FDA applicant

Bioderm, Inc.

Wheaton, IL14 decisions1987–19990 recalls

FDA records 14 decisions for Bioderm, Inc. (Wheaton, IL) from 1987 to 1999: 14 510(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 Bioderm, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bioderm, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Bioderm, Inc.’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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Other applicant names beginning “Bioderm”

FDA records each applicant name separately; these may or may not be the same firm.

Bioderm Sciences, Inc. 3

Bioderm, 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?

Other applicant names beginning “Bioderm”