Skip to content

Conmedcorp

Country not established

Devices
92

What Conmedcorp makes

The company manufactures single-use medical devices for surgical and monitoring applications, including malleable handpieces for orthopedic procedures, ECG electrodes for patient monitoring, insufflation tubing sets with filters, bipolar cords, and disposable electrosurgical grounding pads. It also produces intravenous dressings, irrigation nozzles, defibrillation/pacing pads, and systems for nasogastric or orogastric tube placement. Additional products include smoke evacuation attachments for surgical smoke management and pre-gelled disposable electrosurgical grounding electrodes.

The portfolio consists of devices classified as Class I, Class II, and Unclassified (U) under FDA regulations, with most products authorised via the 510(k) pathway. These devices are listed in the FDA’s 510(k) database. The company is headquartered in the United States.

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

Catalogue92

Newest first, rows 1-50 of 92

Search and filter all 92 devices
Skip device list

Rows 1-50 of 92

Showing 1-50 of 92

Frequently asked questions

How many devices does Conmedcorp have in the registry?

The registry currently lists 92 devices for Conmedcorp. Devices recorded under merged duplicate company entries are counted once.

Which registries list Conmedcorp's devices?

Among its 50 most recently registered devices, Conmedcorp has devices listed in FDA 510(k) (50 devices).

What risk classes do Conmedcorp's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Conmedcorp's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Conmedcorp in the registry?

The most recently registered devices listed for Conmedcorp include ECG ELECTRODE (VARIOUS), THERMOGARD & THERMOGARD PLUS ABC, CONMED UNIVERSAL PLUS and ELECTROSURGICAL DISPERSIVE ELECTRODE.

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