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Lasermatic, Inc.

Also registered as Lasermatic OY

Country not established

Devices
10

What Lasermatic, Inc. makes

Lasermatic, Inc. manufactures surgical laser systems, including the Model 5050 SurgiLaser for neurosurgery, gastro-intestinal, urology, OB-GYN, and pulmonary procedures, as well as the Combolaser Model 5050 and the Lasermatic SuperCombo™ Surgical Laser System.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue10

Newest first, rows 1-10 of 10

Frequently asked questions

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

The registry currently lists 10 devices for Lasermatic, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Lasermatic, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Lasermatic, Inc. include MODEL 5050 SURGILASER FOR NEUROSURGERY USE, MODEL 5050 SURGILASER FOR GASTRO-INTESTINAL USE, MODIFIED COMBOLASER 5050 & NEW MODEL 5050 VER. 33 and MODEL 5050 SURGILASER FOR UROLOGY USE.

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