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Toys House Industrial Corp.

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Devices
1

What Toys House Industrial Corp. makes

Toys House Industrial Corp. manufactures the PULSATOR 5000, a medical device designed for respiratory therapy, likely used in neonatal or pediatric ventilation support.

The PULSATOR 5000 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. 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

  • Pulsator 5000 Ref K930102

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

Frequently asked questions

How many devices does Toys House Industrial Corp. have in the registry?

The registry currently lists 1 device for Toys House Industrial Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Toys House Industrial Corp.'s devices?

Among its 1 most recently registered device, Toys House Industrial Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Toys House Industrial Corp.'s devices fall under?

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

What are the newest devices from Toys House Industrial Corp. in the registry?

The most recently registered devices listed for Toys House Industrial Corp. include PULSATOR 5000.

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