FDA applicant

Practical Protective Plastic Manufactory, Ltd.

Los Angeles, CA1 decision2006–20060 recalls

FDA records 1 decision for Practical Protective Plastic Manufactory, Ltd. (Los Angeles, CA) in 2006: 1 510(k) clearance. All are in product code LYZ (Vinyl Patient Examination Glove). 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 hospital panel, where it files most

How often FDA has decided Practical Protective Plastic Manufactory, Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Practical Protective Plastic Manufactory, Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Practical Protective Plastic Manufactory, Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Practical”

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

Practical Healthcare Devices, Inc. 1 Practical Navigation, LLC 1

Practical Protective Plastic Manufactory, 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 “Practical”