# Livermoretech, Inc.

- Location (FDA's records): Plano, TX
- FDA decisions: 6 (2018–2025): 6 510(k) clearances
- Product codes: IZL (2), OWB (1), KPR (1), EHD (1), MQB (1)
- 510(k) review time since 2016: median 114 days, against 48 for FDA's reviews in the same codes and years (1 of 6 faster)
- Predicates its devices cite: 5 (1 its own); citations of its devices by later devices: 3 (1 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- United Radiology Systems, Inc.: 1 (https://510kreport.com/company/united-radiology-systems)
- Aribex, Inc.: 1 (https://510kreport.com/company/aribex)
- Dexcowin Co., Ltd.: 1 (https://510kreport.com/company/dexcowin)
- Sedecal., Sa.: 1 (https://510kreport.com/company/sedecal)

## Firms that cite its devices most
- Energy Resources International Co., Ltd.: 1 (https://510kreport.com/company/energy-resources-international)
- First Source, Inc.: 1 (https://510kreport.com/company/first-source)

## Its most-cited devices
- K193535: EZER, Portable X-ray System (2020), cited by 2
- K193644: E-Com DR-2000 DR (2020), cited by 1

## Recent decisions
- K244049: Europa (Alternative: AiRTouch) portable X-ray system (May 28, 2025)
- K193535: EZER, Portable X-ray System (May 7, 2020)
- K200022: FLUSION-9001, Fluoroscopic C-arm Mobile X-ray System (Apr 3, 2020)
- K193644: E-Com DR-2000 DR (Feb 14, 2020)
- K190935: EZER, Portable X-ray System (Dec 19, 2019)
- K180663: LaVid FMTS DIAGNOSTIC X-RAY SYSTEM (May 18, 2018)

Source page: https://510kreport.com/company/livermoretech