8 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DEPUY MOTECH MOSS MIAMI SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EDENTA
FDA UDI
EDENTA ETABLISSEMENT·E312K90044710001·Dowel Pin 17 mm
reVive Light Therapy LED Cleansing System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SURGICRAFT SCREW FIXATION SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SUPRACONDYLAR NAIL T2 SCN 10 X 200 MM
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS ¿ KIEL·Product code HSB·July 17, 2012
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON INC·Product code OTN·February 27, 2013
STARCLOSE SE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·February 7, 2011
ACCU-CHEK ® AVIVA COMBO
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code NBW·August 5, 2014