PeriOptix® A-REPKIT-NA
PeriOptix® A-REPKIT-NA is a Class I device made by Den-Mat Holdings, LLC, listed in FDA GUDID since 22 Sep 2022 (UDI-DI D813AREPKITNA0), 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 | NumberD813AREPKITNA0 | Date22 Sep 2022 | 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- Withdrawn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-REPKIT-NA
- Primary DI / UDI-DI
- D813AREPKITNA0
- FDA product code
- HOY
- GMDN term
- LED dental light, battery-powered
- Device class
- Class I
- Regulation number
- 886.4750
- GUDID distribution status
- In Commercial Distribution
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