Seohancare Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Seohancare Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: MEGAFIX® Pedicle Screw Spinal System
1
Total
1
Cleared
0
Denied
Seohancare Co., Ltd. has 1 FDA 510(k) cleared medical devices. Based in Gimpo-Si, KR.
Historical record: 1 cleared submissions from 2020 to 2020. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Seohancare Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Seohancare Co., Ltd.
1 devices