510(k) Report

FDA applicant

Grad-Line Corp.

Deerfield, FL1 decision1998–19980 recalls

FDA records 1 decision for Grad-Line Corp. (Deerfield, FL) in 1998: 1 510(k) clearance. All are in product code IRP (Massager, Powered Inflatable Tube). 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 Grad-Line Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Grad-Line Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • IRPMassager, Powered Inflatable Tube1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K974395Atlant'sGrad-Line Corp. · 19981cites it

What has FDA decided for it lately?

  • K974395Atlant'sGrad-Line Corp. · 1998

The one decision as Grad-Line Corp. →