K252890 is an FDA 510(k) clearance for the ZenSeal Pro. This device is classified as a Resin, Root Canal Filling (Class II - Special Controls, product code KIF).
Submitted by Kerr Corporation (Pomona, US). The FDA issued a Cleared decision on January 7, 2026, 118 days after receiving the submission on September 11, 2025.
This device falls under the Dental FDA review panel. Regulated under 21 CFR 872.3820.
| 510(k) Number | K252890 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | September 11, 2025 |
| Decision Date | January 07, 2026 |
| Days to Decision | 118 days |
| Submission Type | Traditional |
| Review Panel | Dental (DE) |
| Summary | Summary PDF |
| Product Code | KIF — Resin, Root Canal Filling |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 872.3820 |