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Posey Co.

Country not established

Devices
2

What Posey Co. makes

Posey Co. manufactures the POSEY CUFFLATOR and QUICKTRACH, which are medical devices intended for clinical use.

Both devices are classified as Class II and are listed in the FDA 510(k) registry. Posey Co. is based in the United States.

AI-generated from registry data, 24 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Posey Cufflator Ref K912723

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Quicktrach Ref K874742

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

Frequently asked questions

How many devices does Posey Co. have in the registry?

The registry currently lists 2 devices for Posey Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Posey Co.'s devices?

Among its 2 most recently registered devices, Posey Co. has devices listed in FDA 510(k) (2 devices).

What risk classes do Posey Co.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Posey Co.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Posey Co. in the registry?

The most recently registered devices listed for Posey Co. include POSEY CUFFLATOR and QUICKTRACH.

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