510(k) Report

FDA applicant

Henan Tuoren Medical Device Co., Ltd.

Xinxiang, CN1 decision2016–20160 recalls

FDA records 1 decision for Henan Tuoren Medical Device Co., Ltd. (Xinxiang, CN) in 2016: 1 510(k) clearance. All are in product code CBI (Tube, Tracheal/Bronchial, Differential…). Its devices cite 1 predicate, 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, anesthesiology panel, where it files most

How often FDA has decided Henan Tuoren Medical Device Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2016: 1
2016high 1 (2016) · low 0 (2017)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2016.

FIG. 1 — Henan Tuoren Medical Device Co., Ltd. by year, 2016–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Henan Tuoren Medical Device Co., Ltd.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Which product codes does it file in?

  • CBITube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector)1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K152251Endobronchial TubeHenan Tuoren Medical Device Co., Ltd. · 2016

The one decision as Henan Tuoren Medical Device Co., Ltd. →