49 results · 32ms · Sources: EU EUDAMED, 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