FDA applicant

Medexel Medical Mfg. Co., Ltd.

Deer Field, IL1 decision2005–20050 recalls

FDA records 1 decision for Medexel Medical Mfg. Co., Ltd. (Deer Field, IL) in 2005: 1 510(k) clearance. All are in product code MEG (Syringe, Antistick). 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 Medexel Medical Mfg. Co., Ltd.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medexel Medical Mfg. Co., Ltd. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medexel Medical Mfg. Co., Ltd. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medexel Medical Mfg. Co., Ltd.’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 “Medexel”

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

Medexel Co.,Ltd 3

Medexel Medical Mfg. 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 “Medexel”