510(k) Report

FDA applicant

Tannhut

Mchenry, IL7 decisions1981–19850 recalls

FDA records 7 decisions for Tannhut (Mchenry, IL) from 1981 to 1985: 7 510(k) clearances. Most are in product codes FTC (Light, Ultraviolet, Dermatological) and 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 Tannhut’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tannhut since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tannhut by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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