FDA applicant

Inmed Gloves Factory

Weifang, Shandong, CN1 decision2011–20110 recalls

FDA records 1 decision for Inmed Gloves Factory (Weifang, Shandong, CN) in 2011: 1 510(k) clearance. All are in product code LYZ (Vinyl Patient Examination Glove). 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 Inmed Gloves Factory’s devices, and how often a recall has named them.

FDA decisions per year

1in 2011

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

FIG. 1 — Inmed Gloves Factory by year, 2011–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Inmed Gloves Factory’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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Other applicant names beginning “Inmed”

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

Inmed Corp. 35

Inmed Gloves Factory

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Inmed”