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Globe Ent., Inc.

United StatesFDA applicant, unverified

Devices
5

What Globe Ent., Inc. makes

Globe Ent., Inc. manufactures intravenous administration sets, including models with 15 and 60 drops per milliliter, as well as buret infusion sets in 100ml and 150ml sizes. The company also produces latex patient examination gloves and surgical gloves, alongside blood transfusion sets designed for medical use.

The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These items are listed in the FDA’s 510(k) clearance registry, and the manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

Frequently asked questions

How many devices does Globe Ent., Inc. have in the registry?

The registry currently lists 5 devices for Globe Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Globe Ent., Inc.'s devices?

Among its 5 most recently registered devices, Globe Ent., Inc. has devices listed in FDA 510(k) (5 devices).

What risk classes do Globe Ent., Inc.'s devices fall under?

Among its 5 most recently registered devices, the classes recorded for Globe Ent., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Globe Ent., Inc. in the registry?

The most recently registered devices listed for Globe Ent., Inc. include PROTOS I.V. ADMINISTRATION SET (15 DROPS/ML) I4070S/(60 DROPS/ML)I4670S PRELIMINARY, PATIENT EXAMINATION GLOVES (LATEX), SURGICAL GLOVES and PROTOS 100ML BURETTE INFUSION SET/ PROTOS 150ML BURETTE INFUSION SET.

Generated automatically from registry data and not verified by a human reviewer.