K231429
- 510(k) number
- K231429
- Device name
- S-Plant Dental Implant System
- Applicant
- Idis Co., Ltd. KR
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2023-12-18
- Date received
- 2023-05-17
- 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: K231429.pdf
Official FDA record: K231429
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.