510(k) Report

FDA applicant

Zhejiang Yikang Medical Technology Co., Ltd.

Lishui, CN1 decision2026–20260 recalls

FDA records 1 decision for Zhejiang Yikang Medical Technology Co., Ltd. (Lishui, CN) in 2026: 1 510(k) clearance. All are in product code ITI (Wheelchair, Powered). 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, physical medicine panel, where it files most

How often FDA has decided Zhejiang Yikang Medical Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2026

2026 (partial year): 1
2026high 1 (2026)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2026.

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

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Which product codes does it file in?

  • ITIWheelchair, Powered1decision

What has FDA decided for it lately?

  • K253789Electric wheelchairZhejiang Yikang Medical Technology Co., Ltd. · 2026

The one decision as Zhejiang Yikang Medical Technology Co., Ltd. →