61 results
·
38ms
·
Sources: EU EUDAMED, US FDA
IND ONE STEP HCG PREGNANCY TEST - CASSETTE FORMAT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
EMS JUMPER II DUAL CHANNEL NEUROMUSCULAR STIMULATOR SYSTEM, MODEL E-188
FDA 510(k)
FDA Class 2
·Physical Medicine
UNICONDYLAR KNEE
FDA 510(k)
FDA Class 2
·Orthopedic
PRIMORIS HIP STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 5, 2016
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026
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
COBAS E411 DISK SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code MMI·April 10, 2013
CONTAK RENEWAL
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·April 12, 2011
CURRENT RF DR
FDA Adverse Event
Malfunction
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·May 27, 2008
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