FDA applicant
Wenzhou Bokang Instruments Co., Ltd.
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
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
2026 so far, outlined.
Recalls per year
No recall linked to its devices since 2012.
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.
See the 510(k) Report