FDA.reportPublic FDA data

LIVERMORETECH,INC

FDA Registration(s)#

Registration, FEI, Name table
RegistrationFEINameStatusInitial importerExpiration yearAddress
30142095563014209556LIVERMORETECH,INC1N2026-01-01801 north Jupiter rd suite 200 Plano TX US 75074

Registered Device Listings#

Registration key, Listing key, Premarket submission table
Registration keyListing keyPremarket submissionDeviceProduct codeDecision date
2144481704523637K244049Europa (Alternative: AiRTouch) portable X-ray systemIZL2025-05-28
2144481355481111K201043Wireless Digital Flat Panel Detector (Model: Mars1717V-VSI, Mano4343W)MQB2020-05-12
2144481749095425K201004Wireless Digital Flat Panel Detector Model Name Mars1417V-TSI, Wireless Digital Flat Panel Detector Model Name Mano4336WMQB2020-05-01
2144481246904309K193535EZER, Portable X-ray SystemIZL2020-05-07
2144481109823436K190935EZER, Portable X-ray SystemEHD2019-12-19
2144481108934682K183713Wireless Digital Flat DetectorMQB2019-01-09
2144481460216335K182551Wireless Digital Flat Panel DetectorMQB2018-10-17
2144481154027763K180663LaVid FMTS DIAGNOSTIC X-RAY SYSTEMKPR2018-05-18
2144481310163448K150816Jumong SeriesKPR2015-05-08
2144482067838536
2144481300620376
2144481670926063

Product Codes Associated With Registrations#

Product code, Registration listing records, Latest decision table
Product codeRegistration listing recordsLatest decision
MQB42020-05-12
KPR32018-05-18
IZL22025-05-28
EHD22019-12-19

PMN#