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U. S. Surgical Corp.

United StatesFDA 510(k) applicant, unverified

Devices
2

What U. S. Surgical Corp. makes

U.S. Surgical Corp. manufactures automated suturing devices, including the AUTO SUTURE system, and disposable components for endoscopic linear staplers, such as the EEA Surgical Stapler.

Their portfolio includes Class I and Class II devices, all of which are listed via the FDA’s 510(k) pathway. The company is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

Frequently asked questions

How many devices does U. S. Surgical Corp. have in the registry?

The registry currently lists 2 devices for U. S. Surgical Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list U. S. Surgical Corp.'s devices?

Among its 2 most recently registered devices, U. S. Surgical Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do U. S. Surgical Corp.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for U. S. Surgical Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from U. S. Surgical Corp. in the registry?

The most recently registered devices listed for U. S. Surgical Corp. include AUTO SUTURE and AUTO SUTURE DISPOS., EEA SURG. STAPLER.

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