K242072
- 510(k) number
- K242072
- Device name
- CeraRoot TL Implant System (TL)
- Applicant
- Ceraroot SL ES
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2025-05-14
- Date received
- 2024-07-16
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K242072.pdf
Official FDA record: K242072
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.