27 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MODIFICATION TO PANAVIA 21
FDA 510(k)
FDA Class 2
·Dental
Zirlux
FDA UDI
HENRY SCHEIN, INC.·00304040070666·Zirlux Acetal P1 98x25
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151309·NC TREK Coronary Dilatation Catheter 3.25 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151347·NC TREK Coronary Dilatation Catheter 3.25 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151330·NC TREK Coronary Dilatation Catheter 3.25 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151316·NC TREK Coronary Dilatation Catheter 3.25 mm x ...
NC TREK
FDA UDI
ABBOTT VASCULAR INC.·08717648151323·NC TREK Coronary Dilatation Catheter 3.25 mm x ...
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409077·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409046·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409039·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409022·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409053·
DISNEY
FDA UDI
FGX INTERNATIONAL INC.·00193033409060·
CURLIN ADMINISTRATIN SET
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICES GROUP·Product code FRN·August 24, 2011
MAXITEX DUPLEX POWDER FREE LATEX STERILE SURGEON GLOVES PROTEIN LABELING CLAIM (50 MICRGRAMS OR LESS)
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
BILATERAL FITTING OF THE BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM.
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
Phonak
FDA UDI
Phonak AG·07613275081549·Phonak Bolero Q50-M13 (purple transparent)
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 5, 2025
INSET
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 5, 2025
CURLIN ADMINISTRATION SET
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICES GROUP·Product code FRN·January 31, 2011