510(k) Report

FDA applicant

Freeman Procedure Seminars

Salem, OR1 decision1994–19940 recalls

FDA records 1 decision for Freeman Procedure Seminars (Salem, OR) in 1994: 1 510(k) clearance. All are in product code LXM (Manipulator, Plunger-Like Joint). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

How often FDA has decided Freeman Procedure Seminars’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Freeman Procedure Seminars since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Freeman Procedure Seminars 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?

  • LXMManipulator, Plunger-Like Joint1decision

Who builds on its devices?

Later devices cite its devices 3 times; 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.

  • K930431Arthrostim ManipulatorFreeman Procedure Seminars · 19943cite it

What has FDA decided for it lately?

  • K930431Arthrostim ManipulatorFreeman Procedure Seminars · 1994

The one decision as Freeman Procedure Seminars →