44 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OPTETRAK TOTAL KNEE SYSTEM, STRAIGHT STEM EXTENSIONS - ADDITIONAL SIZES
FDA 510(k)
FDA Class 2
·Orthopedic
Zirlux
FDA UDI
HENRY SCHEIN, INC.·H65890122510·Zirlux UCLA Plastic Abutment, Non-Engaging, com...
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00031568800962·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00031568800979·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00193033217917·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00031568800993·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00024021800999·
TO BE ASSIGNED
FDA UDI
FGX INTERNATIONAL INC.·00193033399859·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00031568800955·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00024021800968·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00024021800975·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00024021801538·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00024021800951·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00031568801488·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00024021801484·
E-Z READERS
FDA UDI
FGX INTERNATIONAL INC.·00031568801532·
HAEMOPHILUS/STREPTOCOCCUS PNEUMONIAE (HP) MIC PLATE
FDA 510(k)
FDA Class 2
·Microbiology
SPARC SLING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 12, 2013
KIT, SOLERA STANDARD DRIVER
FDA Adverse Event
Malfunction
·MEDTRONIC NAVIGATION , INC.·Product code HAW·February 2, 2011