510(k) Report

FDA applicant

Dermatron Corp.

Mchenry, IL5 decisions1976–19770 recalls

FDA records 5 decisions for Dermatron Corp. (Mchenry, IL) from 1976 to 1977: 5 510(k) clearances. Most are in product codes FTC (Light, Ultraviolet, Dermatological) and IOB (Lamp, Infrared, Non Heating). 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 Dermatron Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dermatron Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Dermatron Corp.’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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