LOLA Personal Lubricant
LOLA Personal Lubricant is a Class II device made by Alyk, Inc., listed in FDA GUDID since 20 Jul 2020 (UDI-DI 00851617007667), registry data as of 22 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 | Number00851617007667 | Date20 Jul 2020 | StatusListed |
Official records
- AccessGUDID record 00851617007667
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Lola
- Generic name
- General-body orifice lubricant, non-sterile
- Model / reference
- Personal Lubricant
- Primary DI / UDI-DI
- 00851617007667
- FDA product code
- NUC
- GMDN term
- General-body orifice lubricant, non-sterile
- Device class
- Class II
- Regulation number
- 884.5300
- GUDID distribution status
- In Commercial Distribution
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