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/ Uzinmedicare Co., Ltd.
Uzinmedicare Co., Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K251423
Spectra S1 Pro; Spectra S2 Pro
February 6, 2026
K251932
Spectra Platinum
November 25, 2025
K220926
Spectra Wearable
December 12, 2022