Jeil Tech Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Jeil Tech Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Sterile Single-use LDV Syringe, CHOICARE Sterile Single-use LDV Syringe
1
Total
1
Cleared
0
Denied
Jeil Tech Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Sejong-Si, KR.
Last cleared in 2022. Active since 2022. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Jeil Tech Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Plusglobal as regulatory consultant.
FDA 510(k) Regulatory Record - Jeil Tech Co., Ltd.
1 devices