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Remedi Co., Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K240759
REMEX-GR100
May 13, 2024
K212144
Remex KA6
August 3, 2021
K200284
R-Sensor, R-Sensor
February 28, 2020