rainbow Paste Stain SE
510(k) K233885
rainbow Paste Stain SE is a Class II device made by GENOSS CO., Ltd., cleared under FDA 510(k) K233885 on 21 Jun 2024, active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK233885 | Date21 Jun 2024 | StatusActive |
Official records
- FDA 510(k) database K233885
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- EIH
- Device class
- Class II
- Regulation
- 21 CFR Part 872.6660
- Advisory committee
- Dental
- FDA decision
- SESE Substantially Equivalent
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