Omni

Omni Gantry 24-30 Incl. Electronics Assy

Registry build 21.09.26
4manufacturers in China registered for this device type
1catalogue number

Who Else Makes It

Concentrated in Beijing (1), Shanghai (1), Guangdong (1).

Chinese manufacturers registered for FDA product code KPS
Manufacturer City Province Registered as Device types
GE Hangwei Medical Systems Co., Ltd. Beijing Beijing Specification developer 22
Shanghai United Imaging Healthcare Co., Ltd. Shanghai Shanghai Manufacturer 12
Siemens Shenzhen Magnetic Resonance Ltd. Shenzhen Guangdong Contract manufacturer 8
Neusoft Positron Medical Systems Co., Ltd. Shen Yang Liaoning Manufacturer 1

Record

Regulatory record for Omni
Listed by G E Medical Systems Israel Ltd.
FDA product code KPS
Device type System, Tomography, Computed, Emission
Device class Class 2
Regulation 21 CFR 892.1200
510(k) K221932
Record published 2022-09-12
Record revised 2026-01-30 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number, serial number

Catalogue Numbers

Catalogue numbers for Omni
Catalogue number Size Status
Legend In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
NeuroQ Syntermed, Inc. 11
Emory Cardiac Toolbox Syntermed, Inc. 10
Discovery GE Medical Systems, L.L.C. 7
uMI Shanghai United Imaging Healthcare Co., Ltd. 7
Brightonix Brightonix Imaging Inc. 6
UltraSPECT Ultraspect USA, LLC 5
Discovery G E Medical Systems Israel Ltd. 5
Veriton CT Spectrum Dynamics Medical Ltd. 5
Cardius 2 Digirad Corp. 4
Encompass™ SRS Fibreplast™ System Qfix 4
Veriton NM Spectrum Dynamics Medical Ltd. 3
Cedars-Sinai Cardiac Suite Cedars Sinai Medical Center 3

Showing 12 of 172. All products under System, Tomography, Computed, Emission

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Omni
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
GE Medical Systems Israel, Functional Imaging 510(k) number 2025-12-24 Class II Software design There is a potential intermittent issue on certain Omni Legend systems that can result in a streaking artifact in the PET clinical scan images. This streaking artifact is most easily identified in transaxial slices on the acquisition conso 364 units

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer