8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KETAC-GLAZE
FDA 510(k)
FDA Class 2
·Dental
MINIMED QUICK-SET
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·June 11, 2024
MINIMED QUICK-SET
FDA Adverse Event
Injury
·UNOMEDICAL A/S·Product code FPA·June 11, 2024
TRANSVENOUS BALLOON TIPPED(FLOW DIRECTED) TEMP. PA
FDA 510(k)
FDA Class 3
·Cardiovascular
THE CALIFORNIA SPLINT
FDA 510(k)
FDA Class 2
·Cardiovascular
UNIFY CRT-D
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·June 19, 2014
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·December 25, 2012
ASR ACETABULAR CUPS 52
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·October 22, 2010