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Neward Enterprises, Inc.

United StatesFDA applicant, unverified

Devices
8

What Neward Enterprises, Inc. makes

Neward Enterprises, Inc. manufactures obstetrical vacuum delivery kits and disposable vacuum extractors for assisted childbirth, including single-use devices with directional and standard cup styles. Their portfolio also includes spiral electrodes for medical procedures and a venous access device called VENA * BRIDGE. Disposable leg plates for obstetric use are part of their product line.

The company’s devices are classified as Class II under FDA regulations and are supported by 510(k) clearances. Their 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.

Catalogue8

Newest first, rows 1-8 of 8

Frequently asked questions

How many devices does Neward Enterprises, Inc. have in the registry?

The registry currently lists 8 devices for Neward Enterprises, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Neward Enterprises, Inc.'s devices?

Among its 8 most recently registered devices, Neward Enterprises, Inc. has devices listed in FDA 510(k) (8 devices).

What risk classes do Neward Enterprises, Inc.'s devices fall under?

Among its 8 most recently registered devices, the classes recorded for Neward Enterprises, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Neward Enterprises, Inc. in the registry?

The most recently registered devices listed for Neward Enterprises, Inc. include MITYVAC(R) SAFTISOFT OBSTETRICAL VACUUM DELIV KIT, CR SPIRAL ELECTRODE, MITYVAC M STYLE VACUUM EXTRACTOR, DISPOSABLE and MITYVAC DIRECTIONAL VACUUM EXTRACTOR, DISPOSABLE.

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