

    KINETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC EUROPE SARL·Product code MHY·November 16, 2010

    EXTERNAL NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·September 20, 2016

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·November 3, 2020

    LEAD MODEL UNKNOWN

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·February 19, 2013

    Holmium Laser Therapeutic Apparatus (HZ-A); Holmium Laser Therapeutic Apparatus (HZ-B); Holmium Laser Therapeutic Apparatus (HZ-E)

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    INTERSTIM

    FDA Adverse Event
    Injury ·IPG MFG SWITZERLAND·Product code EZW·March 9, 2012

    KINETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·May 21, 2015

    ACTIVA RC

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code MHY·June 8, 2011

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MFR·July 1, 2015

    OUS UPS 2ND GEN

    FDA Adverse Event
    Malfunction ·BLUE BELT TECHNOLOGIES·Product code OLO·April 23, 2020

    ACTIVA

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MFR·July 1, 2015

    TEO

    FDA Adverse Event
    Malfunction ·MICROPORT CRM S.R.L.·Product code LWP·November 12, 2024

    INTELLIS

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LGW·January 23, 2019

    Methyl Green

    FDA classification
    FDA Class 1 ·Methyl Green

    OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119.

    FDA Enforcement
    Class II ·Ongoing·Olympus Corporation of the Americas·April 29, 2026

    HDA TECHNOLOGY, INC.

    FDA registration
    HDA TECHNOLOGY, INC.·2 products·🇺🇸 United States

    FUSION

    FDA UDI
    DANVILLE MATERIALS, LLC·00816594023727·FUSION,VPS,ZERO-ALGIN,50ML