PeriOptix A-LED6-99
PeriOptix A-LED6-99 is a Class I device made by Den-Mat Holdings, LLC, listed in FDA GUDID since 19 Sep 2024 (UDI-DI D813ALED6990), registry data as of 22 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 | NumberD813ALED6990 | Date19 Sep 2024 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- PeriOptix
- Generic name
- LED dental light, battery-powered
- Model / Ref / Catalog
- A-LED6-99
- Primary DI / UDI-DI
- D813ALED6990
- FDA product code
- KYT
- GMDN term
- LED dental light, battery-powered
- Device class
- Class I
- Regulation number
- 880.6350
- GUDID distribution status
- In Commercial Distribution
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