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Inbody Co., Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
2
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K231174
BPBIO750
August 2, 2023
K221764
InBody Blood pressure monitor, Model BPBIO480KV
October 7, 2022
K200560
InBody
January 6, 2021
K200442
InBody
December 4, 2020