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FDA 510(k)

Joylux Intimacy Gel (PG3100)

K-Number: K242958 · 2025-03-20

ApplicantJoylux, Inc.
Decision Date2025-03-20
Product CodeNUC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

Joylux Intimacy Gel (PG3100) is a medical device manufactured by Joylux, Inc.. It received FDA 510(k) clearance on 2025-03-20 under approval number K242958. The device is classified under product code NUC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Joylux Intimacy Gel (PG3100)?

Joylux Intimacy Gel (PG3100) is a medical device that received FDA 510(k) clearance on 2025-03-20. It is manufactured by Joylux, Inc.. The 510(k) number is K242958.

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

Joylux Intimacy Gel (PG3100) received FDA 510(k) clearance on 2025-03-20, under approval number K242958.

What company makes Joylux Intimacy Gel (PG3100)?

Joylux Intimacy Gel (PG3100) is manufactured by Joylux, Inc..

What is the FDA product code for Joylux Intimacy Gel (PG3100)?

The FDA product code for Joylux Intimacy Gel (PG3100) is NUC.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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