Lo 260-200-503
by Bicon, LLC
Lo 260-200-503 is a Class II device made by Bicon, LLC, cleared under FDA 510(k) K853788 on 31 Oct 1985 and listed in FDA GUDID since 1 Sep 2019 (UDI-DI 00813110028181), active as of 22 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 | Number00813110028181 | Date1 Sep 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK853788 | Date31 Oct 1985 | StatusActive |
Official records
- AccessGUDID record 00813110028181
- FDA 510(k) database K853788
Across registries
- FDA 510(k) K853788 decided 31 Oct 1985 Active
- FDA GUDID UDI-DI 00813110028181 listed 1 Sep 2019 Listed
Timeline
- Cleared FDA 510(k) K853788
- Listed FDA GUDID 00813110028181
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Lo
- Generic name
- Dental implant suprastructure, permanent, preformed
- Model / Ref / Catalog
- 260-200-503
- Primary DI / UDI-DI
- 00813110028181
- 510(k) Number
- FDA product code
- DZE
- GMDN term
- Dental implant suprastructure, permanent, preformed
- Device class
- Class II
- Regulation number
- 872.3640
- GUDID distribution status
- In Commercial Distribution
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