FDA applicant

Globe Ent., Inc.

Houston, TX5 decisions1989–19970 recalls

FDA records 5 decisions for Globe Ent., Inc. (Houston, TX) from 1989 to 1997: 5 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and KGO (Surgeon'S Gloves). 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 Globe Ent., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Globe Ent., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Globe Ent., Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

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Other applicant names beginning “Globe”

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

Globe Management Support, Inc. 2 Globe Safety Products, Inc. 2 Globe Safety Equipment, Inc. 1

Globe Ent., Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Globe”