510(k) Report

FDA applicant

Xuzhou Yongkang Electronic Science Technology Co., Ltd.

Xuzhou, CN6 decisions2017–20260 recalls

FDA records 6 decisions for Xuzhou Yongkang Electronic Science Technology Co., Ltd. (Xuzhou, CN) from 2017 to 2026: 6 510(k) clearances. Most are in product codes DXN (System, Measurement, Blood-Pressure…) and FTC (Light, Ultraviolet, Dermatological). Since 2016 its 510(k)s took a median of 228 days from receipt to decision, against 205 for FDA’s reviews in the same codes and years. Its devices cite 7 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 Xuzhou Yongkang Electronic Science Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2020

2017: 12018: 22019: 12020: 12026 (partial year): 1
2017high 2 (2018) · low 0 (2021)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Xuzhou Yongkang Electronic Science Technology Co., Ltd. by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Xuzhou”

FDA records each applicant name separately; these may or may not be the same firm.