213 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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BIOGEL LATEX POWDER FREE STERILE SURGEON'S GLOVE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Premier H-FILES
FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·D6919053441·FILES HDSTROM PKG 6 25MM 15-40
CASTLE MODEL 233HC STEAM STERILIZER
FDA 510(k)
FDA Class 2
·General Hospital
ISOLA POLYAXIAL WASHER
FDA 510(k)
FDA Class 2
·Orthopedic
PRIMORIS HIP STEM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·August 5, 2016
ARCHITECT C4000 ANALYZER
FDA Adverse Event
Injury
·ABBOTT MANUFACTURING INC·Product code MZV·April 11, 2013
TURON SHOULDER INSTRUMENT
FDA Adverse Event
Malfunction
·ENCORE MEDICAL, L.P.·Product code KWS·March 1, 2011
HYLAMER 10D 54OD X 28ID
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWY·May 27, 2008
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
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026
PRMRS NCK STEM TI BM SZ 24 RSA
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code JDI·June 23, 2016
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
TAPERLOC LAT COCR 10MM T1
FDA Adverse Event
Death
·BIOMET UK LTD.·Product code JDI·March 20, 2026