9 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NIRVANA
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SIENTRA SILICONE GEL BREAST IMPLANTS
FDA Adverse Event
Injury
·SIENTRA INC·Product code FTR·September 12, 2024
LACRYTEST
FDA 510(k)
FDA Class 2
·Immunology
STATIM 6000B Vacuum Autoclave
FDA 510(k)
FDA Class 2
·General Hospital
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·August 22, 2025
BD MICROLANCE¿ HYPODERMIC NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMI·February 22, 2018
TAXUS LIBERTE' PACLITAXEL-ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code NIQ·November 4, 2008
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code MDS·August 29, 2011
GYNECARE TVT OBURATOR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·July 18, 2013