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Leone S.P.A.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
2
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K242944Leone Orthodontic Implant TAD (Temporary Anchorage Device)June 19, 2025
K071490LEONE ORTHODONTIC MINI IMPLANTFebruary 22, 2008
K070483LEONE MONOIMPLANT FOR O-RING OVERDENTUREApril 19, 2007
K050586LEONE IMPLANT SYSTEMFebruary 27, 2006