10,000 results
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31ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Waterpik PowerPulse with Qwik-Pause
FDA UDI
WATER PIK, INC.·00073950299695·Hand held shower head, brushed nickel
Waterpik PowerPulse with Qwik-Pause
FDA UDI
WATER PIK, INC.·00073950300506·Hand held shower head, black
Waterpik PowerPulse with Qwik-Pause
FDA UDI
WATER PIK, INC.·00073950293440·Hand held shower head, brushed nickel
Sinon Ruby Laser System (silver)
FDA UDI
ALMA LASERS LTD.·17290110121485·
IDAS Laser system 532 nm
FDA UDI
ALMA LASERS LTD.·17290110121171·
Sinon Ruby Laser System (Dummy)
FDA UDI
ALMA LASERS LTD.·17290110121195·
308 Excimer System
FDA UDI
ALMA LASERS LTD.·17290110121133·
ARION Alexandrite Laser System
FDA UDI
ALMA LASERS LTD.·17290110121157·
Sinon Ruby Laser System
FDA UDI
ALMA LASERS LTD.·17290110121140·
BURANE II System
FDA UDI
ALMA LASERS LTD.·17290110121126·
EXELO2 CO2 Laser System
FDA UDI
ALMA LASERS LTD.·17290110121164·
MYDON Nd:YAG Laser System
FDA UDI
ALMA LASERS LTD.·17290110121188·
SYNCHROMED II
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code LKK·November 21, 2016
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Malfunction
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·May 21, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·April 9, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·April 9, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·April 17, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·April 17, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·May 8, 2026
GORE® VIABAHN® FORTEGRA VENOUS STENT
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code QTL·March 9, 2026