FDA applicant

Far Orthopedics, Inc.

Canada, CA2 decisions1984–19860 recalls

FDA records 2 decisions for Far Orthopedics, Inc. (Canada, CA) from 1984 to 1986: 2 510(k) clearances. Most are in product codes LDK (Device, Sensing, Optical Contour) and LYH (Arthrometer). 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 Far Orthopedics, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Far Orthopedics, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Far Orthopedics, Inc.

Which product codes does it file in?

What has FDA decided for it lately?