Skip to content

Con Med Equipment, Inc.

United StatesFDA applicant, unverified

Devices
3

What Con Med Equipment, Inc. makes

Con Med Equipment, Inc. manufactures disposable and reusable medical devices for procedural and surgical use, including esophageal pill electrodes for cardiac mapping, dispersive electrosurgical ground pads for patient safety during surgery, and a pediatric ventilator (Venti-Gard Jr.) designed for neonatal and infant respiratory support.

The company’s products are regulated under FDA Class I and Class II classifications, with most devices requiring 510(k) clearance. These devices are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Esophageal Pill Electrode Ref K810895

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Electrosurgical Ground Pad-Dispersive Ref K830613

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Venti-Gard Jr. Ref K810896

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

Frequently asked questions

How many devices does Con Med Equipment, Inc. have in the registry?

The registry currently lists 3 devices for Con Med Equipment, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Con Med Equipment, Inc.'s devices?

Among its 3 most recently registered devices, Con Med Equipment, Inc. has devices listed in FDA 510(k) (3 devices).

What risk classes do Con Med Equipment, Inc.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for Con Med Equipment, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Con Med Equipment, Inc. in the registry?

The most recently registered devices listed for Con Med Equipment, Inc. include ESOPHAGEAL PILL ELECTRODE, ELECTROSURGICAL GROUND PAD-DISPERSIVE and VENTI-GARD JR..

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