K221315
- 510(k) number
- K221315
- Device name
- UNIdental Symphony Implant System
- Applicant
- Unidental Co., Ltd. KR
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2023-10-25
- Date received
- 2022-05-06
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.8 MB · U.S. public domain
Also available from FDA: K221315.pdf
Official FDA record: K221315
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.