9 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
mollosil plus
FDA 510(k)
FDA Class 2
·Dental
BD ULTRA FINE¿ PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON AND CO.·Product code FMI·February 18, 2020
DEPUY SIGMA CRUCIATE RETAINING POROCOAT FEMORAL COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
VERTEX RAPID SIMPLIFIED
FDA 510(k)
FDA Class 2
·Dental
BD ULTRA FINE¿ PEN NEEDLES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND CO.·Product code FMI·January 14, 2020
PENUMA IMPLANT
FDA Adverse Event
Injury
·INTERNATIONAL MEDICAL DEVICES, INC.·Product code MIB·October 7, 2019
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA, INC.·Product code KRG·October 10, 2014
GYNECARE TVT OBURATOR SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·June 11, 2013
INSIGNIA
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 14, 2011