Joylux Intimacy Gel (PG3100)

FDA 510(k) K242958 · Joylux, Inc.

Substantially Equivalent

510(k) numberK242958

Submission

Device name
Joylux Intimacy Gel (PG3100)
Applicant
Joylux, Inc.
Seattle, WA, US
Received
September 25, 2024
Decision date
March 20, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
NUC – Lubricant, Personal
Device class
Class II (moderate risk)
Regulation
21 CFR 884.5300
Specialty
Obstetrics/Gynecology

This device is a personal lubricant, for penile and/or vaginal application, intended to moisturize and lubricate, to enhance the ease and comfort of intimate sexual activity, and supplement the body's natural lubrication. This product may or may not be compatible with natural rubber latex, polyisoprene, and/or polyurethane condoms.

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K261909Plum Vagiceuticals™ Vaginal Moisturizing SuppositoriesNUC · Traditional PCCA, Inc.07/06/2026SE
K254011Flow Water-Based Personal LubricantNUC · Traditional LBDO Group, Inc.06/22/2026SE
K261292PR Water-Base Lube Personal Lubricant (PR Water-Base Lube Personal Lubricant)NUC · Traditional PR Personal Care Laboratories06/11/2026SE
K252914Sutil Pure Personal Lubricant (models 1148, 1145, 1146, 1147)NUC · Traditional Hathor Professional Skincare , Ltd.06/09/2026SE
K260068pjur NATURE Touch, 100 mlNUC · Traditional Pjur Group Luxembourg S.A.05/21/2026SE
K254101Julva Velvé Water-Based Personal LubricantNUC · Traditional Golden Isles Medical, Inc.04/16/2026SE
K260007Hyaluronic Acid Vaginal Suppository (HA 5 mg); Hyaluronic Acid Vaginal Suppository (HA…NUC · Traditional Hudi Pharma Srl04/01/2026SE

Questions and answers

When was Joylux Intimacy Gel (PG3100) cleared by the FDA?

Joylux Intimacy Gel (PG3100) (K242958) received a 510(k) decision of Substantially Equivalent on March 20, 2025, 176 days after the submission was received.

What is the product code of K242958?

The FDA product code is NUC – Lubricant, Personal, a Class II (moderate risk) device regulated under 21 CFR 884.5300.