FDA device listing

3.0T GEM Anterior Array (Aurora only),3.0T GEM HNU (Aurora only),3.0T GEM PA (Aurora only),3.0T GEM PVA (Aurora…

FDA device listing 1559491203 · GE HealthCare Technologies Inc.

Key facts

Proprietary names 3.0T GEM Anterior Array (Aurora only),3.0T GEM HNU (Aurora only),3.0T GEM PA (Aurora only),3.0T GEM PVA (Aurora only),Discovery MR750W,Discovery MR750w 3.0T,MR 750W
Owner/operator GE HealthCare Technologies Inc.
Owner/operator number 9912004
Premarket submissions K103327
Product codes LNH, LNI, MOS
Device names LNH - System, Nuclear Magnetic Resonance Imaging, LNI - System, Nuclear Magnetic Resonance Spectroscopic, MOS - Coil, Magnetic Resonance, Specialty
Device class Class II
Classification regulations (21 CFR) 892.1000
Review panels Radiology
Registered establishments GE Healthcare Coils, GE Healthcare Manufacturing LLC, GE HEALTHCARE (TIANJIN) COMPANY LIMITED, GE MEDICAL SYSTEMS, LLC, GE MEDICAL SYSTEMS MONTERREY MEXICO, S.A. DE C.V., WIPRO GE HEALTHCARE PRIVATE LTD
Establishment registrations 1529041, 2183553, 9613936, 9616047, 3005326970, 3010949642, 3015329423
FEI numbers 2183553, 1000571342, 3003377038, 3005214683, 3005326970, 3010949642, 3015329423
Establishment operations Manufacturer, Specification Developer
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 1–9 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

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