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Durect Corp.

Country not established

Devices
1

What Durect Corp. makes

Durect Corp. manufactures microdose catheters, including models 90121-201, -202, and -203, designed for precise drug delivery applications.

These devices fall under FDA Class II regulation and are listed via 510(k) clearance. The company is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

Frequently asked questions

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

The registry currently lists 1 device for Durect Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Durect Corp.'s devices?

Among its 1 most recently registered device, Durect Corp. has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for Durect Corp.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Durect Corp. include MICRODOSE CATH, MODELS 90121-201, -202, -203.

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