FDA applicant

Dermaphylyx, Inc.

Arvada, CO9 decisions1999–19990 recalls

FDA records 9 decisions for Dermaphylyx, Inc. (Arvada, CO) in 1999: 9 510(k) clearances. Most are in product codes KMF (Bandage, Liquid) and MGP (Dressing, Wound And Burn, Occlusive). 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 Dermaphylyx, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dermaphylyx, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Dermaphylyx, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?