7 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EPI-LOCK WOUND DRESSING
FDA 510(k)
FDA Unclassified
·Unknown
Arthrex®
FDA UDI
ARTHREX, INC.·00888867138384·HOHMANN RETRTR 9 1/2" LNG,17MM PNTD
DURACON MODULAR FEMORAL COMPONENT AND FEMORAL SPAC
FDA 510(k)
FDA Class 2
·Orthopedic
SPLITTABLE SHEATH INTRODUCER SET
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MANDIBMESH FOOTPL2 TYPE C F/CMF DISTRACT
FDA Adverse Event
Injury
·SYNTHES BRANDYWINE·Product code MQN·January 23, 2013
1X8 TEST STIMULATION LEAD
FDA Adverse Event
Malfunction
·MPROC, VILLALBA·Product code GZB·November 10, 2010
TENDRIL STS
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 10, 2014