510(k) Report

510(k) · Cleared

Cleared

High Pressure Tanning Lamps

K152141510(k) TraditionalCleared Feb 25, 2016206-day reviewClass II21 CFR 878.4635

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Blv Licht-Und Vakuumtechnik GmbH · LEJ Booth, Sun Tan

Cleared on Feb 25, 2016 after a 206-day review. FDA’s file for it is a 510(k) statement, which names no predicate.

Decided
Feb 25, 2016
Review
206 days
Class
Class II
Product code
LEJ
Recalls
None
Predicates
0

FDA’s file for it is a 510(k) statement, which names no predicate.

FIG. 1 — Lineage of K152141Source: FDA 510(k) database · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

Sources: FDA 510(k) database (decision fields), the FDA 510(k) statement (indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.

Planning a device in LEJ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.

Top candidate predicates for a new LEJ device

  1. #1 K221523 Tanning Lampscore 5.2 · 2 generations · no Class I recall
  2. #2 Held for the reportin the report
Get a 510(k) Report

What was it cleared against?

FDA’s file for it is a 510(k) statement, which names no predicate.

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (0 Class I)

No FDA recall names this device.

No ancestor or descendant has a Class I recall.

How does its category compare?

All LEJ devices

LEJ Booth, Sun Tan: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.

FDA decisions per year · LEJ

1in 2023

2009: 12015: 92016: 112017: 12018: 62019: 32022: 12023: 1
2007high 11 (2016) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LEJ

105in 2019

2015: 102 days median2016: 247 days median2018: 106 days median2019: 105 days median
2007high 247 (2016) · low 102 (2015)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · LEJ

1in 2017

2017: 1
2007high 1 (2017) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · LEJ

1in 2025

2008: 12009: 12011: 22012: 292013: 42014: 92015: 42017: 92018: 42019: 12020: 32022: 42023: 22024: 22025: 1
2007high 29 (2012) · low 0 (2007)2025

MAUDE reports naming product code LEJ, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20070—00
20080—01
20091—01
20100—00
20110—02
20120—029
20130—04
20140—09
2015910204
20161124700
20171—19
2018610604
2019310501
20200—03
20210—00
20221—04
20231—02
20240—02
20250—01
20260—0—

What is it indicated for?

This ultraviolet lamp is intended for use in sunlamp products for tanning of the human skin

Indications for use read by OCR from a scanned FDA 510(k) statement, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K152141: High Pressure Tanning Lamps.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 3, 2026. https://510kreport.com/device/K152141

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

Record history
  • FDA decision record loaded May 2, 2026
  • Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
  • Page last updated Nov 3, 2026