510(k) Report

FDA applicant

Kdb Inc. (Dba) Sperti Sunlamp

Crescent Springs, KY1 decision2018–20180 recalls

FDA records 1 decision for Kdb Inc. (Dba) Sperti Sunlamp (Crescent Springs, KY) in 2018: 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 Kdb Inc. (Dba) Sperti Sunlamp’s devices, and how often a recall has named them.

FDA decisions per year

1in 2018

2018: 1
2018high 1 (2018) · low 0 (2019)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2018.

FIG. 1 — Kdb Inc. (Dba) Sperti Sunlamp by year, 2018–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Kdb Inc. (Dba) Sperti Sunlamp’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • LEJBooth, Sun Tan1decision

What has FDA decided for it lately?

  • K151721Fiji Sun Fluorescent Tanning UnitKdb Inc. (Dba) Sperti Sunlamp · 2018

The one decision as Kdb Inc. (Dba) Sperti Sunlamp →