7 results
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34ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Chameleon PTA Balloon Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
MICROBLADE SHAVER AND ACCESSORIES
FDA 510(k)
FDA Class 2
·Neurology
KYPHON INFLATION SYRINGE
FDA 510(k)
FDA Class 2
·Orthopedic
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 28, 2014
GYNECARE PROLIFT TOTAL PELVIC FLOOR REPAIR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTP·June 11, 2013
UNKNOWN DEPUY PATELLA
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code HTG·July 8, 2011
ADVIA CENTAUR TROPONIN ULTRA ASSAY
FDA Adverse Event
Other
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code MMI·September 15, 2008