Joylux

GUDID 00850012528364

Let's Spin Intimacy Gel

Joylux, Inc.

Sexual lubricant

• Primary Device ID: 00850012528364
• NIH Device Record Key: 46e70cdb-24de-499b-aea3-635349bef0c0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Joylux
• Version Model Number: JLD107
• Company DUNS: 079956040
• Company Name: Joylux, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850012528364 [Primary]
GS1	10850012528361 [Package]; Package: [24 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K242958

FDA Product Code

• NUC: Lubricant, Personal

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-31
• Device Publish Date: 2026-03-23

On-Brand Devices [Joylux]

• 00850012528463: Mini LET’S SPIN™ Intimacy Gel 1.35oz
• 00850012528364: Let's Spin Intimacy Gel