K230242
- 510(k) number
- K230242
- Device name
- OsteoCentric Dental Implant System
- Applicant
- OsteoCentric Technologies UT · US
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2023-10-05
- Date received
- 2023-01-30
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K230242.pdf
Official FDA record: K230242
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.