Benilight iLED-Pro Mini
by Benilight
Benilight iLED-Pro Mini is a Class II device made by Benilight, listed in FDA GUDID since 1 Oct 2024 (UDI-DI 08809922440053), 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 | Number08809922440053 | Date1 Oct 2024 | StatusListed |
Official records
- AccessGUDID record 08809922440053
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Benilight
- Generic name
- Red/infrared light phototherapy unit
- Model / reference
- iLED-Pro Mini
- Primary DI / UDI-DI
- 08809922440053
- FDA product code
- ILY
- GMDN term
- Red/infrared light phototherapy unit
- Device class
- Class II
- Regulation number
- 890.5500
- GUDID distribution status
- In Commercial Distribution
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