BEUDAMED
    83 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 ×

    Modified Alma Lasers Soprano XL™ Family ofMulti-Application & Multi-Technology Platforms [SopranoXL, SopranoXLi, SopranoICE and Soprano ICE Platinum] with Duo and Trio Diode Laser Modules., Soprano Duo and Trio Diode Laser Modules

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

    ARROW REVERSE SHOULDER SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COGENT MED-LIF XL

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code NKB·October 18, 2017

    ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC.·Product code NKB·February 13, 2020

    SLEEPSTYLE AUTO

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·January 2, 2025

    SLEEPSTYLE AUTO

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·February 18, 2025

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·April 11, 2022

    SLEEPSTYLE AUTO

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BZD·September 12, 2024

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT,

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK·Product code MAX·November 16, 2018

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·November 13, 2018

    CAPSTONE PTC SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·July 8, 2020

    ADVANCE 14 LP LOW PROFILE BALLOON CATHETER

    FDA Adverse Event
    Malfunction ·COOK INC·Product code LIT·September 12, 2019

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·December 7, 2017

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·April 1, 2020

    CRESCENT SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·October 11, 2021

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·March 22, 2019

    CRESCENT SPINAL SYSTEM

    FDA Adverse Event
    Malfunction ·MSD DEGGENDORF MFG·Product code MAX·January 7, 2019

    8800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 5, 2013

    LEAD MODEL UNKNOWN

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·September 11, 2008