K252890
- 510(k) number
- K252890
- Device name
- ZenSeal Pro
- Applicant
- Kerr Corporation CA · US
- Product code
- KIF — Resin, Root Canal Filling
- Decision date
- 2026-01-07
- Date received
- 2025-09-11
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Dental
PDFDownload 510(k) SummaryArchived here · 0.5 MB · U.S. public domain
Also available from FDA: K252890.pdf
Official FDA record: K252890
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.