K260661
- 510(k) number
- K260661
- Device name
- Midas Restore
- Applicant
- Sprintray, Inc. CA · US
- Product code
- EBF — Material, Tooth Shade, Resin
- Decision date
- 2026-04-15
- Date received
- 2026-03-02
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K260661.pdf
Official FDA record: K260661
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.