Diamond D 1013017
Diamond D 1013017 is a Class II device made by Keystone Industries, cleared under FDA 510(k) K032773 on 23 Sep 2003 and listed in FDA GUDID since 15 Sep 2016 (UDI-DI H66810130171), 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 | NumberH66810130171 | Date15 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK032773 | Date23 Sep 2003 | StatusActive |
Official records
- FDA 510(k) database K032773
Across registries
- FDA 510(k) K032773 decided 23 Sep 2003 Active
- FDA GUDID UDI-DI H66810130171 listed 15 Sep 2016 Listed
Timeline
- Cleared FDA 510(k) K032773
- Listed FDA GUDID H66810130171
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Diamond D
- Generic name
- Dental appliance fabrication material, resin
- Model / Ref / Catalog
- 1013017
- Primary DI / UDI-DI
- H66810130171
- 510(k) Number
- FDA product code
- EBI
- GMDN term
- Dental appliance fabrication material, resin
- Device class
- Class II
- Regulation number
- 872.3760
- GUDID distribution status
- In Commercial Distribution
- Size
- Total Volume — 0.25 LiterTotal Volume — 8 Fluid Ounce
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