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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 the device name listed in this FDA 510(k) record. The listed applicant is Joylux, Inc.. It received FDA 510(k) clearance on 2025-03-20 under 510(k) 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. The listed applicant is Joylux, Inc.. The 510(k) number is K242958.

When did Joylux Intimacy Gel (PG3100) receive FDA 510(k) clearance?

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

Who is the listed applicant for Joylux Intimacy Gel (PG3100)?

The FDA 510(k) record lists Joylux, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

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

Related Devices (Code: NUC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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