Zonn HL711 Pro Max
by Zonnsmart Science & Technology Co., Ltd
Zonn HL711 Pro Max is a Class II device made by Zonnsmart Science & Technology Co., Ltd, listed in FDA GUDID since 10 Sep 2024 (UDI-DI 06975188960139), 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 | Number06975188960139 | Date10 Sep 2024 | StatusListed |
Official records
- AccessGUDID record 06975188960139
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Zonn
- Generic name
- Red/infrared light phototherapy unit
- Model / reference
- HL711 PRO MAX
- Primary DI / UDI-DI
- 06975188960139
- 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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