K232076
- 510(k) number
- K232076
- Device name
- Fibercure
- Applicant
- Lumendo AG CH
- Product code
- QNF — Laser Activator For Polymerization
- Decision date
- 2023-11-02
- Date received
- 2023-07-13
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K232076.pdf
Official FDA record: K232076
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.