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Xstrahl, Ltd.

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K240671XBeam (v2)December 4, 2024
K230611X80 / RADiant / PhotoElectric Therapy System (RADiant Aura)July 13, 2023
K172080Photoelectric Therapy SystemSeptember 29, 2017