7 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Dillard Nasal Balloon Catheter
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
SMALL BONE LOCKING PLATING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
ENDOFORM DENTAL TEMPLATE
FDA 510(k)
FDA Unclassified
·Unknown
SUBDURAL ELECTRODES, DEPTH ELECTRODES, AND ANCHOR BOLTS
FDA Adverse Event
Injury
·AD-TECH MEDICAL INSTRUMENT CORP.·Product code GZL·June 14, 2019
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·June 17, 2013
TRIMA ACCEL PLT, PLS, RBC SET
FDA Adverse Event
Other
·CARIDIANBCT·Product code LKN·July 18, 2011
COAGUCHEK XS SYSTEM
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GJS·September 25, 2008