510(k) Report

FDA applicant

Wenzhou Bokang Instruments Co., Ltd.

Wenzhou, CN2 decisions2012–20180 recalls

FDA records 2 decisions for Wenzhou Bokang Instruments Co., Ltd. (Wenzhou, CN) from 2012 to 2018: 2 510(k) clearances. Most are in product codes DXQ (Blood Pressure Cuff) and DXN (System, Measurement, Blood-Pressure…). 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 Wenzhou Bokang Instruments Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2018

2012: 12018: 1
2012high 1 (2012) · low 0 (2013)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2012.

FIG. 1 — Wenzhou Bokang Instruments Co., Ltd. by year, 2012–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Wenzhou Bokang Instruments 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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