25 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
VHS PEDIATRIC HIP SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040009420·Zirlux 16+ A3.5 coloring liq
NA
FDA UDI
Stryker GmbH·00886385006468·Carpal Fusion Plate Screw
MASEL
FDA UDI
Ortho Organizers, Inc.·00190707053871·GeoShapes™ Elastics 1/4" (6.35 mm) Extra Heavy ...
GeoShapes™ Elastics
FDA UDI
Ortho Organizers, Inc.·00190707097394·GeoShapes™ Elastics 1/4" (6.35 mm) Extra Heavy ...
READERS CHOICE
FDA UDI
FGX INTERNATIONAL INC.·00193033300916·
READERS CHOICE
FDA UDI
FGX INTERNATIONAL INC.·00193033300978·
READERS CHOICE
FDA UDI
FGX INTERNATIONAL INC.·00193033301036·
READERS CHOICE
FDA UDI
FGX INTERNATIONAL INC.·00193033300947·
READERS CHOICE
FDA UDI
FGX INTERNATIONAL INC.·00193033301043·
READERS CHOICE
FDA UDI
FGX INTERNATIONAL INC.·00193033301012·
READERS CHOICE
FDA UDI
FGX INTERNATIONAL INC.·00193033300787·
TRUSTEEL
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 31, 2025
SAFESTING AND SAFESTING HUB
FDA 510(k)
FDA Class 2
·General Hospital
REPROBEAD T4 ENZYME IMMUNOASSAY REAGENT KIT (CATALOG# 105)
FDA 510(k)
FDA Class 2
·Clinical Chemistry
HEARTMATE 3 LVAS IMPLANT KIT
FDA Adverse Event
Death
·THORATEC CORPORATION·Product code DSQ·January 26, 2023
TRUSTEEL
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 4, 2025
CONTACT DETACH
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·September 11, 2025
XIENCE PRIME SV EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code NIQ·March 19, 2013
CONTINU-FLO SOLN. SET, 3 LUERACTIVATED VALVES
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE·Product code FPA·March 9, 2011