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Conmed Andover Medical, Inc.

Also registered as Andover Medical, Inc.

United StatesFDA applicant, unverified

Devices
29

What Conmed Andover Medical, Inc. makes

Conmed Andover Medical, Inc. manufactures single-use and reusable ECG electrodes, including radiotranslucent monitoring electrodes for surgical environments, standard monitoring electrodes, and cloth electrodes for transcutaneous electrical nerve stimulation (TENS) and brain stimulation (BNES). Their product line also includes disposable surgical cables designed for temporary use in operating rooms.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.

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

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Frequently asked questions

How many devices does Conmed Andover Medical, Inc. have in the registry?

The registry currently lists 29 devices for Conmed Andover Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Conmed Andover Medical, Inc.'s devices?

Among its 29 most recently registered devices, Conmed Andover Medical, Inc. has devices listed in FDA 510(k) (29 devices).

What risk classes do Conmed Andover Medical, Inc.'s devices fall under?

Among its 29 most recently registered devices, the classes recorded for Conmed Andover Medical, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Conmed Andover Medical, Inc. in the registry?

The most recently registered devices listed for Conmed Andover Medical, Inc. include DIRECT CURRENT BONE GROWTH STIM. AN. PAD, CANMED 451, 2700 CLEARTRACE RADIOTRANSLUCENT MONITORING ECG ELECTROBE and MODIFIED LABEL CHANGE TO MODEL 5455 SURGICAL CABLE.

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