Skip to content

Therex Corp.

United StatesFDA applicant, unverified

Devices
26

What Therex Corp. makes

Therex Corp. manufactures non-coring Huber needles and implantable vascular access systems, including low-profile titanium ports and detachable catheter systems. Products include port lines, catheters, and vascular access devices designed for long-term intravenous therapy and medication administration.

The company’s portfolio consists of Class II medical devices, all of which are listed under the FDA’s 510(k) clearance process. These devices are intended for use in the United States, where regulatory compliance is managed through the FDA’s regulatory framework.

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

Catalogue26

Newest first, rows 1-26 of 26

Search and filter all 26 devices
Skip device list

Rows 1-26 of 26

Frequently asked questions

How many devices does Therex Corp. have in the registry?

The registry currently lists 26 devices for Therex Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Therex Corp.'s devices?

Among its 26 most recently registered devices, Therex Corp. has devices listed in FDA 510(k) (26 devices).

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

Among its 26 most recently registered devices, the classes recorded for Therex Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Therex Corp. in the registry?

The most recently registered devices listed for Therex Corp. include NON-CORNING (HUBER) NEEDLE, A-PORT IMPLANT VASC ACCESS SYST LINE EXT-A2 PORT, THEREX LOW-PROFILE PORT 1.5MM I.D. X 2.7MM O.D. DETACHED CATHETER SYSTEM and LOW PROFILE TITANIUM MODEL CATALOG #1003.

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