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J. Simmons Instrument, Ltd.

Country not established

Devices
1

What J. Simmons Instrument, Ltd. makes

J. Simmons Instrument, Ltd. manufactures the Needle Nabber, which is a medical device.

This product is classified as a Class II device and is listed in the FDA 510(k) registry. 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

  • The Needle Nabber Ref K911597

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does J. Simmons Instrument, Ltd. have in the registry?

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

Which registries list J. Simmons Instrument, Ltd.'s devices?

Among its 1 most recently registered device, J. Simmons Instrument, Ltd. has devices listed in FDA 510(k) (1 device).

What risk classes do J. Simmons Instrument, Ltd.'s devices fall under?

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

What are the newest devices from J. Simmons Instrument, Ltd. in the registry?

The most recently registered devices listed for J. Simmons Instrument, Ltd. include THE NEEDLE NABBER.

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