THE KAMA SUTRA COMPANY

FDA Device Registration & Listing · Moorpark, CA, US · Registration 1000375074

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1000375074
FEI Number
1000375074
Entity Name
THE KAMA SUTRA COMPANY
City/State/Country
Moorpark, CA, US
Establishment Address
5260 Kazuko Ct, Moorpark, CA 93021, US
Establishment Type(s)
Develop Specifications But Do Not Manufacture At This Facility,Repack or Relabel Medical Device
Owner / Operator
The Kama Sutra Company (Owner Number: 10054057)
Owner / Operator Contact Address
5260 Kazuko Ct, Moorpark, CA 93021, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K152168
PMA Number
N/A

All Registered Proprietary Names

LOVE LIQUID PERSONAL LUBRICANT

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
NUC Lubricant, Personal Obstetrics/Gynecology Class 2 884.5300 2017-02-07

Official Correspondent

Marla Lee

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

The Kama Sutra Company
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K050212 Qualis, Inc. PERSONAL WARMING JELLY 2005-03-17

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1000375074. Last updated year: 2026. Please use registration number 1000375074 when referencing this establishment in official correspondence.
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