510(k) Report

FDA applicant

Inarex Corporation

La Mirada, CA2 decisions2008–20100 recalls

FDA records 2 decisions for Inarex Corporation (La Mirada, CA) from 2008 to 2010: 2 510(k) clearances. All are in product code JFB (Table, Physical Therapy, Multi Function). Its devices cite 3 predicates, 1 of them its own earlier devices. 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 Inarex Corporation’s devices, and how often a recall has named them.

FDA decisions per year

1in 2010

2008: 12010: 1
2008high 1 (2008) · low 0 (2009)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2008.

FIG. 1 — Inarex Corporation by year, 2008–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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Which product codes does it file in?

  • JFBTable, Physical Therapy, Multi Function2decisions

Whose devices does it build on?

Its devices cite 3 predicates; 1 are its own earlier devices. The firms it cites most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K080554Inarex, Model 2D-LXInarex Corporation · 20081cites it

What has FDA decided for it lately?

  • K102281Thermal Massage Bed, Model 2D-GXInarex Corporation · 2010
  • K080554Inarex, Model 2D-LXInarex Corporation · 2008

All 2 as Inarex Corporation →