K241462
- 510(k) number
- K241462
- Device name
- LONGY Implant and LONGY-N Implant
- Applicant
- Noris Medical , Ltd. IL
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2025-02-11
- Date received
- 2024-05-23
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 2.8 MB · U.S. public domain
Also available from FDA: K241462.pdf
Official FDA record: K241462
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.