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Vanguard Container Corp.

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Devices
1

What Vanguard Container Corp. makes

Vanguard Container Corp. manufactures sterile, single-use medical containers designed for the containment and transport of pharmaceuticals, biologics, and other sensitive medical substances. These containers are engineered to maintain product integrity under controlled temperature and pressure conditions, ensuring compliance with sterile processing requirements in healthcare and research settings.

The company’s products fall under FDA Class II medical devices, requiring premarket notification (510(k)) clearance. These devices are listed in the FDA’s 510(k) database, adhering to U.S. regulatory standards for medical containers. The manufacturer operates from the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Vanguard Ref K946084

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Vanguard Container Corp. have in the registry?

The registry currently lists 1 device for Vanguard Container Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Vanguard Container Corp.'s devices?

Among its 1 most recently registered device, Vanguard Container Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Vanguard Container Corp.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Vanguard Container Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Vanguard Container Corp. in the registry?

The most recently registered devices listed for Vanguard Container Corp. include VANGUARD.

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