34 results · 24ms · Sources: EU EUDAMED, 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