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Colin Corp.

JapanFDA applicant, unverified

Devices
1

What Colin Corp. makes

Colin Corp. manufactures the VP-2000/1000, a medical device designed for vascular procedures, including peripheral and coronary interventions.

The VP-2000/1000 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Vp-2000/1000 Ref K013434

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

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

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

Which registries list Colin Corp.'s devices?

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

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

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

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

The most recently registered devices listed for Colin Corp. include VP-2000/1000.

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