7 results
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27ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MARK I TOTAL KNEE SYS. ARTHROPLASTY
FDA 510(k)
FDA Class 2
·Orthopedic
Masel
FDA UDI
Ortho Organizers, Inc.·00190707034801·.016 X .016 Upper Econo Nickel Titanium Archwires
XIVE TG ABUTMENTS
FDA 510(k)
FDA Class 2
·Dental
QXLINK
FDA 510(k)
FDA Class 2
·Radiology
FLORENCE BED
FDA Adverse Event
GROUPE BERTEC INC·Product code FNL·January 6, 2014
NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Injury
·COCHLEAR LTD.·Product code MCM·November 14, 2012
CAPSUREEPI
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVN·June 10, 2015