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Needlepoint Guard, Inc.

United StatesFDA applicant, unverified

Devices
2

What Needlepoint Guard, Inc. makes

Needlepoint Guard, Inc. manufactures the Needlepoint Guard, a device designed to prevent needle stick injuries during medical procedures by providing a protective barrier around needles.

The company’s portfolio is regulated under FDA’s Class II device classification and is listed via the 510(k) pathway. The devices are based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Needlepoint Guard Ref K901546

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Needlepoint Guard Ref K895831

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

Frequently asked questions

How many devices does Needlepoint Guard, Inc. have in the registry?

The registry currently lists 2 devices for Needlepoint Guard, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Needlepoint Guard, Inc.'s devices?

Among its 2 most recently registered devices, Needlepoint Guard, Inc. has devices listed in FDA 510(k) (2 devices).

What risk classes do Needlepoint Guard, Inc.'s devices fall under?

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

What are the newest devices from Needlepoint Guard, Inc. in the registry?

The most recently registered devices listed for Needlepoint Guard, Inc. include NEEDLEPOINT GUARD.

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