K233163
- 510(k) number
- K233163
- Device name
- ZENEX Implant System_Short
- Applicant
- Izenimplant Co., Ltd. KR
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2023-12-19
- Date received
- 2023-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 1.0 MB · U.S. public domain
Also available from FDA: K233163.pdf
Official FDA record: K233163
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.