Aidite Pmma Multilayer
by Aidite (Qinhuangdao) Technology Co., Ltd. 185 variants
Aidite Pmma Multilayer is a Class II device made by Aidite (Qinhuangdao) Technology Co., Ltd., cleared under FDA 510(k) K190217 on 17 Dec 2020 and listed in FDA GUDID since 10 Apr 2022 (UDI-DI 06934906676639), active as of 22 Oct 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 | Number06934906676639 | Date10 Apr 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK190217 | Date17 Dec 2020 | StatusActive |
Official records
- AccessGUDID record 06934906676639
- FDA 510(k) database K190217
Across registries
- FDA 510(k) K190217 decided 17 Dec 2020 Active
- FDA GUDID UDI-DI 06934906676639 listed 10 Apr 2022 Listed
Timeline
- Cleared FDA 510(k) K190217
- Listed FDA GUDID 06934906676639
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Aidite Pmma
- Generic name
- Dental appliance fabrication material, ceramic
- Model / reference
- Multilayer
- Primary DI / UDI-DI
- 06934906676639
- 510(k) Number
- FDA product code
- EBG
- GMDN term
- Dental appliance fabrication material, ceramic
- Device class
- Class II
- Regulation number
- 872.3770
- GUDID distribution status
- In Commercial Distribution
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