Trilor FDC10
by Bioloren SRL
Trilor FDC10 is a Class II device made by Bioloren SRL, cleared under FDA 510(k) K173643 on 24 Feb 2018 and listed in FDA GUDID since 24 Mar 2018 (UDI-DI 08056099230776), 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 | Number08056099230776 | Date24 Mar 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK173643 | Date24 Feb 2018 | StatusActive |
Official records
- AccessGUDID record 08056099230776
- FDA 510(k) database K173643
Across registries
- FDA 510(k) K173643 decided 24 Feb 2018 Active
- FDA GUDID UDI-DI 08056099230776 listed 24 Mar 2018 Listed
Timeline
- Cleared FDA 510(k) K173643
- Listed FDA GUDID 08056099230776
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Trilor
- Generic name
- Dental implant suprastructure, permanent, preformed
- Model / reference
- FDC10
- Primary DI / UDI-DI
- 08056099230776
- 510(k) Number
- FDA product code
- EBF
- GMDN term
- Dental implant suprastructure, permanent, preformed
- Device class
- Class II
- Regulation number
- 872.3690
- GUDID distribution status
- In Commercial Distribution
- Size
- Height — 10 Millimeter
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