Leone S.P.A.
FDA Regulatory Profile
Leone S.P.A. appears in FDA public data with 0 recalls, 4 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 19, 2025.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K242944 | Leone Orthodontic Implant TAD (Temporary Anchorage Device) | June 19, 2025 |
| K071490 | LEONE ORTHODONTIC MINI IMPLANT | February 22, 2008 |
| K070483 | LEONE MONOIMPLANT FOR O-RING OVERDENTURE | April 19, 2007 |
| K050586 | LEONE IMPLANT SYSTEM | February 27, 2006 |