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Taylor Industries, Inc.

Country not established FDA establishment FEI 1000520174

Devices
2
Registrations
FDA
FDA recalls
0

What Taylor Industries, Inc. makes

Taylor Industries, Inc. manufactures long-term monitoring electrodes and general-purpose monitoring electrodes.

These devices are classified as Class II medical devices and are listed in the FDA 510(k) registry. The company is based in the United States.

AI-generated from registry data, 5 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

Company details

FDA FEI number
1000520174
Address
2704 Industrial Dr, JEFFERSON CITY, MO, 65109

Frequently asked questions

How many devices does TAYLOR INDUSTRIES, INC. have in the registry?

The registry currently lists 2 devices for TAYLOR INDUSTRIES, INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list TAYLOR INDUSTRIES, INC.'s devices?

Among its 2 most recently registered devices, TAYLOR INDUSTRIES, INC. has devices listed in FDA 510(k) (2 devices).

What risk classes do TAYLOR INDUSTRIES, INC.'s devices fall under?

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

What are the newest devices from TAYLOR INDUSTRIES, INC. in the registry?

The most recently registered devices listed for TAYLOR INDUSTRIES, INC. include TAYLOR LONG TERM MONITORING ELECTRODE and TAYLOR GENERAL PURPOSE MONITORING ELECTRODE.

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

This is an FDA establishment record. No EUDAMED registration is known for this company and no recalls are recorded.