510(k) Report

FDA applicant

Back IN Action, Inc.

Mountain View, CA2 decisions1989–19890 recalls

FDA records 2 decisions for Back IN Action, Inc. (Mountain View, CA) in 1989: 2 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and ISA (Massager, Therapeutic, Electric). 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 IN Action, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Back IN Action, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Back IN Action, Inc. 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.