510(k) Report

FDA applicant

Cefar Medical AB

Minneapolis,, MN2 decisions2002–20030 recalls

FDA records 2 decisions for Cefar Medical AB (Minneapolis,, MN) from 2002 to 2003: 2 510(k) clearances. Most are in product codes GZJ (Stimulator, Nerve, Transcutaneous, For Pain…) and IPF (Stimulator, Muscle, Powered). Its devices cite 2 predicates, 0 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, neurology panel, where it files most

How often FDA has decided Cefar Medical AB’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cefar Medical AB since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cefar Medical AB 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?

  • GZJStimulator, Nerve, Transcutaneous, For Pain Relief1decision
  • IPFStimulator, Muscle, Powered1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

Who builds on its devices?

Later devices cite its devices 2 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.

  • K020803Cefar Medical AB Cefar PrimoCefar Medical AB · 20022cite it

What has FDA decided for it lately?

  • K030403Cefar Rehab 2 and Rehab 2 ProCefar Medical AB · 2003
  • K020803Cefar Medical AB Cefar PrimoCefar Medical AB · 2002

All 2 as Cefar Medical AB →

Other applicant names beginning “Cefar”

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

Cefar Medical Products, Inc. 1