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ID Millennium, ID Moments Silicone Lubricant

by Westridge Laboratories, Inc.

510(k) K141767

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK141767 Date9 Mar 2015ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

Full name
Id Millennium, Id Moments Silicone
510(k) Number
FDA Product Code
NUC
Device Class
Class II
Regulation
21 CFR Part 884.5300
Advisory Committee
Obstetrics/Gynecology
FDA Decision
SESE Substantially Equivalent

Overview

AI-generated summary, 1 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The ID Millennium, ID Moments Silicone Lubricant is a silicone-based personal lubricant designed for intimate use. Classified as a lubricant under the FDA’s NUC (Non-Urological, Non-Cardiovascular) product code, it is intended to provide moisture and reduce friction during sexual activity. The product is formulated with hypoallergenic silicones and excludes glycerin, parabens, and other potential irritants, as noted in its specifications and regulatory submissions.

Supplied as a non-sterile, single-use product, the ID Millennium, ID Moments Silicone Lubricant is intended for over-the-counter consumer use. It is latex-compatible and designed for application during intimate activities. The device holds an FDA 510(k) clearance (K141767) under the Obstetrics/Gynecology advisory committee, with a classification as Class II. Multiple registration numbers (e.g., 3010409218) correspond to its regulatory filing under 21 CFR 884.5300. Storage and handling instructions are not specified in the data, but the product is intended for direct consumer application without sterilization.

Other devices from Westridge Laboratories, Inc.

Questions

AI-generated answers, 1 Oct 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

  • What is the ID Moments Silicone Lubricant designed for?

    The ID Moments Silicone Lubricant is specifically formulated as a silicone-based personal lubricant intended to provide moisture and reduce friction during intimate activities. Its hypoallergenic composition excludes common irritants like glycerin and parabens, making it suitable for sensitive skin.

  • How is the ID Moments Silicone Lubricant supplied and intended for use?

    This lubricant is supplied as a non-sterile, single-use product, designed exclusively for over-the-counter consumer use. It is meant for direct application during intimate activities and does not require sterilization before use.

  • Is the ID Moments Silicone Lubricant safe for latex users?

    Yes, the ID Moments Silicone Lubricant is explicitly labeled as latex-compatible. This means it can be safely used with latex condoms and other latex barriers without compromising their integrity.

  • What regulatory approval does the ID Moments Silicone Lubricant hold?

    The ID Moments Silicone Lubricant holds an FDA 510(k) clearance (K141767) under the Obstetrics/Gynecology advisory committee, classified as a Class II device. It is also filed under the FDA’s Non-Urological, Non-Cardiovascular (NUC) product code, ensuring it meets regulatory standards for personal lubricants.

  • Are there different sizes or models of the ID Moments Silicone Lubricant?

    The provided data does not specify distinct sizes or models beyond the single product line, ID Moments Silicone Lubricant. However, it is associated with multiple registration numbers, which may correspond to variations in packaging or batch production rather than differing product specifications.