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Trillium Medical, Inc.

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Devices
1

What Trillium Medical, Inc. makes

Trillium Medical, Inc. manufactures the Micropulse Phacoemulsification System, a device used for cataract surgery to emulsify and remove the clouded lens through ultrasonic vibrations.

The Micropulse Phacoemulsification System is classified as a Class II medical device in the US and is listed under 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.

Catalogue1

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Frequently asked questions

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

The registry currently lists 1 device for Trillium Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Trillium Medical, Inc.'s devices?

Among its 1 most recently registered device, Trillium Medical, Inc. has devices listed in FDA 510(k) (1 device).

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

Among its 1 most recently registered device, the classes recorded for Trillium Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Trillium Medical, Inc. include MICROPULSE PHACOEMULSIFICATION SYSTEM.

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