FDA applicant

Medi Pure Corp.

Darul Ridzuan, Malaysia, MG1 decision1994–19940 recalls

FDA records 1 decision for Medi Pure Corp. (Darul Ridzuan, Malaysia, MG) in 1994: 1 510(k) clearance. All are in product code LYY (Latex 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 Medi Pure Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medi Pure Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Medi Pure Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Medi Pure Corp.’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 “Medi”

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

Medi-Tech, Inc. 36 Medi-Globe Corp. 26 Medi-Flex Hospital Products, Inc. 13 Medi-Plast Intl., Inc. 12 The Medi-Dose Group 10 Medi Nuclear Corp., Inc. 9 Medi-Physics Inc. Dba Nycomed Amersham Imaging 9 Medi-Craft, Ltd. 9 Medi-Spec 8 Medi-Man Rehabilitation Products, Inc. 4 Medi Tex, Inc. 4 Medi-Dose, Inc. 4

Medi Pure Corp.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Medi”