FDA applicant

Inpro Technology Device Factory

Weifang, Shandong, CN2 decisions2011–20160 recalls

FDA records 2 decisions for Inpro Technology Device Factory (Weifang, Shandong, CN) from 2011 to 2016: 2 510(k) clearances. 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 Inpro Technology Device Factory’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2011high 1 (2011) · low 0 (2012)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2011.

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

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Inpro Technology Device Factory

Which product codes does it file in?

What has FDA decided for it lately?