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Kent Design & Manufacturing, Inc.

United StatesFDA applicant, unverified

Devices
6

What Kent Design & Manufacturing, Inc. makes

Kent Design & Manufacturing, Inc. produces portable isokinetic rehabilitation devices for targeted joint assessment and strengthening, including units for the back/abdomen, knee, shoulder, wrist/ankle, and hip. These systems are designed for clinical use in physical therapy and sports medicine settings to measure and improve muscle performance and joint function.

The company’s devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The portfolio is registered in the FDA’s 510(k) Premarket Notification database. The manufacturer is based in the United States.

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

Catalogue6

Newest first, rows 1-6 of 6

Frequently asked questions

How many devices does Kent Design & Manufacturing, Inc. have in the registry?

The registry currently lists 6 devices for Kent Design & Manufacturing, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kent Design & Manufacturing, Inc.'s devices?

Among its 6 most recently registered devices, Kent Design & Manufacturing, Inc. has devices listed in FDA 510(k) (6 devices).

What risk classes do Kent Design & Manufacturing, Inc.'s devices fall under?

Among its 6 most recently registered devices, the classes recorded for Kent Design & Manufacturing, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Kent Design & Manufacturing, Inc. in the registry?

The most recently registered devices listed for Kent Design & Manufacturing, Inc. include PORTABLE ISOKINETICS 3007 BACK/ABDOMEN UNIT, PORTABLE ISOKINETICS 3002 ISO KANE II, PORTABLE ISOKINETICS 3004 KNEE UNIT and PORTABLE ISOKINETICS 3003 SHOULDER UNIT.

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