FDA applicant

Back Rite

Walker, MI1 decision1981–19810 recalls

FDA records 1 decision for Back Rite (Walker, MI) in 1981: 1 510(k) clearance. All are in product code ION (Exerciser, Non-Measuring). 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 Back Rite’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Back Rite since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Back”

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

Back 2 Basics Direct, LLC 4 Back IN Action, Inc. 2 Back-On-Track, Inc. 1

Back Rite

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Back”