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Livermoretech, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K244049Europa (Alternative: AiRTouch) portable X-ray systemMay 28, 2025
K193535EZER, Portable X-ray SystemMay 7, 2020
K200022FLUSION-9001, Fluoroscopic C-arm Mobile X-ray SystemApril 3, 2020
K193644E-COM DR-2000 DRFebruary 14, 2020
K190935EZER, Portable X-ray SystemDecember 19, 2019
K180663LaVid FMTS DIAGNOSTIC X-RAY SYSTEMMay 18, 2018