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Indiba S. A. U.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K241107Indiba Diathermia Radiofrequency Deep Care Device (Deep care IDC0409/EVONY ); Indiba Diathermia RadJanuary 24, 2025
K243139Reverso Pro SystemJanuary 22, 2025
K243164INDIBA COMPACT devicesNovember 20, 2024