510(k) Report

FDA applicant

Conmo Electronic Company Limited

Shenzhen City, CN3 decisions2014–20210 recalls

FDA records 3 decisions for Conmo Electronic Company Limited (Shenzhen City, CN) from 2014 to 2021: 3 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and FLL (Continuous Measurement Thermometer). Its devices cite 3 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, cardiovascular panel, where it files most

How often FDA has decided Conmo Electronic Company Limited’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2014: 12020: 12021: 1
2014high 1 (2014) · low 0 (2015)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2014.

FIG. 1 — Conmo Electronic Company Limited by year, 2014–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DXNSystem, Measurement, Blood-Pressure, Non-Invasive1decision
  • FLLContinuous Measurement Thermometer1decision
  • MNWAnalyzer, Body Composition1decision

Whose devices does it build on?

Its devices cite 3 predicates; 0 are its own earlier devices. The firms it cites most:

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.

  • K202420Infrared Forehead ThermometerConmo Electronic Company Limited · 20211cites it

What has FDA decided for it lately?

  • K202420Infrared Forehead ThermometerConmo Electronic Company Limited · 2021
  • K202372Upper Arm Electronic Blood Pressure MonitorConmo Electronic Company Limited · 2020
  • K140594Body Fat Analyzer and ScaleConmo Electronic Company Limited · 2014

All 3 as Conmo Electronic Company Limited →