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Lysonix, Inc.

United StatesFDA applicant, unverified

Devices
5

What Lysonix, Inc. makes

Lysonix, Inc. manufactures devices for lipoplasty procedures, including access ports, suction systems, aspiration pumps, irrigation systems, and cannulas designed for tissue removal and fluid management during cosmetic surgery.

The company’s portfolio includes Class I and Class II devices, with products authorised via the FDA’s 510(k) pathway. These devices are listed under regulatory registries for surgical and aesthetic applications, and the company is based in the United States.

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

Catalogue5

Newest first, rows 1-5 of 5

Frequently asked questions

How many devices does Lysonix, Inc. have in the registry?

The registry currently lists 5 devices for Lysonix, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lysonix, Inc.'s devices?

Among its 5 most recently registered devices, Lysonix, Inc. has devices listed in FDA 510(k) (5 devices).

What risk classes do Lysonix, Inc.'s devices fall under?

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

What are the newest devices from Lysonix, Inc. in the registry?

The most recently registered devices listed for Lysonix, Inc. include LYSONIX LIPOPLASTY ACCESS PORT, LYSONIX SUCTION LIPOPLASTY SYSTEM, LYSONIX ASPIRATION PUMP and LYSONIX IRRIGATION SYSTEM.

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