Aiobio Linkdens Vu
Aiobio Linkdens Vu is a Class I device made by AIOBIO Co., Ltd., listed in FDA GUDID since 10 Jul 2024 (UDI-DI 08800043200212), 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 | Number08800043200212 | Date10 Jul 2024 | StatusListed |
Official records
- AccessGUDID record 08800043200212
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Aiobio
- Generic name
- Fibreoptic dental light
- Model / reference
- LINKDENS VU
- Primary DI / UDI-DI
- 08800043200212
- FDA product code
- EAZ
- GMDN term
- Fibreoptic dental light
- Device class
- Class I
- Regulation number
- 872.4630
- GUDID distribution status
- In Commercial Distribution
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