8 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BITE BLOCK #59430
FDA 510(k)
FDA Class 2
·Neurology
TRUSTEEL
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 18, 2024
TRUSTEEL
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·June 18, 2024
KeYi Spinal Fixation System
FDA 510(k)
FDA Class 2
·Orthopedic
ORTHODONTIC CERAMIC BRACKET
FDA 510(k)
FDA Class 2
·Dental
LUMOS DR-T
FDA Adverse Event
Malfunction
·BIOTRONIK SE & CO. KG·Product code LWS·October 29, 2010
RIATA ACTIVE FIXATION
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL INC., CRMD·Product code LWS·January 13, 2014
HEART START XL
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·November 15, 2012