40 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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