K233896
- 510(k) number
- K233896
- Device name
- JDentalCare Dental Implant System: JDEvolution; JDEvolution plus; JDIcon; JDIcon plus
- Applicant
- Jdentalcare Srl IT
- Product code
- DZE — Implant, Endosseous, Root-Form
- Decision date
- 2024-08-16
- Date received
- 2023-12-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K233896.pdf
Official FDA record: K233896
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.