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Plastic Injectors, Inc.

United StatesFDA applicant, unverified

Devices
8

What Plastic Injectors, Inc. makes

Plastic Injectors, Inc. manufactures disposable microtitration plates and inoculum trays for laboratory use, including the CODE-A-WELL Series 200, 300, and 350 plates, as well as microtitration strips and high-capacity variants like the Series 1-600 and 1-1000. The company also produces the OPTI-POINT, a specialized device for precise liquid handling in research and diagnostic settings. These products are designed for use in serological, microbiological, and biochemical assays.

The portfolio includes devices classified as Class I and Class II under FDA regulations, with submissions supported by 510(k) clearance pathways. These products are listed in the FDA’s 510(k) database, reflecting their regulatory authorization for commercial distribution in the United States. The manufacturer is based in the US.

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

Catalogue8

Newest first, rows 1-8 of 8

Frequently asked questions

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

The registry currently lists 8 devices for Plastic Injectors, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Plastic Injectors, Inc.'s devices?

Among its 8 most recently registered devices, Plastic Injectors, Inc. has devices listed in FDA 510(k) (8 devices).

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

Among its 8 most recently registered devices, the classes recorded for Plastic Injectors, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Plastic Injectors, Inc. include CODE-A-WELL SERIES 200 PLATE, CODE-A-WALL SERIES 1-250 INOCULUM TRAY, CODE-A-WELL SERIES 300 PLATE and CODE-A-WELL SERIES 1-600, 1-625.

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