FDA applicant

Four Directions

Seattle, WA1 decision1993–19930 recalls

FDA records 1 decision for Four Directions (Seattle, WA) in 1993: 1 510(k) clearance. All are in product code LYG (Massager, Therapeutic, Manual). 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 Four Directions’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Four Directions since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Four Directions’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Four Directions

Which product codes does it file in?

What has FDA decided for it lately?