40 results · 24ms · Sources: EU EUDAMED, US FDA

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AGNES

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

3M™ Unitek™

FDA UDI
3M UNITEK CORPORATION·00652221045485·Unitek(TM) Molar Band General Purpose Wide Regu...

OPTIBOND ALL-IN-ONE

FDA 510(k)
FDA Class 2 ·Dental

ARCOS INTERLOCKING DISTAL STEMS

FDA 510(k)
FDA Class 3 ·Orthopedic

BIODESIGN DURAL GRAFT

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

PENUMBRA MAX PUMP - INDIGO SYSTEM

FDA Adverse Event
Malfunction ·PENUMBRA INC., USA·Product code NRY·August 23, 2018

PENUMBRA SYSTEM 3MAX REPERFUSION CATHETER

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·March 8, 2018

SPRINT QUATTRO SECURE S

FDA Adverse Event
Injury ·MPRI·Product code LWS·June 10, 2013

ACCESS

FDA Adverse Event
Malfunction ·BIEFFE MEDITAL MANUFACTURING S.A.R.L. TUNIS·Product code FPA·July 13, 2011

TRIDENT HEMISPHERICAL CLUSTER HOLE SHELL

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·September 12, 2008

BIODESIGN DURAL GRAFT

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

PENUMBRA SYSTEM ASPIRATION PUMP MAX 220

FDA Adverse Event
Malfunction ·PENUMBRA, INC.·Product code NRY·April 9, 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