32 results
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24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Reveal LINQ
FDA 510(k)
FDA Class 2
·Cardiovascular
BONASTENT® Tracheal/Bronchial
FDA UDI
Sewoon Medical Co., Ltd.·08806369468947·
B-P TOTAL HIP SYSTEM
FDA UDI
ENDOTEC, INC.·00814193024640·B-P MODULAR EXTENSION W/ULTRACOAT - 9 MM X 200 MM
OSTEO-LINK BONE VOID FILLER PELLETS
FDA 510(k)
FDA Class 2
·Orthopedic
WIRELESS MONITORING SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
BIODESIGN DURAL GRAFT
FDA Adverse Event
Injury
·COOK BIOTECH·Product code GXQ·December 4, 2017
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 23, 2025
PRODIGY AUTOCODE
FDA Adverse Event
Injury
·OK BIOTECH CO., LTD.·Product code NBW·May 31, 2017
CAPSUREFIX
FDA Adverse Event
Injury
·MPRI·Product code NVN·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
UNKNOWN ZIMMER HIP
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JDI·July 7, 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