K252246
- 510(k) number
- K252246
- Device name
- Leforte MMF System
- Applicant
- Jeil Medical Corporation KR
- Product code
- JEY — Plate, Bone
- Decision date
- 2026-04-02
- Date received
- 2025-07-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.6 MB · U.S. public domain
Also available from FDA: K252246.pdf
Official FDA record: K252246
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.