Aladdin
by Dxm Co., Ltd
Aladdin is a Class I device made by Dxm Co., Ltd, listed in FDA GUDID since 20 Jun 2023 (UDI-DI 08800017900049), registry data as of 8 Jun 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08800017900049 | Date20 Jun 2023 | StatusListed |
Official records
- AccessGUDID record 08800017900049
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Tooth-bleaching acceleration unit
- Model / reference
- Aladdin
- Primary DI / UDI-DI
- 08800017900049
- FDA product code
- EEG
- GMDN term
- Tooth-bleaching acceleration unit
- Device class
- Class I
- Regulation number
- 872.6475
- GUDID distribution status
- In Commercial Distribution
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