K233808
- 510(k) number
- K233808
- Device name
- LW Narrow Implant System
- Applicant
- Ossvis Co., Ltd. KR
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2024-07-31
- Date received
- 2023-11-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K233808.pdf
Official FDA record: K233808
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.