Nobilium 21112
Nobilium 21112 is a dental appliance fabrication material (FDA Class II; FDA product code EBI, Resin, Denture, Relining, Repairing, Rebasing) made by Cmp Industries LLC, cleared under FDA 510(k) K072402 on 19 Oct 2007 and listed in FDA GUDID since 15 Nov 2016 (UDI-DI M482211120), 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 | NumberM482211120 | Date15 Nov 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK072402 | Date19 Oct 2007 | StatusActive |
Official records
- FDA 510(k) database K072402
Across registries
- FDA 510(k) K072402 decided 19 Oct 2007 Active
- FDA GUDID UDI-DI M482211120 listed 15 Nov 2016 Listed
Timeline
- Cleared FDA 510(k) K072402
- Listed FDA GUDID M482211120
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Nobilium
- Generic name
- Dental appliance fabrication material, thermoplastic
- Model / reference
- 21112
- Primary DI / UDI-DI
- M482211120
- 510(k) Number
- FDA product code
- EBI
- GMDN term
- Dental appliance fabrication material, thermoplastic
- Device class
- Class II
- Regulation number
- 872.3760
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Dental appliance fabrication material, thermoplastic.