Data / Medical devices / United States / Live Well Brands, INC.
Live Well Brands, INC.: FDA-registered device maker in Ventura, CA, United States, 1 510(k) clearance
Live Well Brands, INC. is registered with the FDA (registration 3004089975) in Ventura, CA, United States. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated August 30, 2013. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3004089975
- Address
- 2568 Channel Dr Ste B, Ventura, CA, United States, 93003
- Owner or operator
- Live Well Brands (10045030)
- Roles
- Manufacturer, Repackager or relabeler
- First device listed
- September 16, 2013
- Registered through
- 2026
- Brand names listed
- APPLICATOR, VAGINAL, Aloe Cadabra Personal Lubricant - BEDEW, Aloe Cadabra Personal Lubricant - Banana Cream, Aloe Cadabra Personal Lubricant - Butter Rum, Aloe Cadabra Personal Lubricant - Candy Cane, Aloe Cadabra Personal Lubricant - Cherry Lemonade, Aloe Cadabra Personal Lubricant - Chocolate, Aloe Cadabra Personal Lubricant - French Lavender and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Applicator, Vaginal | HGD | 1 | Repackager or relabeler | accessdata.fda.gov |
| Lubricant, Personal | NUC | 2 | Manufacturer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| August 30, 2013 | K124044 | ALOE CADABRA LUBRICANT, ALOE CADABRA FLAVORED/SCENTED LUBRICANTS | NUC | Substantially Equivalent | Seven Oaks Ranch, Inc. | accessdata.fda.gov |
Compare with other makers
Updated August 30, 2013. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.