Endologix, Inc.

2 Musick, Irvine, United States, 92618

32 devices 33 registrations
✕ AU (TGA)
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Devices

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Showing 1–20 of 32 devices

Device Name US UK CA AU EU
ABDOMINAL STENT GRAFT SYSTEM - AUTOINJECTOR Not registered with US (FDA) Not registered with UK (MHRA) Registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
ABDOMINAL STENT GRAFT SYSTEM - FILL POLYMER KIT Not registered with US (FDA) Not registered with UK (MHRA) Registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
ABDOMINAL STENT GRAFT SYSTEM - OVATION PRIME Not registered with US (FDA) Not registered with UK (MHRA) Registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
AFX2 Bifurcated Endograft System Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
AFX2 Endovascular AAA System Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
AFX Introducer Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Registered with EU (EUDAMED)
AFX INTRODUCER SYSTEM Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
AFX Stand Alone Endograft System Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
AFX Vela Endograft System Not registered with US (FDA) Registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
Alto Abdominal Stent Graft System Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
ALTO AB STENT GRAFT SYSTEM Not registered with US (FDA) Not registered with UK (MHRA) Registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
Alto™ Aortic Body Stent Graft Not registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Registered with EU (EUDAMED)
Auto Injector 2 Not registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Registered with EU (EUDAMED)
AUTOINJECTOR 2 Not registered with US (FDA) Not registered with UK (MHRA) Registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
CUSTOMSEAL KIT Not registered with US (FDA) Not registered with UK (MHRA) Registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
CustomSeal™ Polymer Fill Kit Not registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Registered with EU (EUDAMED)
DETOUR System Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
DUAL LUMEN CATHETER Not registered with US (FDA) Not registered with UK (MHRA) Registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
DUAL LUMEN CATHETER, MODEL DL-35-90 Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
ENDOLOGIX AFX INTRODUCER SYSTEM Registered with US (FDA) Not registered with UK (MHRA) Not registered with Canada (Health Canada) Not registered with AU (TGA) Not registered with EU (EUDAMED)
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