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Phx Technologies Corp.

United StatesFDA applicant, unverified

Devices
49

What Phx Technologies Corp. makes

Phx Technologies Corp. manufactures single-use and reusable surgical instruments for minimally invasive procedures, including endoscopic tools like blunt-tipped trocar obturators, suction cannulas, and dissecting instruments. Their portfolio also includes specialized devices such as a sterile disposable endoscopic trumpet valve, bowel grasper tools, and a stone extractor for urological applications. Additional offerings include a retrograde knife, a malleable blunt dissector, and a watts rake with a Leur lock port for fluid management.

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

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

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Frequently asked questions

How many devices does Phx Technologies Corp. have in the registry?

The registry currently lists 49 devices for Phx Technologies Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Phx Technologies Corp.'s devices?

Among its 49 most recently registered devices, Phx Technologies Corp. has devices listed in FDA 510(k) (49 devices).

What risk classes do Phx Technologies Corp.'s devices fall under?

Among its 49 most recently registered devices, the classes recorded for Phx Technologies Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Phx Technologies Corp. in the registry?

The most recently registered devices listed for Phx Technologies Corp. include HYDRO-PROBE, STERILE, DISPOSABLE ENDOSCOPIC TRUMPET VALVE, WATTS RAKE WITH LEUR LOCK PORT and 5, 6, 7, 9, 10, 11&12MM BLUNT-TIPPED TROCAR OBTURATORS.

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