FDA applicant

Mottek Intl. Corp.

Scottsdale, AZ9 decisions1980–19860 recalls

FDA records 9 decisions for Mottek Intl. Corp. (Scottsdale, AZ) from 1980 to 1986: 9 510(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 Mottek Intl. Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mottek Intl. Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Mottek Intl. Corp.

Which product codes does it file in?

What has FDA decided for it lately?