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Coll Partners, Ltd.

IsraelFDA applicant, unverified

Devices
1

What Coll Partners, Ltd. makes

Coll Partners, Ltd. manufactures the Proxivent Kit, a medical device designed for respiratory support and ventilation management in clinical settings.

The Proxivent Kit 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

  • The Proxivent Kit Ref K073061

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

Frequently asked questions

How many devices does Coll Partners, Ltd. have in the registry?

The registry currently lists 1 device for Coll Partners, Ltd.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Coll Partners, Ltd.'s devices?

Among its 1 most recently registered device, Coll Partners, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do Coll Partners, Ltd.'s devices fall under?

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

What are the newest devices from Coll Partners, Ltd. in the registry?

The most recently registered devices listed for Coll Partners, Ltd. include THE PROXIVENT KIT.

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