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Artefactos DE Vidrio S.A. DE C.V.

MexicoFDA 510(k) applicant, unverified

Devices
1

Catalogue1

What Artefactos DE Vidrio S.A. DE C.V. makes

Artefactos DE Vidrio S.A. DE C.V. manufactures VEN-O-VAC blood collection vacuum tubes, designed for drawing and storing blood samples in clinical settings.

These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.

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

Frequently asked questions

How many devices does Artefactos DE Vidrio S.A. DE C.V. have in the registry?

The registry currently lists 1 device for Artefactos DE Vidrio S.A. DE C.V.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Artefactos DE Vidrio S.A. DE C.V.'s devices?

Among its 1 most recently registered device, Artefactos DE Vidrio S.A. DE C.V. has devices listed in FDA 510(k) (1 device).

What risk classes do Artefactos DE Vidrio S.A. DE C.V.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Artefactos DE Vidrio S.A. DE C.V.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Artefactos DE Vidrio S.A. DE C.V. in the registry?

The most recently registered devices listed for Artefactos DE Vidrio S.A. DE C.V. include VEN-O-VAC BLOOD COLLECTION VACUUM TUBES.

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