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Ximed/Prosure/Injectx

Country not established

Devices
9

What Ximed/Prosure/Injectx makes

The company manufactures electrosurgical probes and instruments, including bipolar and isolated saline-based variants, as well as gel-coated devices for surgical applications. It also produces injection and aspiration needles, such as the Tunis and TPI/TPI Flex series, alongside percutaneous injection/aspiration probes. Electrode and probe devices are designed for use in medical procedures requiring precise electrical conduction or fluid management.

These products are regulated under FDA 510(k) clearance, with devices classified as Class I or Class II. The portfolio is listed in the FDA’s 510(k) registry. The manufacturer operates from the United States.

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

Catalogue9

Newest first, rows 1-9 of 9

Frequently asked questions

How many devices does Ximed/Prosure/Injectx have in the registry?

The registry currently lists 9 devices for Ximed/Prosure/Injectx. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ximed/Prosure/Injectx's devices?

Among its 9 most recently registered devices, Ximed/Prosure/Injectx has devices listed in FDA 510(k) (9 devices).

What risk classes do Ximed/Prosure/Injectx's devices fall under?

Among its 9 most recently registered devices, the classes recorded for Ximed/Prosure/Injectx's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Ximed/Prosure/Injectx in the registry?

The most recently registered devices listed for Ximed/Prosure/Injectx include ELECTRODES/PROBES/DEVICES, ISOLATED SALINE ELECTRODES/PROBES/DEVICES-SALINETRODE, BIPOLAR ELECTROSURGICAL PROBES AND INSTRUMENTS and ELECTROSURGICAL PROBES AND DEVICES-GELTX.

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