510(k) Report

FDA applicant

Nemectron GmbH

Temecula, CA2 decisions1994–19940 recalls

FDA records 2 decisions for Nemectron GmbH (Temecula, CA) in 1994: 2 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and GZJ (Stimulator, Nerve, Transcutaneous, For Pain…). 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 Nemectron GmbH’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nemectron GmbH since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Nemectron GmbH 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?

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

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.

  • K932897Transcutaneous Electrical Nerve StimulatorNemectron GmbH · 19941cites it

What has FDA decided for it lately?

  • K932897Transcutaneous Electrical Nerve StimulatorNemectron GmbH · 1994
  • K932898Powered Muscle StimulatorNemectron GmbH · 1994

All 2 as Nemectron GmbH →

Other applicant names beginning “Nemectron”

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

Nemectron Medical, Inc. 13