KJJ
- Product code
- KJJ
- Device name
- Cleanser, Root Canal
- Device class
- Class U
- Medical specialty
- Unknown
- Marketing pathway
- 510(K)
- 510(k) clearances (last 3 years)
- 2
- Summaries archived here
- 1 (direct download)
- 510(k) clearances (all years, FDA)
- 41 (all years; only the last 3 years are listed here)
510(k) clearances, last 3 years (2)
| Number | Decision date | Applicant | Device name | Summary |
|---|---|---|---|---|
| K250279 | 2025-07-02 | Belport Company, Inc., Gingi-Pak | RC-SwiftPrep | — |
| K241354 | 2024-08-27 | Inter-Med, Inc. | Sealer Solvent |
Official FDA classification page: KJJ
Classification and pathway per current FDA publications. Data from openFDA (CC0).