66 results · 24ms · 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.

PREXION3D ECLIPSE

FDA 510(k)
FDA Class 2 ·Radiology

ENDIUS ATAVI SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

OTOMAG BONE CONDUCTION HEARING SYSTEM MODEL ALPHA 1 (S) AND ALPHA 1 (M)

FDA 510(k)
FDA Class 2 ·Ear, Nose, Throat

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

CRESCENT SPINAL SYSTEM

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

INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT,

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

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·December 15, 2015

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

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

SELECT SECURE

FDA Adverse Event
Death ·MPRI·Product code NVY·May 21, 2013

SPECTRUM MONITOR

FDA Adverse Event
Malfunction ·MINDRAY DS USA, INC.·Product code MHX·September 18, 2014

NAVISTAR THERMOCOOL DIAGNOSTIC/ABLATION DEFLECTABLE TIP CATHETER

FDA Adverse Event
Malfunction ·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code OAD·June 13, 2011

CRESCENT SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MSD DEGGENDORF MFG·Product code MAX·July 10, 2020

CAPSTONE PTC SPINAL SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·April 14, 2020