Skip to content

Vermed, Inc.

Country not established

Devices
1
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Vermed, Inc. makes

Vermed, Inc. makes medical devices such as ECG electrodes, including prewired pediatric electrodes. These products are used for electrocardiography, a test that measures the electrical activity of the heart.

The company's portfolio is regulated as Class II devices and is listed in the FDA 510(k) registry. Vermed, Inc. is based in the US.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

FDA recall records list 1 recall initiated by Vermed, Inc., initiated on 2011-02-08. By recorded status: 1 terminated. The reasons filed fall into these groups: sterility or contamination. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2011

    • 8 Feb 2011 Z-2136-2011 Unclassified (pre-2012) Terminated Vermed kits contain a product component (Triad Alcohol Prep Pads) recalled due to potential Bacillus cereus contamination. Distribution: OR

Frequently asked questions

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

The registry currently lists 1 device for Vermed, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Vermed, Inc.'s devices?

Among its 1 most recently registered device, Vermed, Inc. has devices listed in FDA 510(k) (1 device).

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

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

Are there FDA recall records for Vermed, Inc.?

FDA recall records list 1 recall initiated by Vermed, Inc., the most recent initiated on 8 Feb 2011. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

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

The most recently registered devices listed for Vermed, Inc. include TENDER-TRODE PREWIRED PEDIATRIC ECG ELECTRODE.

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