510(k) Report

FDA applicant

Nemectron Medical, Inc.

Temecula, CA13 decisions1980–19930 recalls

FDA records 13 decisions for Nemectron Medical, Inc. (Temecula, CA) from 1980 to 1993: 13 510(k) clearances. Most are in product codes IPF (Stimulator, Muscle, Powered) and IMJ (Diathermy, Shortwave, For Use In Applying…). 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 Medical, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Nemectron Medical, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Nemectron”

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