FDA applicant

Heartland Tanning, Inc.

Lees Summit, MO1 decision2016–20160 recalls

FDA records 1 decision for Heartland Tanning, Inc. (Lees Summit, MO) 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 Heartland Tanning, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Heartland Tanning, Inc. by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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See the 510(k) Report

Other applicant names beginning “Heartland”

FDA records each applicant name separately; these may or may not be the same firm.

Heartland Health Products 1 Heartland Tan Systems 1 Heartland Medical Systems, Inc. 1

Heartland Tanning, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Heartland”