12 results · 19ms · Sources: EU EUDAMED, 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