24 results · 25ms · 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.

Nanovis Intervertebral Body Fusion System and FortiCore®

FDA 510(k)
FDA Class 2 ·Orthopedic

LIPOSONIX SYSTEM, MODEL 1 P00XXXX

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

DEPUY GLOBAL AP SHOULDER SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

INFINION 16

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·January 24, 2020

CARELINK

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code KRG·October 10, 2014

OT VERIO PRO METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

ALLEGRETTO WAVE EYE-Q

FDA Adverse Event
Malfunction ·WAVELIGHT GMBH·Product code LZS·June 16, 2011

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·April 18, 2019

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·March 2, 2020

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·March 18, 2021

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·April 21, 2021

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·June 21, 2019

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·January 25, 2024

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·January 29, 2019

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·March 12, 2020

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·March 12, 2020

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·December 8, 2022

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·March 31, 2022

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·October 10, 2019

Artis zeego, Material no. 10280959 , for angiography and whole body radiographic/fluoroscopic procedures.

FDA Enforcement
Class II ·Terminated·Siemens Medical Solutions USA, Inc·July 4, 2018