Data / Medical devices / United States / Valencia Naturals, Inc
Valencia Naturals, Inc: FDA-registered device maker in Chatsworth, CA, United States, 2 510(k) clearances
Valencia Naturals, Inc is registered with the FDA (registration 3013441423) in Chatsworth, CA, United States. It lists 1 device type. The FDA files 2 510(k) clearances under its listings, the newest dated April 13, 2022. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3013441423
- Address
- 9731 Topanga Canyon Place, Chatsworth, CA, United States, 91311
- Owner or operator
- Valencia Naturals, Inc. (10080561)
- Roles
- Specification developer
- First device listed
- February 11, 2021
- Registered through
- 2026
- Brand names listed
- Erolube, Sensuva Apple Candy Personal Lubricant, Sensuva Blueberry Muffin Personal Lubricant, Sensuva Butter Rum Personal Lubricant, Sensuva Cotton Candy Personal Lubricant, Sensuva Orange Creamsicle Personal Lubricant, Sensuva Salted Caramel Personal Lubricant, Sensuva Silicone Personal Lubricant and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lubricant, Personal | NUC | 2 | Specification developer | 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 |
|---|---|---|---|---|---|---|
| April 13, 2022 | K212260 | Sensuva Premium Silicone Personal Lubricant | NUC | Substantially Equivalent | Valencia Naturals, Inc. | accessdata.fda.gov |
| November 19, 2019 | K192204 | Sensuva Strawberry Personal Lubricant, Sensuva Apple Candy Personal Lubricant, Sensuva Butter Rum Personal Lubricant, Sensuva Orange Creamsicle Personal Lubricant, Sensuva Salted Caramel Personal Lubricant, | NUC | Substantially Equivalent | Valencia Naturals, Inc. | accessdata.fda.gov |
Compare with other makers
Updated April 13, 2022. 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.