510(k) Report

FDA applicant

Blv Licht-Und Vakuumtechnik GmbH

Steinhoring, DE1 decision2016–20160 recalls

FDA records 1 decision for Blv Licht-Und Vakuumtechnik GmbH (Steinhoring, DE) in 2016: 1 510(k) clearance. All are in product code LEJ (Booth, Sun Tan). No recall is linked to its devices.

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

FIG. A — Illustration, general and plastic surgery panel, where it files most

How often FDA has decided Blv Licht-Und Vakuumtechnik GmbH’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016: 1
2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Blv Licht-Und Vakuumtechnik GmbH by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • LEJBooth, Sun Tan1decision

What has FDA decided for it lately?

  • K152141High Pressure Tanning LampsBlv Licht-Und Vakuumtechnik GmbH · 2016

The one decision as Blv Licht-Und Vakuumtechnik GmbH →