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Neostar Medical Technologies, Inc.

United StatesFDA applicant, unverified

Devices
4

What Neostar Medical Technologies, Inc. makes

Neostar Medical Technologies, Inc. manufactures sterile medical trays and components for acute central venous access, including central venous access catheter trays, spreadable sheath introducer sets, and dual lumen catheter trays. These products are designed for short-term vascular access procedures in clinical settings.

The company’s portfolio is regulated under FDA Class II devices and requires 510(k) clearance for market authorisation. Products are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.

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

Catalogue4

Newest first, rows 1-4 of 4

Frequently asked questions

How many devices does Neostar Medical Technologies, Inc. have in the registry?

The registry currently lists 4 devices for Neostar Medical Technologies, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Neostar Medical Technologies, Inc.'s devices?

Among its 4 most recently registered devices, Neostar Medical Technologies, Inc. has devices listed in FDA 510(k) (4 devices).

What risk classes do Neostar Medical Technologies, Inc.'s devices fall under?

Among its 4 most recently registered devices, the classes recorded for Neostar Medical Technologies, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Neostar Medical Technologies, Inc. in the registry?

The most recently registered devices listed for Neostar Medical Technologies, Inc. include ACUTE CENTRAL VENOUS ACCESS CATHETER TRAY, ACUTE CENTRAL VENOUS ACCESS CATHETER (ACVAC), SPREADABLE SHEATH INTRODUCER SET and DUAL LUMEN CATHETER (DLC) TRAY.

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