Livermoretech, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Livermoretech, Inc. has 6 FDA 510(k) cleared medical devices. Based in Plano, US.
Latest FDA clearance: May 2025. Active since 2018. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Livermoretech, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mtech Group, LLC as regulatory consultant.
6 devices
Cleared
May 28, 2025
Europa (Alternative: AiRTouch) portable X-ray system
Radiology
148d
Cleared
May 07, 2020
EZER, Portable X-ray System
Radiology
139d
Cleared
Apr 03, 2020
FLUSION-9001, Fluoroscopic C-arm Mobile X-ray System
Radiology
88d
Cleared
Feb 14, 2020
E-COM DR-2000 DR
Radiology
46d
Cleared
Dec 19, 2019
EZER, Portable X-ray System
Radiology
253d
Cleared
May 18, 2018
LaVid FMTS DIAGNOSTIC X-RAY SYSTEM
Radiology
65d