Aidite
by Aidite (Qinhuangdao) Technology Co., Ltd. 406 variants
Aidite is a Class II device made by Aidite (Qinhuangdao) Technology Co., Ltd., cleared under FDA 510(k) K192723 on 18 Aug 2020 and listed in FDA GUDID since 8 Feb 2023 (UDI-DI 06976029566411), active as of 1 Jun 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number06976029566411 | Date8 Feb 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK192723 | Date18 Aug 2020 | StatusActive |
Official records
- AccessGUDID record 06976029566411
- FDA 510(k) database K192723
Across registries
- FDA 510(k) K192723 decided 18 Aug 2020 Active
- FDA GUDID UDI-DI 06976029566411 listed 8 Feb 2023 Listed
Timeline
- Cleared FDA 510(k) K192723
- Listed FDA GUDID 06976029566411
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Dental prosthesis dye
- Model / reference
- Aidite
- Primary DI / UDI-DI
- 06976029566411
- 510(k) Number
- FDA product code
- EIH
- GMDN term
- Dental prosthesis dye
- Device class
- Class II
- Regulation number
- 872.6660
- GUDID distribution status
- In Commercial Distribution
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