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Ecotron Co., Ltd.

FDA Regulatory Profile

Ecotron Co., Ltd. has 0 FDA recalls, 0 inspections, 4 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jun 27, 2022

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances4Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K221233DT-703Jun 27, 2022
K180473ANYVIEW DR SERIES FPD Fluoroscopic Mobile C-arm ANYVIEW-240DR, ANYVIEW-320DR, ANYVIEW-500DRMar 23, 2018
K160279ANYVIEW-500R Fluoroscopic Mobile X-Ray SystemOct 14, 2016
K151038EPX-Series Mobile X-ray SystemJul 24, 2015

FDA data resources