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Body Bike, Inc.

Country not established

Devices
1

What Body Bike, Inc. makes

Body Bike, Inc. manufactures the QUADTRAX, a medical device designed for therapeutic exercise and rehabilitation, incorporating a stationary bike with integrated resistance and motion tracking technology to support physical therapy and functional recovery.

The QUADTRAX is classified as a Class II device under FDA regulations and is authorised through the 510(k) clearance pathway. The company is headquartered in 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

  • Quadtrax Ref K935201

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

Frequently asked questions

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

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

Which registries list Body Bike, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Body Bike, Inc. include QUADTRAX.

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