FDA applicant

Cathay Manufacturing Corp.

Shanghai, CN2 decisions2013–20160 recalls

FDA records 2 decisions for Cathay Manufacturing Corp. (Shanghai, CN) from 2013 to 2016: 2 510(k) clearances. Most are in product codes GEI (Electrosurgical, Cutting & Coagulation &…) and GXY (Electrode, Cutaneous). Its devices cite 3 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, general and plastic surgery panel, where it files most

How often FDA has decided Cathay Manufacturing Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2013high 1 (2013) · low 0 (2014)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2013.

FIG. 1 — Cathay Manufacturing Corp. by year, 2013–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Cathay Manufacturing Corp.’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 “Cathay”

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

Cathay Consolidated, Inc. 2 Cathay Health Care Equipment Manufacturing, Inc. 1 Cathay Manfacturing Corp. 1 Cathay International, Ltd. 1

Cathay Manufacturing Corp.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Cathay”