# Ecotron Co., Ltd.

- Location (FDA's records): Seoul, KR
- FDA decisions: 4 (2015–2022): 4 510(k) clearances
- Product codes: OWB (2), IZL (1), EHD (1)
- 510(k) review time since 2016: median 59 days, against 58 for FDA's reviews in the same codes and years (1 of 3 faster)
- Predicates its devices cite: 4 (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
- Job Corporation: 1 (https://510kreport.com/company/job)
- United Radiology Systems, Inc.: 1 (https://510kreport.com/company/united-radiology-systems)
- Aribex, Inc.: 1 (https://510kreport.com/company/aribex)

## Firms that cite its devices most
- Portavision Medical, LLC: 1 (https://510kreport.com/company/portavision-medical)
- PDX Co., Ltd.: 1 (https://510kreport.com/company/pdx)

## Its most-cited devices
- K160279: ANYVIEW-500R Fluoroscopic Mobile X-Ray System (2016), cited by 2
- K221233: DT-703 (2022), cited by 1

## Recent decisions
- K221233: DT-703 (Jun 27, 2022)
- K180473: ANYVIEW DR SERIES FPD Fluoroscopic Mobile C-arm ANYVIEW-240DR, ANYVIEW-320DR, ANYVIEW-500DR (Mar 23, 2018)
- K160279: ANYVIEW-500R Fluoroscopic Mobile X-Ray System (Oct 14, 2016)
- K151038: EPX-Series Mobile X-ray System (Jul 24, 2015)

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