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Normeca Corp.

NorwayFDA applicant, unverified

Devices
1

What Normeca Corp. makes

Normeca Corp. manufactures medical-grade rack systems and syringes designed for sterile drug preparation and administration, supporting hospital pharmacies and clinical settings.

The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. Normeca Corp. is based in the United States.

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

Catalogue1

Newest first, rows 1-1 of 1

  • Rack And Syringes Ref K915780

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

Frequently asked questions

How many devices does Normeca Corp. have in the registry?

The registry currently lists 1 device for Normeca Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Normeca Corp.'s devices?

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

What risk classes do Normeca Corp.'s devices fall under?

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

What are the newest devices from Normeca Corp. in the registry?

The most recently registered devices listed for Normeca Corp. include RACK AND SYRINGES.

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