FDA applicant

Hong Kong Etech Groups Limited

Hong Kong, CN1 decision2024–20240 recalls

FDA records 1 decision for Hong Kong Etech Groups Limited (Hong Kong, CN) in 2024: 1 510(k) clearance. All are in product code NUH (Stimulator, Nerve, Transcutaneous…). Its devices cite 2 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, neurology panel, where it files most

How often FDA has decided Hong Kong Etech Groups Limited’s devices, and how often a recall has named them.

FDA decisions per year

1in 2024

2024high 1 (2024) · low 0 (2025)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2024.

FIG. 1 — Hong Kong Etech Groups Limited by year, 2024–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Hong Kong Etech Groups 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

Other applicant names beginning “Hong”

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

Hong Qiangxing (Shenzhen) Electronics Limited 10 Hong DI Plastic Products Co., Ltd. 5 Hong Seng Gloves Sdn Bhd 4 Hong Huang Tang Industrial Co., Ltd. 3 Hong YA Non-Woven Products Co., Ltd. 2 Hong Xin Rubber Products Co., Ltd. 1

Hong Kong Etech Groups Limited

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Hong”