Ecotron Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Ecotron Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: DT-703, ANYVIEW DR SERIES FPD Fluoroscopic Mobile C-arm ANYVIEW-240DR, ANYVIEW-320DR, ANYVIEW-500DR
4
Total
4
Cleared
0
Denied
Ecotron Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Last cleared in 2022. Active since 2015. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Ecotron Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Mtechgroup as regulatory consultant.
FDA 510(k) Regulatory Record - Ecotron Co., Ltd.
4 devices
Cleared
Jun 27, 2022
DT-703
Radiology
59d
Cleared
Mar 23, 2018
ANYVIEW DR SERIES FPD Fluoroscopic Mobile C-arm ANYVIEW-240DR, ANYVIEW-320DR,...
Radiology
29d
Cleared
Oct 14, 2016
ANYVIEW-500R Fluoroscopic Mobile X-Ray System
Radiology
255d
Cleared
Jul 24, 2015
EPX-Series Mobile X-ray System
Radiology
95d