FDA applicant

Dermarx Corp.

Denver, CO4 decisions1995–19970 recalls

FDA records 4 decisions for Dermarx Corp. (Denver, CO) from 1995 to 1997: 4 510(k) clearances. Most are in product codes KMF (Bandage, Liquid) and MGQ (Dressing, Wound And Burn, Hydrogel W/Drug…). 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 hospital panel, where it files most

How often FDA has decided Dermarx Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dermarx Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dermarx Corp.

Which product codes does it file in?

What has FDA decided for it lately?