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Clive Craig Co.

Country not established

Devices
2

What Clive Craig Co. makes

Clive Craig Co. manufactures the TRUJECT, a single-use, disposable injection device designed for subcutaneous or intramuscular administration of medications, and the PEEL-VUE autoclave/chemical pouch system, which provides sterilization and chemical processing for medical devices and supplies.

The company’s portfolio is regulated under FDA’s Class II device classification, with devices authorised via the 510(k) pathway. Their products are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Truject Ref K945284

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Peel-Vue Autoclave/Chemicalve Pouch Ref K894437

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

Frequently asked questions

How many devices does Clive Craig Co. have in the registry?

The registry currently lists 2 devices for Clive Craig Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Clive Craig Co.'s devices?

Among its 2 most recently registered devices, Clive Craig Co. has devices listed in FDA 510(k) (2 devices).

What risk classes do Clive Craig Co.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Clive Craig Co.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Clive Craig Co. in the registry?

The most recently registered devices listed for Clive Craig Co. include TRUJECT and PEEL-VUE AUTOCLAVE/CHEMICALVE POUCH.

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