Data / Medical devices / United States / The Kama Sutra Company
The Kama Sutra Company: FDA-registered device maker in Moorpark, CA, United States, 1 510(k) clearance
The Kama Sutra Company is registered with the FDA (registration 1000375074) in Moorpark, CA, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated February 5, 2016. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1000375074
- Address
- 5260 Kazuko Ct, Moorpark, CA, United States, 93021
- Owner or operator
- The Kama Sutra Company (10054057)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- February 7, 2017
- Registered through
- 2026
- Brand names listed
- LOVE LIQUID PERSONAL LUBRICANT
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Lubricant, Personal | NUC | 2 | Repackager or relabeler, 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 |
|---|---|---|---|---|---|---|
| February 5, 2016 | K152168 | Love Liquid Personal Lubricant | NUC | Substantially Equivalent | The Kama Sutra Company | accessdata.fda.gov |
Compare with other makers
Updated February 5, 2016. 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.