510(k) Report

FDA applicant

Luoyang Sunmed Devices Co., Ltd.

Luoyang, CN1 decision2022–20220 recalls

FDA records 1 decision for Luoyang Sunmed Devices Co., Ltd. (Luoyang, CN) in 2022: 1 510(k) clearance. All are in product code FXX (Mask, Surgical). 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, general and plastic surgery panel, where it files most

How often FDA has decided Luoyang Sunmed Devices Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2022

2022: 1
2022high 1 (2022) · low 0 (2023)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2022.

FIG. 1 — Luoyang Sunmed Devices Co., Ltd. by year, 2022–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Luoyang Sunmed Devices Co., Ltd.’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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Which product codes does it file in?

  • FXXMask, Surgical1decision

Whose devices does it build on?

Its devices cite 2 predicates; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K222335Surgical MaskLuoyang Sunmed Devices Co., Ltd. · 2022

The one decision as Luoyang Sunmed Devices Co., Ltd. →