510(k) Report

FDA applicant

Foshan Dahao Medical Technology Co., Ltd.

Foshan, CN4 decisions2022–20260 recalls

FDA records 4 decisions for Foshan Dahao Medical Technology Co., Ltd. (Foshan, CN) from 2022 to 2026: 4 510(k) clearances. All are in product code ITI (Wheelchair, Powered). Since 2016 its 510(k)s took a median of 142 days from receipt to decision, against 102 for FDA’s reviews in the same codes and years. Its devices cite 4 predicates, 0 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Foshan Dahao Medical Technology Co., Ltd.”.

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 Foshan Dahao Medical Technology Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2025

2022: 12025: 12026 (partial year): 2
2022high 2 (2026) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Foshan Dahao Medical Technology Co., Ltd. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Foshan Dahao Medical Technology Co.…’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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