510(k) Report

FDA applicant

Magnum Equipment LLC

Oklahoma City, OK1 decision2001–20010 recalls

FDA records 1 decision for Magnum Equipment LLC (Oklahoma City, OK) in 2001: 1 510(k) clearance. All are in product code JFB (Table, Physical Therapy, Multi Function). 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 Magnum Equipment LLC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Magnum Equipment LLC since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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

See the 510(k) Report

Which product codes does it file in?

  • JFBTable, Physical Therapy, Multi Function1decision

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.

  • K010252MagnumMagnum Equipment LLC · 20011cites it

What has FDA decided for it lately?

  • K010252MagnumMagnum Equipment LLC · 2001

The one decision as Magnum Equipment LLC →

Other applicant names beginning “Magnum”

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

Magnum Diamond, Inc. 2Magnum Instruments, Inc. 2Magnum Health and Safety Pvt, Ltd. 1