Sdjmastervision MVD01
by Tianjin Mastervision Technology Co., Ltd.
Sdjmastervision MVD01 is a Class II device made by Tianjin Mastervision Technology Co., Ltd., cleared under FDA 510(k) K241398 on 22 Oct 2024 and listed in FDA GUDID since 21 Jan 2025 (UDI-DI 06974939049000), 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 | Number06974939049000 | Date21 Jan 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK241398 | Date22 Oct 2024 | StatusActive |
Official records
- AccessGUDID record 06974939049000
- FDA 510(k) database K241398
Across registries
- FDA 510(k) K241398 decided 22 Oct 2024 Active
- FDA GUDID UDI-DI 06974939049000 listed 21 Jan 2025 Listed
Timeline
- Cleared FDA 510(k) K241398
- Listed FDA GUDID 06974939049000
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Sdjmastervision
- Generic name
- Rigid-gas-permeable corrective contact lens, daily-wear, non-customized
- Model / reference
- MVD01
- Primary DI / UDI-DI
- 06974939049000
- 510(k) Number
- FDA product code
- HQD
- GMDN term
- Rigid-gas-permeable corrective contact lens, daily-wear, non-customized
- Device class
- Class II
- Regulation number
- 886.5916
- GUDID distribution status
- In Commercial Distribution
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