K251390
- 510(k) number
- K251390
- Device name
- MTA vpt
- Applicant
- Voco GmbH DE
- Product code
- KIF — Resin, Root Canal Filling
- Decision date
- 2025-07-03
- Date received
- 2025-05-05
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
This submission filed a 510(k) Statement rather than a Summary; no public summary is available from FDA.
Official FDA record: K251390
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.