K242458
- 510(k) number
- K242458
- Device name
- ArgenZ MTZ
- Applicant
- Argen Corporation CA · US
- Product code
- EIH — Powder, Porcelain
- Decision date
- 2024-10-24
- Date received
- 2024-08-19
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
510(k) Summary (official FDA PDF): K242458.pdf
Official FDA record: K242458
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.