34 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ASAHI ULTIMATEBROS 3 PTCA GUIDE WIRE
FDA 510(k)
FDA Class 2
·Cardiovascular
Endo Carry-On Procedure Kit
FDA UDI
MEDIVATORS INC.·00677964072857·The ENDO CARRY-ON Procedure Kit contains all of...
SURGITRON IEC II
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SAFE-STEER GUIDE WIRE SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
TAPERLC BMPC LAT 6.0X132 12/14
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code KWA·August 4, 2016
TAPERLOC PC 15.0 MM 12/14
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code KWA·August 4, 2016
LIGASURE ATLAS HANDSWITCHING 20CM
FDA Adverse Event
Malfunction
·COVIDIEN LLC (SHANGHAI)·Product code GEI·April 22, 2013
6600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 18, 2011
LEAD MODEL 302
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·August 6, 2008
TAPERLOC COMPLETE MICROPLASTY FEMORAL
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·January 20, 2017
LNCS DC-I
FDA Adverse Event
Malfunction
·MASIMO - 40 PARKER·Product code DQA·March 11, 2017
TPRLC 133 TYPE1 BM SO 11.0
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·September 12, 2018
TAPERLOC BONEMASTER POROUS AND HYDROXYAPETITE COATED STEM
FDA Adverse Event
Malfunction
·BIOMET UK LTD.·Product code KWA·May 26, 2017
TAPERLOC TYPE1 BM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·December 4, 2018
TPRLC 133 FP TYPE1 BM HO 10.0
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·November 13, 2018
TPRLC 133 MP TYPE1 BM HO 10.0
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code LPH·March 20, 2019
TAPERLOC STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·July 19, 2017
TAPERLOC FEMORAL STEM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code KWA·December 22, 2016
TAPERLOC COMPLETE PRIMARY FEMORAL POROUS-BONEMASTER REDUCED DISTAL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·August 6, 2018
TPRLC 133 FP TYPE1 BM SO 11.0
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWA·December 4, 2018