9 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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XIPHOS
FDA 510(k)
FDA Class 2
·Orthopedic
REACTIVE SKIN DECONTAMINATION LOTION
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
AC LENS BRANDED CONTACT LENS CASE
FDA 510(k)
FDA Class 2
·Ophthalmic
U-BLADE SET, TI GAMMA3 10.5X90MM
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·November 30, 2012
DERMABOND ADVANCED
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code MPN·May 22, 2013
U-BLADE SET, TI GAMMA3 Ø10.5X80MM
FDA Adverse Event
Injury
·STRYKER TRAUMA KIEL·Product code HSB·September 27, 2014
DA+ C SERIES DR
FDA Adverse Event
Injury
·MEDTRONIC S.A.·Product code DXY·June 14, 2011
TALENT AAA STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·May 8, 2025
ENDURANT STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·May 8, 2025