Pourable Db 072-50-0009
Pourable Db 072-50-0009 is a Class II device made by American Tooth Industries, listed in FDA GUDID since 18 Oct 2023 (UDI-DI D772ATI5000090), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | NumberD772ATI5000090 | Date18 Oct 2023 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Pourable Db
- Generic name
- Dental acrylic resin
- Model / reference
- 072-50-0009
- Primary DI / UDI-DI
- D772ATI5000090
- FDA product code
- EMA
- GMDN term
- Dental acrylic resin
- Device class
- Class II
- Regulation number
- 872.3275
- GUDID distribution status
- In Commercial Distribution
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