FDA applicant

The Silcraft Corp.

Washington, DC2 decisions1998–19980 recalls

FDA records 2 decisions for The Silcraft Corp. (Washington, DC) in 1998: 2 510(k) clearances. All are in product code ILJ (Bath, Hydro-Massage). 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, physical medicine panel, where it files most

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

FDA decisions per year

No FDA decision for The Silcraft Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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The Silcraft Corp.

Which product codes does it file in?

What has FDA decided for it lately?