26 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODIFICATION TO ALLOY PRIMER
FDA 510(k)
FDA Class 2
·Dental
Zirlux
FDA UDI
HENRY SCHEIN, INC.·00304040070642·Zirlux Acetal P1 98x15
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151231·NC TREK Coronary Dilatation Catheter 2.75 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151194·NC TREK Coronary Dilatation Catheter 2.75 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151200·NC TREK Coronary Dilatation Catheter 2.75 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151217·NC TREK Coronary Dilatation Catheter 2.75 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151224·NC TREK Coronary Dilatation Catheter 2.75 mm x ...
QUICK SET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·January 9, 2026
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408926·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408902·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408919·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408940·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408957·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033408933·
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 12, 2025
MOBILE-PATIENT VIEWER
FDA 510(k)
FDA Class 2
·Cardiovascular
TEMPUS 2000 PATIENT MONITOR, MODEL 00-0001; TEMPUS MONITORING STATION, MODEL 01-0011
FDA 510(k)
FDA Class 2
·Cardiovascular
QUICK SET
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·November 10, 2025
MAGELLAN
FDA Adverse Event
Malfunction
·CARDINAL HEALTH, INC.·Product code FMI·September 6, 2023
CHARGING SYSTEM
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·March 15, 2013