7 results
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21ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SHEATHES (NON-LATEX)
FDA 510(k)
FDA Class 2
·Radiology
VIVADENT FILPIN
FDA 510(k)
FDA Class 1
·Dental
BASAL DORSAL PLATES
FDA 510(k)
FDA Class 2
·Orthopedic
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·September 5, 2024
HIP STEM INSERTER
FDA Adverse Event
Malfunction
·ORTHO DEVELOPMENT CORP.·Product code LXH·December 22, 2010
RX VIATRAC 14 PLUS PERIPHERAL DILATATION CATHETER
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code LIT·February 15, 2013
FLANGE FIXTURE AND ABUTMENT
FDA Adverse Event
Injury
·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·July 29, 2014