FDA applicant

Inner Mongolia Cureguard Medical Materials Co., Ltd.

Ulanqab, CN1 decision2021–20210 recalls

FDA records 1 decision for Inner Mongolia Cureguard Medical Materials Co., Ltd. (Ulanqab, CN) in 2021: 1 510(k) clearance. All are in product code LYZ (Vinyl Patient Examination Glove). Its devices cite 1 predicate, 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 hospital panel, where it files most

How often FDA has decided Inner Mongolia Cureguard Medical Materials Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2021

2021high 1 (2021) · low 0 (2022)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2021.

FIG. 1 — Inner Mongolia Cureguard Medical Materials Co., Ltd. by year, 2021–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Inner Mongolia Cureguard Medical…’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 “Inner”

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

Inner Mongolia Cureguard Medical Technology Co., Ltd. 3 Inner Mongolia Boming Medical Supplies Co., Ltd. 2 Inner Vision Biometrics Pty, Ltd. 1 Inner Act, LLC 1 Inner Vision Mri, Ltd. 1

Inner Mongolia Cureguard Medical Materials Co., Ltd.

Which product codes does it file in?

Whose devices does it build on?

What has FDA decided for it lately?

Other applicant names beginning “Inner”