Inbody Co., Ltd. is one of 351 FDA 510(k) medical device manufacturers from South Korea in the dataset, ranked by real submission volume.
Inbody Co., Ltd. - FDA 510(k) Cleared Devices
Recent clearances: BPBIO750, InBody Blood pressure monitor, Model BPBIO480KV, InBody
4
Total
4
Cleared
0
Denied
Inbody Co., Ltd. has 4 FDA 510(k) cleared medical devices. Based in Seoul, KR.
Last cleared in 2023. Active since 2020. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Inbody Co., Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Kamm & Associates as regulatory consultant.
FDA 510(k) Regulatory Record - Inbody Co., Ltd.
4 devices