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Aerosport, Inc.

Country not established

Devices
1

What Aerosport, Inc. makes

Aerosport, Inc. manufactures the TEEN 100, a medical device designed for respiratory support or monitoring in pediatric patients.

The TEEN 100 is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Teen 100 Ref K945213

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

Frequently asked questions

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

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

Which registries list Aerosport, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Aerosport, Inc. include TEEN 100.

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