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Tucker & Associates

Country not established

Devices
4

What Tucker & Associates makes

Tucker & Associates manufactures single-use barrier devices for medical procedures, including latex finger cots without powder and protein labeling for allergen reduction, as well as surgical face masks in multiple colors for visibility and procedural differentiation.

Their products are regulated under FDA Class I and Class II designations, with some devices subject to 510(k) clearance. The company’s devices are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.

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

Catalogue4

Newest first, rows 1-4 of 4

Frequently asked questions

How many devices does Tucker & Associates have in the registry?

The registry currently lists 4 devices for Tucker & Associates. Devices recorded under merged duplicate company entries are counted once.

Which registries list Tucker & Associates's devices?

Among its 4 most recently registered devices, Tucker & Associates has devices listed in FDA 510(k) (4 devices).

What risk classes do Tucker & Associates's devices fall under?

Among its 4 most recently registered devices, the classes recorded for Tucker & Associates's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Tucker & Associates in the registry?

The most recently registered devices listed for Tucker & Associates include FACE MASK, SURGICAL MASK, NON-STERILE, NITRILE EXAM GLOVE, POWDER-FREE, BLUE, LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING and SURGICAL FACE MASK - COLORS: WHITE, YELLOW, PINK, BLUE, AND GREEN.

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