FDA applicant

Acuderm, Inc.

Ft. Lauderdale, FL13 decisions1983–19940 recalls

FDA records 13 decisions for Acuderm, Inc. (Ft. Lauderdale, FL) from 1983 to 1994: 13 510(k) clearances. Most are in product codes JSJ (Culture Media, Selective And Non-Differential) and MDM (Instrument, Manual, Surgical, General Use). 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 Acuderm, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Acuderm, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Acuderm, Inc.

Which product codes does it file in?

What has FDA decided for it lately?