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Newman Assoc.

Country not established

Devices
1

What Newman Assoc. makes

Newman Assoc. manufactures ON TARGET, a Class U medical device designed for targeted diagnostic or therapeutic procedures.

The device is regulated under the FDA’s 510(k) pathway and is listed in the U.S. regulatory database. The company is based in the United States.

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • On Target Ref K851887

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

Frequently asked questions

How many devices does Newman Assoc. have in the registry?

The registry currently lists 1 device for Newman Assoc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Newman Assoc.'s devices?

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

What are the newest devices from Newman Assoc. in the registry?

The most recently registered devices listed for Newman Assoc. include ON TARGET.

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