Lovehoney Cherry 3.4oz
by Westridge Laboratories Incorporated
Lovehoney Cherry 3.4oz (IDD11350) is a Class II device made by Westridge Laboratories Incorporated, cleared under FDA 510(k) K051295 on 15 Feb 2006 and listed in FDA GUDID since 7 Apr 2023 (UDI-DI 05060493009862), 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 | Number05060493009862 | Date7 Apr 2023 | StatusListed |
| United States | FDA 510(k)SESE | NumberK051295 | Date15 Feb 2006 | StatusActive |
Official records
- AccessGUDID record 05060493009862
- FDA 510(k) database K051295
Across registries
- FDA 510(k) K051295 decided 15 Feb 2006 Active
- FDA GUDID UDI-DI 05060493009862 listed 7 Apr 2023 Listed
Timeline
- Cleared FDA 510(k) K051295
- Listed FDA GUDID 05060493009862
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Lovehoney Cherry
- Generic name
- Sexual lubricant
- Model / Ref / Catalog
- Lovehoney Cherry 3.4oz, IDD11350
- Primary DI / UDI-DI
- 05060493009862
- 510(k) Number
- FDA product code
- NUC
- GMDN term
- Sexual lubricant
- Device class
- Class II
- Regulation number
- 884.5300
- GUDID distribution status
- In Commercial Distribution
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