LensHooke Sperm Separation Device CA1 Package-25 sets-US-BR
LensHooke Sperm Separation Device CA1 Package-25 sets-US-BR is a sperm filtration system (FDA Class II; FDA product code MQK, Labware, Assisted Reproduction) made by Bonraybio Co., Ltd., cleared under FDA 510(k) K221810 on 31 Oct 2022 and listed in FDA GUDID since 16 Feb 2025 (UDI-DI 14719874742284), active as of 23 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 | Number14719874742284 | Date16 Feb 2025 | StatusListed |
| United States | FDA 510(k) | NumberK221810 | Date31 Oct 2022 | StatusActive |
Official records
- AccessGUDID record 14719874742284
- FDA 510(k) database K221810
Across registries
- FDA 510(k) K221810 decided 31 Oct 2022 Active
- FDA GUDID UDI-DI 14719874742284 listed 16 Feb 2025 Listed
Timeline
- Cleared FDA 510(k) K221810
- Listed FDA GUDID 14719874742284
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- LensHooke Sperm Separation Device
- Generic name
- Sperm filtration system
- Model / Ref / Catalog
- CA1 Package-25 sets-US-BR, CA1
- Primary DI / UDI-DI
- 14719874742284
- 510(k) Number
- FDA product code
- MQK
- GMDN term
- Sperm filtration system
- Device class
- Class II
- Regulation number
- 884.6160
- GUDID distribution status
- In Commercial Distribution
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