Livermoretech Inc

FDA Filings

This page includes the latest FDA filings for Livermoretech Inc. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3014209556
FEI Number3014209556
NameLIVERMORETECH,INC
Owner & OperatorLIVERMORETECH,INC
Contact Address801 north Jupiter rd suite 200
Plano TX 75074 US
Official Correspondent
  • JAY KIM
  • 1-214-2570113-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address801 north Jupiter rd suite 200
Plano, TX 75074 US
Establishment Type
  • Repack or Relabel Medical Device
  • Manufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Livermoretech Inc.
EZER, Portable X-ray System2020-05-07
LiverMoreTech Inc.
FLUSION-9001, Fluoroscopic C-arm Mobile X-ray System2020-04-03
LiverMoreTech, Inc.
E-COM DR-2000 DR2020-02-14
LIVERMORETECH,INC
EZER, PORTABLE X-ARY SYSTEM2019-12-23
LIVERMORETECH,INC
AIRTOUCH, PORTABLE X-ARY SYSTEM2019-12-23
Livermoretech Inc.
EZER, Portable X-ray System2019-12-19
LIVERMORETECH,INC
AspenXDR2018-05-21
LIVERMORETECH,INC
AspenUDR2018-05-21
LIVERMORETECH,INC
AspenFDR2018-05-21
LIVERMORETECH Inc.
LaVid FMTS DIAGNOSTIC X-RAY SYSTEM2018-05-18
LIVERMORETECH,INC
AspenXDR2017-12-21

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