510(k) Report

FDA applicant

Xinkang Medical Instrument Co., Ltd.

Shenzhen, CN2 decisions2020–20200 recalls

FDA records 2 decisions for Xinkang Medical Instrument Co., Ltd. (Shenzhen, CN) in 2020: 2 510(k) clearances. Most are in product codes DSA (Cable, Transducer And Electrode, Patient…) and DQA (Oximeter). 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, cardiovascular panel, where it files most

How often FDA has decided Xinkang Medical Instrument Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

2in 2020

2020: 2
2020high 2 (2020) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2020.

FIG. 1 — Xinkang Medical Instrument Co., Ltd. by year, 2020–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • DSACable, Transducer And Electrode, Patient, (Including Connector)1decision
  • DQAOximeter1decision

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 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.

  • K201360Reusable and Disposable SpO2 SensorsXinkang Medical Instrument Co., Ltd. · 20201cites it

What has FDA decided for it lately?

  • K201359ECG Cables and LeadwiresXinkang Medical Instrument Co., Ltd. · 2020
  • K201360Reusable and Disposable SpO2 SensorsXinkang Medical Instrument Co., Ltd. · 2020

All 2 as Xinkang Medical Instrument Co., Ltd. →