49 results
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32ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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METASURG SUBTALAR IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
FREELITE KAPPA FREE KIT
FDA 510(k)
FDA Class 2
·Immunology
BODYGUARD
FDA 510(k)
FDA Class 2
·General Hospital
PRIMORIS HIP STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 5, 2016
PRIMORIS FEMORAL STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·October 3, 2017
PRIMORIS NECK PROSTH BM SZ 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 4, 2016
PRIMORIS HIP STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 5, 2016
PRMRS NCK STEM TI BM SZ 24 RSA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·June 23, 2016
TAPERLOC LAT COCR 10MM T1
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code JDI·March 20, 2026
TPRLOC COCR CMTD STEM T1 7.5MM
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code JDI·March 20, 2026
UNKNOWN PRIMORIS HIP
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 4, 2016
PRMRS NCK STEM TI BM SZ 24 RSA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWY·April 13, 2018
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·April 22, 2013
1.25MM THREADED GUIDE WIRE
FDA Adverse Event
Malfunction
·SYNTHES ELMIRA·Product code HWC·April 19, 2011
PROGRAMMING SOFTWARE
FDA Adverse Event
Malfunction
·CYBERONICS, INC.·Product code LYJ·July 3, 2008
CARTRIDGE
FDA Adverse Event
Injury
·GAMBRO RENAL PRODUCTS S.A. DE C.V.·Product code FJK·July 8, 2015
PRIMORIS NECK PROSTHESIS TI BM SIZE 26
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·November 9, 2017
UNKNOWN PRIMORIS HIP
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 4, 2016
UNKNOWN PRIMORIS HIP
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 5, 2016
PRMRS NCK STEM TI BM SZ 24 RSA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·April 13, 2018