Nobilium 21102
Nobilium 21102 is a Class II device 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 M482211020), 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 | NumberM482211020 | 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 M482211020 listed 15 Nov 2016 Listed
Timeline
- Cleared FDA 510(k) K072402
- Listed FDA GUDID M482211020
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- Withdrawn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
- 21102
- Primary DI / UDI-DI
- M482211020
- 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.