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Elidah, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K253285Elitone for MenJanuary 23, 2026
K223884ELITONE Urge Urinary Incontinence DeviceFebruary 24, 2023
K183585Elitone DeviceFebruary 11, 2019