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Nissho Corp.

United StatesFDA applicant, unverified

Devices
5

What Nissho Corp. makes

Nissho Corp. manufactures single-use medical devices for vascular access and hemodialysis, including arterial and venous catheters, disposable syringes and needles, blood tubing sets, fistula needles, and scalp vein infusion sets. Their products are designed for clinical use in dialysis procedures and intravenous therapies, ensuring compatibility with hemodialysis systems and patient safety in venous access applications.

The company’s portfolio is classified under FDA Class II devices, with each product authorised through the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) registry, adhering to US regulatory requirements for medical devices. The manufacturer operates from the United States.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

Frequently asked questions

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

The registry currently lists 5 devices for Nissho Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Nissho Corp.'s devices?

Among its 5 most recently registered devices, Nissho Corp. has devices listed in FDA 510(k) (5 devices).

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

Among its 5 most recently registered devices, the classes recorded for Nissho Corp.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Nissho Corp. include NIPRO SAFELET CATH, NIPRO BRANDED DISPOSABLE SYRINGES, NEEDLES, NIPRO ARTERIAL & VENOUS BLOOD TUBING SET FOR HEMODIALYSIS and NIPRO ARTERIAL VENOUS FISTULA NEEDLE.

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