rainbowTM Paste Stain PS-Brown (5g)
by Genoss
rainbowTM Paste Stain PS-Brown (5g) is a Class II device made by Genoss, cleared under FDA 510(k) K151731 on 15 Apr 2016 and listed in FDA GUDID since 10 Jul 2018 (UDI-DI 08809324766416), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08809324766416 | Date10 Jul 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK151731 | Date15 Apr 2016 | StatusActive |
Official records
- AccessGUDID record 08809324766416
- FDA 510(k) database K151731
Across registries
- FDA 510(k) K151731 decided 15 Apr 2016 Active
- FDA GUDID UDI-DI 08809324766416 listed 10 Jul 2018 Listed
Timeline
- Cleared FDA 510(k) K151731
- Listed FDA GUDID 08809324766416
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- rainbowTM Paste Stain
- Generic name
- Dental appliance fabrication material, ceramic
- Model / Ref / Catalog
- PS-Brown (5g)
- Primary DI / UDI-DI
- 08809324766416
- 510(k) Number
- FDA product code
- EIH
- GMDN term
- Dental appliance fabrication material, ceramic
- Device class
- Class II
- Regulation number
- 872.6660
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Radiation Sterilization
- Size
- Weight — 5 Gram
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