VitaVitro LD-1.0
by Shenzhen Vitavitro Bio-Tech Co., Ltd.
VitaVitro LD-1.0 is an assisted reproduction vitrification kit (FDA Class II; FDA product code MQL, Media, Reproductive) made by Shenzhen Vitavitro Bio-Tech Co., Ltd., cleared under FDA 510(k) K180073 on 29 Aug 2018 and listed in FDA GUDID since 5 Dec 2018 (UDI-DI 06971982050014), 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 | Number06971982050014 | Date5 Dec 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK180073 | Date29 Aug 2018 | StatusActive |
Official records
- AccessGUDID record 06971982050014
- FDA 510(k) database K180073
Across registries
- FDA 510(k) K180073 decided 29 Aug 2018 Active
- FDA GUDID UDI-DI 06971982050014 listed 5 Dec 2018 Listed
Timeline
- Cleared FDA 510(k) K180073
- Listed FDA GUDID 06971982050014
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- VitaVitro
- Generic name
- Assisted reproduction vitrification kit
- Model / Ref / Catalog
- LD-1.0, V002001, V002002
- Primary DI / UDI-DI
- 06971982050014
- 510(k) Number
- FDA product code
- MQL
- GMDN term
- Assisted reproduction vitrification kit
- Device class
- Class II
- Regulation number
- 884.6180
- GUDID distribution status
- In Commercial Distribution
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