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Venisect, Inc.

Country not established

Devices
1

What Venisect, Inc. makes

Venisect, Inc. manufactures the Venisect Laser Lancet. This device is a laser-based instrument designed for blood sampling.

The product is classified as a Class II medical device and is listed in the FDA 510(k) database. The company is based in the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Venisect Laser Lancet Ref K955653

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

Frequently asked questions

How many devices does Venisect, Inc. have in the registry?

The registry currently lists 1 device for Venisect, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Venisect, Inc.'s devices?

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

What risk classes do Venisect, Inc.'s devices fall under?

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

What are the newest devices from Venisect, Inc. in the registry?

The most recently registered devices listed for Venisect, Inc. include VENISECT LASER LANCET.

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