FDA applicant

Medi-Globe Corp.

Tempe, AZ26 decisions1990–20260 recalls

FDA records 26 decisions for Medi-Globe Corp. (Tempe, AZ) from 1990 to 2026: 26 510(k) clearances. Most are in product codes FCG (Biopsy Needle) and FGE (Stents, Drains And Dilators For The Biliary…). Its devices cite 24 predicates, 11 of them its own earlier devices. No recall is linked to its devices.

FDA’s records also spell it “Medi-Globe Corporation”, “Medi-Globe GmbH”.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, gastroenterology and urology panel, where it files most

How often FDA has decided Medi-Globe Corp.’s devices, and how often a recall has named them.

FDA decisions per year

1in 2016

2007high 2 (2009) · low 0 (2008)2026

2026 so far, outlined.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medi-Globe 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-Globe”

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

Medi-Tech, Inc. 36 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-Source, Inc. 4

Medi-Globe Corp.

Which product codes does it file in?

Whose devices does it build on?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Medi-Globe”