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Vxtra Corp.

United StatesFDA 510(k) applicant, unverified

Devices
10

What Vxtra Corp. makes

Vxtra Corp. manufactures single-use surgical instruments and kits for ophthalmic and microsurgical procedures, including disposable pre-gelled electrosurgical tools, irrigation/aspiration sets, and phacoemulsification kits. Their portfolio also includes ocutome tubing and blade systems for precision eye surgery, as well as adjustable and micro-sized surgical knives. Electrode systems for ECG monitoring are also part of their product line.

The company’s devices are regulated under FDA 510(k) clearance, spanning Class I and Class II classifications. Products are listed in the FDA’s 510(k) database, and the manufacturer operates from 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 Vxtra Corp. have in the registry?

The registry currently lists 10 devices for Vxtra Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Vxtra Corp.'s devices?

Among its 10 most recently registered devices, Vxtra Corp. has devices listed in FDA 510(k) (10 devices).

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

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

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

The most recently registered devices listed for Vxtra Corp. include OCUTOME PARATUBING SET, MICROSURGICAL BLADE, DISPOSABLE PRE-GELLED ELECTROSURGICAL and VXTRA BACK PACK EKG ELECTRODE CAT. NO..

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