Litex 696
by Dentamerica
Litex 696 is a Class II device made by Dentamerica, cleared under FDA 510(k) K955759 on 2 Jan 1996 and listed in FDA GUDID since 5 Oct 2016 (UDI-DI 00858466005196), 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 | Number00858466005196 | Date5 Oct 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK955759 | Date2 Jan 1996 | StatusActive |
Official records
- AccessGUDID record 00858466005196
- FDA 510(k) database K955759
Across registries
- FDA 510(k) K955759 decided 2 Jan 1996 Active
- FDA GUDID UDI-DI 00858466005196 listed 5 Oct 2016 Listed
Timeline
- Cleared FDA 510(k) K955759
- Listed FDA GUDID 00858466005196
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Litex
- Generic name
- Dental/surgical polymerization lamp
- Model / reference
- 696
- Primary DI / UDI-DI
- 00858466005196
- 510(k) Number
- FDA product code
- EBZ
- GMDN term
- Dental/surgical polymerization lamp
- Device class
- Class II
- Regulation number
- 872.6070
- GUDID distribution status
- In Commercial Distribution
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