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Xanmed Corp.

United StatesFDA applicant, unverified

Devices
9

What Xanmed Corp. makes

Xanmed Corp. manufactures custom surgical kits and systems for specific medical procedures, including orthopedic, emergency room, cardiovascular, obstetrical/gynecological, and neurological applications. Their offerings include catheter introducer systems, subclavian lead introducer systems, and specialized surgical eye packs. These products are designed for use in minor office procedures, general surgery, and specialized surgical settings.

The company’s portfolio includes devices classified as Class I and Class II under FDA regulations, with several products listed via the 510(k) pathway. These devices are intended for use in the United States, where regulatory compliance is required for market authorization.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue9

Newest first, rows 1-9 of 9

Frequently asked questions

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

The registry currently lists 9 devices for Xanmed Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Xanmed Corp.'s devices?

Among its 9 most recently registered devices, Xanmed Corp. has devices listed in FDA 510(k) (9 devices).

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

Among its 9 most recently registered devices, the classes recorded for Xanmed Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Xanmed Corp. include ORTHOPEDIC CUSTOM SURGICAL KIT, EMERGENCY ROOM & MINOR OFFICE PROCEDURE CUSTOM KIT, CATHETER INTRODUCER SYSTEM and MISCELLANEOUS GENERAL SURGICAL CUSTOM KIT.

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