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/ Zmi Electronics , Ltd.
Zmi Electronics , 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
K241862
Levina Pelvic Floor Muscle Stimulator (RS-48)
March 27, 2025
K231166
Levina, Levina Incontinence Stimulation Electrodes (Sterile), Pelvic Floor Muscle Probe Electrodes
January 18, 2024
K180865
ZMI Self-Adhesive Electrodes
June 28, 2018