510(k) Report

FDA applicant

Shenzhen Xft Medical Limited

Shenzhen, CN4 decisions2017–20210 recalls

FDA records 4 decisions for Shenzhen Xft Medical Limited (Shenzhen, CN) from 2017 to 2021: 4 510(k) clearances. Most are in product codes GZI (Stimulator, Neuromuscular, External Functional) and IPF (Stimulator, Muscle, Powered). Since 2016 its 510(k)s took a median of 137 days from receipt to decision, against 121 for FDA’s reviews in the same codes and years. Its devices cite 5 predicates, 1 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, neurology panel, where it files most

How often FDA has decided Shenzhen Xft Medical Limited’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2017: 12020: 22021: 1
2017high 2 (2020) · low 0 (2018)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2017.

FIG. 1 — Shenzhen Xft Medical Limited by year, 2017–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Shenzhen Xft Medical Limited’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