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Medoc Ltd. Advanced Medical Systems

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Devices
4

What Medoc Ltd. Advanced Medical Systems makes

Medoc Ltd. Advanced Medical Systems produces devices for neurological and sensory testing, including contact-heat evoked potential stimulators (CHEPS) and the Genito Sensory Analyzer (GSA). These tools are designed to assess pain thresholds, thermal sensitivity, and nerve function through controlled thermal stimulation and evoked potential measurement. The PATHWAY system integrates both ATS (automated temperature sensor) and CHEPS functionalities for combined testing.

The company’s devices are classified under FDA regulations as Class I and Class II, with some models requiring 510(k) clearance. They are listed in the FDA’s 510(k) database, indicating their regulatory status in the United States. The manufacturer operates from the US.

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

Catalogue4

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Frequently asked questions

How many devices does Medoc Ltd. Advanced Medical Systems have in the registry?

The registry currently lists 4 devices for Medoc Ltd. Advanced Medical Systems. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medoc Ltd. Advanced Medical Systems's devices?

Among its 4 most recently registered devices, Medoc Ltd. Advanced Medical Systems has devices listed in FDA 510(k) (4 devices).

What risk classes do Medoc Ltd. Advanced Medical Systems's devices fall under?

Among its 4 most recently registered devices, the classes recorded for Medoc Ltd. Advanced Medical Systems's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Medoc Ltd. Advanced Medical Systems in the registry?

The most recently registered devices listed for Medoc Ltd. Advanced Medical Systems include MODIFIED CONTACT-HEAT EVOKED POTENTIAL STIMULATOR (CHEPS), GSA GENITO SENSORY ANALYZER, PATHWAY - ATS/CHEPS and CONTACT HEAT-EVOKED POTENTIAL STIMULATOR (CHEPS).

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