Data / Medical devices / United States / Light Sources, Inc.
Light Sources, Inc.: FDA-registered device maker in Orange, CT, United States, 1 510(k) clearance
Light Sources, Inc. is registered with the FDA (registration 1221013) in Orange, CT, United States. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated December 17, 2015. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 1221013
- Address
- 37 Robinson Blvd, Orange, CT, United States, 06477
- Owner or operator
- LIGHT SOURCES, INC. (1221013)
- Roles
- Repackager or relabeler, Specification developer
- First device listed
- July 23, 2003
- Registered through
- 2026
- Brand names listed
- AURORA, AUVL, BEAUTY LIGHT, BERMUDA GOLD, BRILLIANCE, CHEETAH, CLASSICS, D-UVF and more
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Booth, Sun Tan | LEJ | 2 | Repackager or relabeler, Specification developer | accessdata.fda.gov |
510(k) clearances
The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| December 17, 2015 | K151370 | UV Lamps for Indoor Tanning Devices | LEJ | Substantially Equivalent | Light Sources, Inc. | accessdata.fda.gov |
Compare with other makers
Updated December 17, 2015. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.