Data / Medical devices / United States / Livermoretech,inc

Livermoretech,inc: FDA-registered device maker in Plano, TX, United States, 8 510(k) clearances

Name: Livermoretech,inc FDA registration, clearances, approvals and recalls
Creator: SpecStream
License: https://creativecommons.org/licenses/by/4.0/

Livermoretech,inc is registered with the FDA (registration 3014209556) in Plano, TX, United States. It lists 7 device types. The FDA files 8 510(k) clearances under its listings, the newest dated May 28, 2025. Registered through 2026. FDA data exported November 2, 2026.

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FDA registration number: 3014209556
Address: 801 north Jupiter rd suite 200, Plano, TX, United States, 75074
Owner or operator: LIVERMORETECH,INC (10056565)
Roles: Complaint file establishment, Manufacturer, Remanufacturer, Repackager or relabeler
First device listed: December 21, 2017
Registered through: 2026
Brand names listed: AIRTOUCH, PORTABLE X-RAY SYSTEM; EUROPA, PORTABLE X-RAY SYSTEM; EZER, PORTABLE X-RAY SYSTEM, AIRTOUCH, PORTABLE X-RAY SYSTEM; EZER, PORTABLE X-RAY SYSTEM, AspenXDR; ELIN-T4; SF-90C, DS-90; VB-90, EUROPA85, EUROPA85L, EUROPA90, EUROPA90L- Portable X-Ray System, LMT1417W, LMT1717W, SYSTEM, X-RAY, STATIONARY, SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER) and more

Devices it lists

Device	Product code	Class	Role	Source
Holder, Radiographic Cassette, Wall-Mounted	IXY	1	Manufacturer, Remanufacturer, Repackager or relabeler	accessdata.fda.gov
Solid State X-Ray Imager (Flat Panel/Digital Imager)	MQB	2	Repackager or relabeler	accessdata.fda.gov
System, X-Ray, Mobile	IZL	2	Complaint file establishment, Manufacturer	accessdata.fda.gov
System, X-Ray, Stationary	KPR	2	Repackager or relabeler	accessdata.fda.gov
Table, Radiologic	KXJ	2	Manufacturer, Remanufacturer, Repackager or relabeler	accessdata.fda.gov
Tube Mount, X-Ray, Diagnostic	IYB	1	Manufacturer	accessdata.fda.gov
Unit, X-Ray, Extraoral With Timer	EHD	2	Manufacturer	accessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided	510(k) number	Device	Product code	Decision	Applicant	Source
May 28, 2025	K244049	Europa (Alternative: AiRTouch) portable X-ray system	IZL	Substantially Equivalent	Livermoretech, Inc.	accessdata.fda.gov
May 12, 2020	K201043	Wireless Digital Flat Panel Detector (Model: Mars1717V-VSI, Mano4343W)	MQB	Substantially Equivalent	Iray Technology Taicang , Ltd.	accessdata.fda.gov
May 7, 2020	K193535	EZER, Portable X-ray System	IZL	Substantially Equivalent	Livermoretech, Inc.	accessdata.fda.gov
May 1, 2020	K201004	Wireless Digital Flat Panel Detector Model Name Mars1417V-TSI, Wireless Digital Flat Panel Detector Model Name Mano4336W	MQB	Substantially Equivalent	Iray Technology Taicang , Ltd.	accessdata.fda.gov
December 19, 2019	K190935	EZER, Portable X-ray System	EHD	Substantially Equivalent	Livermoretech, Inc.	accessdata.fda.gov
January 9, 2019	K183713	Wireless Digital Flat Detector	MQB	Substantially Equivalent	Iray Technology Taicang , Ltd.	accessdata.fda.gov
October 17, 2018	K182551	Wireless Digital Flat Panel Detector	MQB	Substantially Equivalent	Iray Technology Taicang , Ltd.	accessdata.fda.gov
May 8, 2015	K150816	Jumong Series	KPR	Substantially Equivalent	Sg Healthcare Co, Ltd.	accessdata.fda.gov

Compare with other makers

Updated May 28, 2025. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.