180 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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EX-PRESS MINATURE GLAUCOMA IMPLANT, MODELS R-20, R-30, R-50, STS VERSIONS
FDA 510(k)
FDA Class 2
·Ophthalmic
GC Initial™
FDA UDI
Gc America Inc.·D0470128521·Initial LiSi Press Ingot LT-D3 (3gx5)
AcQGuide Mini-S
FDA UDI
ACUTUS MEDICAL, INC.·00857042007500·AcQGuide Mini-S, 65cm - L2 with AcQCross QX
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756284271·LAPAROTOMY TRAY
Mini Sheath with FlexCath Cross
FDA UDI
ACUTUS MEDICAL, INC.·00850027837697·Mini sheath, 65cm – L2 with FlexCath Cross
EYE SENTIAL
FDA UDI
FGX INTERNATIONAL INC.·00193033444542·
OSMED TISSUE EXPANDER
FDA 510(k)
FDA Class 2
·Ophthalmic
N/T PROTEIN CONTROL SL
FDA 510(k)
FDA Class 1
·Clinical Chemistry
PRECISION®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·March 20, 2013
GORE EXCLUDER AAA ENDOPROSTHESIS
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MIH·March 1, 2011
LIFEPAK 500 AUTOMATED EXTERNAL DEFIBRILLATOR
FDA Adverse Event
Malfunction
·PHYSIO-CONTROL, INC.·Product code MKJ·March 12, 2008
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026