FACIAL SUNDASH

GUDID G5101213

Light Sources, Inc.

Ultraviolet tanning device

• Primary Device ID: G5101213
• NIH Device Record Key: a0b59e4b-9036-42bb-b024-453c5de02c8a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FACIAL SUNDASH
• Version Model Number: 1213
• Company DUNS: 075058495
• Company Name: Light Sources, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	G5101213 [Primary]

FDA Product Code

• LEJ: Booth, Sun Tan

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: 2025-08-15
• Device Publish Date: 2025-08-07

Devices Manufactured by Light Sources, Inc.

• G51033410 - RADIANCE: 2025-09-30
• G51033380 - RADIANCE: 2025-09-26
• G51033400 - RADIANCE: 2025-09-26
• G51032500 - REDSUN: 2025-09-25
• G51032650 - REDSUN: 2025-09-23
• G51031060 - MEGALINE: 2025-09-17
• G51033270 - RAVE RE-NEW: 2025-09-11
• G51033310 - RAVE RE-NEW: 2025-09-11