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Greiner America, Inc.

United StatesFDA applicant, unverified

Devices
7

What Greiner America, Inc. makes

Greiner America, Inc. manufactures blood collection tubes, including variants with EDTA K3 anticoagulant, lithium heparin with gel separator, and clot activator with gel separator. These tubes are designed for venipuncture and serum/plasma separation in clinical laboratory settings.

The company’s products fall under FDA Class II devices and are authorised via the 510(k) pathway. They are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.

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

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

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

The registry currently lists 7 devices for Greiner America, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Greiner America, Inc.'s devices?

Among its 7 most recently registered devices, Greiner America, Inc. has devices listed in FDA 510(k) (7 devices).

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

Among its 7 most recently registered devices, the classes recorded for Greiner America, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Greiner America, Inc. include GREINER VACUETTE BLOOD COLLECTION TUBE, GREINER VACUETTE BLOOD COLLECTION TUBE E/EDTA K3, GREINER VACUETTE BLOOD COLLECTION TUBE W/LITHIUM HEPARIN & GEL SEPARATOR and GREINER VACUTTE BLOOD COLLECTION TUBE W/ CLOT ACTIVATOR & GEL SEPARATOR.

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