AURORA TANNING SYSTEMS

GUDID G5100751

Light Sources, Inc.

Ultraviolet tanning device
Primary Device IDG5100751
NIH Device Record Keyc24e8a36-626b-4cef-baf2-48916199157b
Commercial Distribution StatusIn Commercial Distribution
Brand NameAURORA TANNING SYSTEMS
Version Model Number0751
Company DUNS075058495
Company NameLight Sources, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCG5100751 [Primary]

FDA Product Code

LEJBooth, Sun Tan

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-06-13
Device Publish Date2025-06-05

On-Brand Devices [AURORA TANNING SYSTEMS]

G510070200702
G51007240FR71T12/BL/BP/6.5
G51007510751

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.