LIGHT SOURCES, INC.

FDA Device Registration & Listing · ORANGE, CT, US · Registration 1221013

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
1221013
FEI Number
1221013
Entity Name
LIGHT SOURCES, INC.
City/State/Country
ORANGE, CT, US
Establishment Address
37 Robinson Blvd, ORANGE, CT 06477, US
Establishment Type(s)
Repack or Relabel Medical Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
LIGHT SOURCES, INC. (Owner Number: 1221013)
Owner / Operator Contact Address
37 ROBINSON BLVD., --, Orange, CT 06477, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
K151370
PMA Number
N/A

All Registered Proprietary Names

UV POWER HEX F74 SMART LAMP II BEAUTY LIGHT CLASSICS TAN AMERICA VIP GOLD SUN FUSION BRILLIANCE LET NEW TECHNOLOGY SUPRA D-UVF KBD PROSUN ESB SOLARA CLASSIC / REFRESH I XTREME ERGOLINE CHEETAH ESB TWIST POWER F71 100W TAN AMERICA VIP PRO SERIES ESB RENEW I TAN GENESIS SIGNATURE SERIES TANGO FABUTAN F71T12/HO ESB RXD-LITE AURORA PLANET TAN NEW COLORS I XCEL BERMUDA GOLD X POWER 2 TONE TWIST AUVL REAL SUN XS POW TWIST SUNMASTER HOLLYWOOD TAN ULTRA PALM BEACH I INTENSITY TAN AMERICA VIP PREMIER KALFASUN FIJI SUN ERS MEGALINE I BRONZE ESB SUNERGY RFL DUO SOLTRON ETERNAL SUN PLANET FITNESS SUNFIT PROTECH RAVE MAGIC SUN ESB SWIRL MAX RFL Light Sources General Sunlamp Series

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
LEJ Booth, Sun Tan General, Plastic Surgery Class 2 878.4635 2003-07-23
LEJ Booth, Sun Tan General, Plastic Surgery Class 2 878.4635 2020-02-27

Official Correspondent

Christian Imre

US Agent Details

No US Agent registered (Local establishment).

Related Public Records

Same Entity

LIGHT SOURCES, INC.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related 510(k) Records

510(k) Number Applicant Device Name Decision Date
K875190 Ultra Tan Intl. AB ULTRA TAN PURPLE PRO 1988-01-14

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 1221013. Last updated year: 2026. Please use registration number 1221013 when referencing this establishment in official correspondence.
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