K240725
- 510(k) number
- K240725
- Device name
- PreXolid CAD/CAM abutments
- Applicant
- Eclectic Co., Ltd. KR
- Product code
- NHA — Abutment, Implant, Dental, Endosseous
- Decision date
- 2024-10-18
- Date received
- 2024-03-18
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K240725.pdf
Official FDA record: K240725
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.