Skip to content

Amerimed US Corp.

United StatesFDA applicant, unverified

Devices
5

What Amerimed US Corp. makes

Amerimed US Corp. manufactures latex and vinyl patient examination gloves, as well as ultrasonic surgical aspiration kits.

The company is based in the United States, and its portfolio includes devices classified as Class I and Class U that are listed in the FDA 510(k) registry.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue5

Newest first, rows 1-5 of 5

Frequently asked questions

How many devices does Amerimed US Corp. have in the registry?

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

Which registries list Amerimed US Corp.'s devices?

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

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

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

What are the newest devices from Amerimed US Corp. in the registry?

The most recently registered devices listed for Amerimed US Corp. include LATEX EXAM GLOVES (MFG. SHANGHAI MEHECO), PATIENT EXAMINATION GLOVES (LATEX), VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX) and AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT.

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