7 results
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35ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DERMICEL, MONTGOMERY STRAP
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
Telepack X LED
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
DENTAL MOUTH PROP.
FDA 510(k)
FDA Class 2
·Neurology
LIGHT MONITOR
FDA Adverse Event
Malfunction
·GE HEALTHCARE FINLAND, OY·Product code DRT·October 13, 2010
VITROS IMMUNODIAGNOSTIC PRODUCTS TROPONIN I ES REAGENT
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS·Product code MMI·December 20, 2012
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·June 19, 2014
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·November 21, 2023