Aloe Cadabra BED.2APP
Aloe Cadabra BED.2APP is a vaginal lubricant (FDA Class II; FDA product code NUC, Lubricant, Personal) made by Live Well Brands, INC., cleared under FDA 510(k) K124044 on 30 Aug 2013 and listed in FDA GUDID since 17 Jun 2024 (UDI-DI 00826804006198), 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 | Number00826804006198 | Date17 Jun 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK124044 | Date30 Aug 2013 | StatusActive |
Official records
- AccessGUDID record 00826804006198
- FDA 510(k) database K124044
Across registries
- FDA 510(k) K124044 decided 30 Aug 2013 Active
- FDA GUDID UDI-DI 00826804006198 listed 17 Jun 2024 Listed
Timeline
- Cleared FDA 510(k) K124044
- Listed FDA GUDID 00826804006198
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Aloe Cadabra
- Generic name
- Vaginal lubricant
- Model / reference
- BED.2APP
- Primary DI / UDI-DI
- 00826804006198
- 510(k) Number
- FDA product code
- NUC
- GMDN term
- Vaginal lubricant
- Device class
- Class II
- Regulation number
- 884.5300
- GUDID distribution status
- In Commercial Distribution
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