FDA applicant

Folio Products, Inc.

Longmont, CO3 decisions1990–19910 recalls

FDA records 3 decisions for Folio Products, Inc. (Longmont, CO) from 1990 to 1991: 3 510(k) clearances. All are in product code ITI (Wheelchair, Powered). 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 Folio Products, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Folio Products, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Folio Products, Inc.

Which product codes does it file in?

What has FDA decided for it lately?