K233231
- 510(k) number
- K233231
- Device name
- Dental Implants and Abutments
- Applicant
- Ditron Dental, Ltd. IL
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2024-04-30
- Date received
- 2023-09-28
- 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: K233231.pdf
Official FDA record: K233231
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.