8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OSTEONICS CDH HIP STEM
FDA 510(k)
FDA Class 2
·Orthopedic
UCR
FDA UDI
Seaspine Orthopedics Corporation·10889981080259·COMBINATION WRENCH 3/16"
PATIENT MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
TRI-FIX SPINAL FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
INCEPTA
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013
DAVINCI HARMONIC CURVED SHEARS INSERT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL·Product code NAY·November 15, 2010
ELLIPSE DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code LWS·July 2, 2014
Pipeline Flex Embolization Device
FDA Enforcement
Class I
·Ongoing·Micro Therapeutics Inc,·September 15, 2021