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Critical Device Corp.

United StatesFDA 510(k) applicant, unverified

Devices
6

What Critical Device Corp. makes

Critical Device Corp. manufactures needleless injection site adapters and related intravenous (IV) sets, including the NIMA Needleless InjectionSite Master Adapter with Posiflow positive displacement feature and standard versions, as well as MPS gravity flow control sets. The company also produces CDC vial and bag access pins (models P-1 through P-5) and macrobore tubing (models CDC-F-1 through CDC-F-11).

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

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue6

Newest first, rows 1-6 of 6

Frequently asked questions

How many devices does Critical Device Corp. have in the registry?

The registry currently lists 6 devices for Critical Device Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Critical Device Corp.'s devices?

Among its 6 most recently registered devices, Critical Device Corp. has devices listed in FDA 510(k) (6 devices).

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

Among its 6 most recently registered devices, the classes recorded for Critical Device Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Critical Device Corp. in the registry?

The most recently registered devices listed for Critical Device Corp. include NIMA NEEDLELESS INJECTIONSITE MASTER ADAPTER WITH POSIFLOW POSITIVE DISPLACEMENT FEATURE, AND I.V. SETS, NIMA NEEDLELESS INJECTIONSITE MASTER ADAPTER AND I.V. SET, MPS GRAVITY FLOW CONTROL SET and CDC VIAL AND BAG ACCESS PIN (CDC-P-1/P-2/P-3/P-4/P-5).

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