FDA applicant

Ferno Ille-Forge

Williamsport, PA1 decision1988–19880 recalls

FDA records 1 decision for Ferno Ille-Forge (Williamsport, PA) in 1988: 1 510(k) clearance. 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 Ferno Ille-Forge’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ferno Ille-Forge since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ferno Ille-Forge’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 “Ferno”

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

Ferno-Washington, Inc. 5 Ferno 5 Ferno Ille 1

Ferno Ille-Forge

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Ferno”