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Stik Stoppers, Inc.

Country not established

Devices
1

What Stik Stoppers, Inc. makes

Stik Stoppers, Inc. manufactures THE VAULT, a medical device designed to secure and immobilize intravenous (IV) lines, ports, or catheters to prevent accidental dislodgment or contamination during patient care.

THE VAULT is classified as a Class II device under FDA regulations and is listed via 510(k) clearance. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • The Vault Ref K990936

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

Frequently asked questions

How many devices does Stik Stoppers, Inc. have in the registry?

The registry currently lists 1 device for Stik Stoppers, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Stik Stoppers, Inc.'s devices?

Among its 1 most recently registered device, Stik Stoppers, Inc. has devices listed in FDA 510(k) (1 device).

What risk classes do Stik Stoppers, Inc.'s devices fall under?

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

What are the newest devices from Stik Stoppers, Inc. in the registry?

The most recently registered devices listed for Stik Stoppers, Inc. include THE VAULT.

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