Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3014209556

FEI Number

3014209556

Entity Name

LIVERMORETECH,INC

City/State/Country

Plano, TX, US

Establishment Address

801 north Jupiter rd suite 200, Plano, TX 75074, US

Establishment Type(s)

Remanufacture Medical Device,Repack or Relabel Medical Device

Owner / Operator

LIVERMORETECH,INC (Owner Number: 10056565)

Owner / Operator Contact Address

801 Jupiter Rd, Suite 200, Plano, TX 75074, US

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

LMT1417W AIRTOUCH, PORTABLE X-RAY SYSTEM; EZER, PORTABLE X-RAY SYSTEM LMT1717W SYSTEM, X-RAY, STATIONARY, SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER) TE-90; TE-90(P) AIRTOUCH, PORTABLE X-RAY SYSTEM; EUROPA, PORTABLE X-RAY SYSTEM; EZER, PORTABLE X-RAY SYSTEM LMT1717W TE-90; TE-90(P)

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
MQB	Solid State X-Ray Imager (Flat Panel/Digital Imager)	Radiology	Class 2	892.1680	2021-01-18
EHD	Unit, X-Ray, Extraoral With Timer	Dental	Class 2	872.1800	2019-12-23
MQB	Solid State X-Ray Imager (Flat Panel/Digital Imager)	Radiology	Class 2	892.1680	2021-01-18
MQB	Solid State X-Ray Imager (Flat Panel/Digital Imager)	Radiology	Class 2	892.1680	2023-02-23
KPR	System, X-Ray, Stationary	Radiology	Class 2	892.1680	2023-02-23
KXJ	Table, Radiologic	Radiology	Class 2	892.1980	2020-06-08
IZL	System, X-Ray, Mobile	Radiology	Class 2	892.1720	2020-05-08
MQB	Solid State X-Ray Imager (Flat Panel/Digital Imager)	Radiology	Class 2	892.1680	2021-04-14
KXJ	Table, Radiologic	Radiology	Class 2	892.1980	2020-06-08

Official Correspondent

No official correspondent registered.

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LIVERMORETECH,INC

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K070563	Vidar Systems Corp.	VIDAR VISION 2000	2007-03-16
K190691	Pixxgen Corporation	Pixx2430 Digital Diagnostic X-Ray Receptor Panel	2019-04-04
K150150	Rayence Co., Ltd.	1717SGN / 1717SCN Digital Flat Panel X-ray Detector	2015-03-27
K140771	Philips Medical Systems Dmc GmbH	PHILIPS ELEVA WORKSPOT	2014-04-25
K991310	Villa Sistemi Medicali S.P.A.	EXPLOR-X 70	1999-06-18

Related Recall Records

Recall ID	Recalling Firm	Recall Class	Product Description
Z-0005-2009	Toshiba American Medical Systems Inc	2	Toshiba Infinix fluoroscopy DFP-8000D Digital Radiography System with version 3.40 or higher software. Controller for Infinix interventional angiography systems.
Z-0031-2007	AGFA Corp.	2	CR DX-S, Image Intensified Fluoroscopic X-ray system.
Z-0009-2015	Gendex Corp	2	eXpertDC intraoral x-ray, models: eXpert DC, NA, 75 Inch reach; eXpert DC, NA, 65 Inch reach; eXpert DC, CN, 55 Inch reach; eXpert DC, WW, 75 Inch reach; eXpert DC, WW, 65 Inch reach; eXpert DC, WW, 55 Inch reach; OEM Arm Assembly w/o cables; Assy, Articulated Arm & Tubehead, eDC; and Assy, Articulated Arm & Tubehead, 765DC Product Usage: intraoral x-ray
Z-0016-2017	Panoramic Rental Corp.	2	Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage: The PC-1000 will enable the user to take panoramic x-ray images. The PC-1000/Laser1000 will enable the user to take panoramic x-ray images as well as cephalometric x-ray images.
Z-0002-2009	GE Medical Systems, LLC	2	Revolution XR/d system control room PC model 5117866-2 with Software collector 5115434

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014209556. Last updated year: 2026. Please use registration number 3014209556 when referencing this establishment in official correspondence.