K241089
- 510(k) number
- K241089
- Device name
- KeyPrint KeyDenture Base
- Applicant
- Keystone Industries NJ · US
- Product code
- EBI — Resin, Denture, Relining, Repairing, Rebasing
- Decision date
- 2024-10-24
- Date received
- 2024-04-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K241089.pdf
Official FDA record: K241089
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.