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Data / Medical devices / Booth, Sun Tan / United States

FDA-registered makers of Booth, Sun Tan in the United States: 7 establishments

7 establishments in the United States are registered with the FDA to make Booth, Sun Tan (product code LEJ). 7 have a 510(k) clearance or PMA approval on file and 1 has a recall event. FDA data exported November 2, 2026.

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Device
Booth, Sun Tan
Product code
LEJ
Country
United States

Makers of Booth, Sun Tan in the United States

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
JW North America, Inc.Rockland, MA, United StatesSpecification developer4October 30, 2015000api.fda.gov
Ibl Acquisitions LLCIndianapolis, IN, United StatesComplaint file establishment, Manufacturer, Specification developer3July 6, 2017000api.fda.gov
Sunshine USA, LLCJc, TN, United StatesManufacturer2April 19, 2018000api.fda.gov
J&T Health and Wellness LLCSaint Petersburg, FL, United StatesComplaint file establishment, Manufacturer1September 10, 2018030api.fda.gov
KBD, Inc.North Las Vegas, NV, United StatesSpecification developer1June 22, 2018000api.fda.gov
Light Sources, Inc.Orange, CT, United StatesRepackager or relabeler, Specification developer1December 17, 2015000api.fda.gov
Medtek Skin Care, Inc.Hudson Falls, NY, United StatesManufacturer1May 19, 2016000api.fda.gov

Updated November 2, 2026. 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.