58 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MODULAR VALVE HANDLES FOR ADAPTABLE TUBES, MODEL 1298-XX-XX, 1295-XX-XX
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040008010·Zirlux 16+ B3 89x17x12
Brite Shield
FDA UDI
PREMIER DENTAL PRODUCTS COMPANY·D6919011997·Brite Shield 10 Pack
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033355510·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033355534·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033355527·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033355503·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033355541·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033355497·
DESIGN OPTICS
FDA UDI
FGX INTERNATIONAL INC.·00193033355466·
ABBOTT AXSYM SYSTEM
FDA Adverse Event
Other
·ABBOTT MFG., INC.·Product code JJE·May 30, 1997
PAM-RL
FDA 510(k)
FDA Class 2
·Neurology
WHITE KNIGHT BLUE, GREEN FACE MASK, (4 MODELS)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
QUICK SET
FDA Adverse Event
Injury
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·November 18, 2025
HULKA FALLOPIAN TUBE CLIP
FDA Adverse Event
Malfunction
·RICHARD WOLF MEDICAL INSTRUME.·Product code HGB·July 31, 1998
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM FOR ADULTS
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·February 9, 1999
SOFTFORM FACIAL IMPLANT
FDA Adverse Event
Injury
·TISSUE TECHNOLOGIES, INC.·Product code FTL·January 8, 1999
UNK
FDA Adverse Event
Other
·SAFESKIN CORP.·Product code LYY·February 2, 1999
VENTAK P2 AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS·Product code LWS·May 8, 1997
VENTAK PRX2 AUTOMATIC IMPLANTABLE CARDIOVERTER DEFIBRILLATOR
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS·Product code LWS·May 8, 1997