Taebong Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Taebong Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: CottonDay Tampon
1
Total
1
Cleared
0
Denied
Taebong Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Gwangju Gwangyeogsi, KR.
Historical record: 1 cleared submissions from 2019 to 2019. Primary specialty: Obstetrics & Gynecology.
Browse the FDA 510(k) cleared devices submitted by Taebong Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Provision Consulting Group, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Taebong Co., Ltd.
1 devices