12 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TrueFit Bolus; TrueFlex Bolus
FDA 510(k)
FDA Class 2
·Radiology
Oph. Cystotomes
FDA UDI
KATENA PRODUCTS, INC.·00841668113677·CYSTOTOME STRAIGHT 27GA
3D Printed Interbody Systems
FDA UDI
Seaspine Orthopedics Corporation·10889981281434·Interbody, 14x13x5mm, 7 Degree, 3D
WaveForm™ C
FDA UDI
Seaspine Orthopedics Corporation·10889981219994·Interbody, 14x13x5mm, 7 Degree, 3D
Accogent Pausch
FDA registration
Accogent Pausch·13 products·🇺🇸 United States
M3290B Philips IntelliVue Information Center iX
FDA 510(k)
FDA Class 2
·Cardiovascular
Quantum Perfusion Arterial Cannula Graft
FDA 510(k)
FDA Class 2
·Cardiovascular
OPTI-FREE REPLENISH
FDA Adverse Event
Injury
·ALCON - FORT WORTH ASPEC /ALCON LABORATORIES, INC.·Product code LPN·November 21, 2008
CURRENT ACCEL VR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 11, 2011
ULTRACISION HARMONIC ACE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code LFL·July 23, 2013
PATIENT INFORMATION CENTER IX
FDA Adverse Event
Injury
·PHILIPS MEDICAL SYSTEMS·Product code MHX·December 4, 2023
Fortify, Sterile EO, Model #/ Part #: CD1231-40/100029238,100030095, 100041981; CD1231-40Q/100029229, 100030087, 100041982; CD1233-40/100029230, 100029250, 100029259,100031058, 100059778, 100070017; CD1233-40Q/100029260, 100029271, 100029277, 100031104, 100070089; CD1235-40/100029272, 100029282, 100029311, 100031039, 100059779; CD1235-40Q/100029273, 100029295, 100029312, 100030840; CD1241-40/100046351; CD1241-40Q/100046167; CD2231-40/100029274, 100030110, 100041922; CD2231-40Q/100029275, 100030089, 100041923; CD2233-40/100029147, 100029276, 100029313, 100031066, 100037043, 100048759, 100070007; CD2233-40Q/100029148, 100029263, 100029314, 100031067, 100037044, 100059770, 100070068; CD2235-40/100029149, 100029265, 100029283, 100031029, 100059837; CD2235-40Q/100029239, 100029258, 100029284, 100031030, 100066504; CD2241-40/100046148; CD2241-40Q/100046149; CD2299-40/100056952
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018