Rootloc Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Rootloc Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: Acculoc Total Knee System, Acculoc Total Knee System
2
Total
2
Cleared
0
Denied
Rootloc Co., Ltd. has 2 FDA 510(k) cleared medical devices. Based in Geumcheon-Gu, KR.
Historical record: 2 cleared submissions from 2018 to 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Rootloc Co., Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rootloc Co., Ltd.
2 devices