K251148
- 510(k) number
- K251148
- Device name
- JDEvolution Plus L and JDEvolution Plus LE
- Applicant
- Jdentalcare Srl IT
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2025-09-25
- Date received
- 2025-04-14
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.7 MB · U.S. public domain
Also available from FDA: K251148.pdf
Official FDA record: K251148
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.