Luxator L3C
by Directa AB
Luxator L3C (506341U) is a Class I device made by Directa AB, listed in FDA GUDID since 7 Dec 2022 (UDI-DI 17310231050430), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number17310231050430 | Date7 Dec 2022 | StatusListed |
Official records
- AccessGUDID record 17310231050430
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Luxator
- Generic name
- Periotome, reusable
- Model / Ref / Catalog
- L3C, 506341U
- Primary DI / UDI-DI
- 17310231050430
- FDA product code
- EMJ
- GMDN term
- Periotome, reusable
- Device class
- Class I
- Regulation number
- 872.4565
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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