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Norwich Eaton Pharmaceuticals, Inc.

United StatesFDA applicant, unverified

Devices
10

What Norwich Eaton Pharmaceuticals, Inc. makes

Norwich Eaton Pharmaceuticals, Inc. manufactures enteral feeding devices, including tungsten-tipped tubes for gastric and jejunostomy placements, such as twisted wire, wound, and braided designs. Their portfolio also covers complete enteral feeding systems and gastrostomy tubes designed for long-term nutritional support.

These devices are classified under FDA Class I and Class II regulations, with relevant submissions recorded in the FDA’s 510(k) clearance database. The company is based in the United States.

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

Catalogue10

Newest first, rows 1-10 of 10

Frequently asked questions

How many devices does Norwich Eaton Pharmaceuticals, Inc. have in the registry?

The registry currently lists 10 devices for Norwich Eaton Pharmaceuticals, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Norwich Eaton Pharmaceuticals, Inc.'s devices?

Among its 10 most recently registered devices, Norwich Eaton Pharmaceuticals, Inc. has devices listed in FDA 510(k) (10 devices).

What risk classes do Norwich Eaton Pharmaceuticals, Inc.'s devices fall under?

Among its 10 most recently registered devices, the classes recorded for Norwich Eaton Pharmaceuticals, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Norwich Eaton Pharmaceuticals, Inc. in the registry?

The most recently registered devices listed for Norwich Eaton Pharmaceuticals, Inc. include VIVONEX TUNGSTEN TIP TUBE-TWISTED WIRE, VIVONEX TUNGSTEN TIP TUBE-WOUND, VIVONEX ACUTROL ENTERNAL FEEDING SYS and VIVONEX MASS GASTRASTOMY TUBE.

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