41 results · 22ms · Sources: EU EUDAMED, US FDA

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FDA 510(k)
FDA Class 2 ·General Hospital

CoRoent

FDA UDI
Nuvasive, Inc.·00887517291974·CoRoent® XLFW, 8x22x60mm

CoRoent

FDA UDI
Nuvasive, Inc.·00887517730824·CoRoent XL+, 8x18x60mm 15°

Malibu™

FDA UDI
Seaspine Orthopedics Corporation·10889981029463·ILIAC MONOAXIAL, 8.5 x 60mm

TURKOM-CERA

FDA 510(k)
FDA Class 2 ·Dental

COMP A-I-R

FDA 510(k)
FDA Class 2 ·Anesthesiology

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

CARELINK

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

OT VERIO IQ METER

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

MEDISENSE OPTIUM

FDA Adverse Event
Malfunction ·Product code NBW·July 13, 2011

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·May 7, 2018

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017