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Coherent Medical Division

Country not established

Devices
7

What Coherent Medical Division makes

Coherent Medical Division manufactures surgical lasers, ophthalmic imaging and diagnostic devices, and laser accessories. Their portfolio includes CO₂ surgical lasers for precision tissue procedures, retinal cameras for fundus imaging, and laser systems for ophthalmic treatments like YAG capsulotomy. They also produce autorefractors for eye examinations and fundus cameras for retinal diagnostics.

The company’s devices are regulated under FDA pathways, including 510(k) clearances for Class I and II products and PMA submissions for Class III devices. Their portfolio appears in the FDA’s 510(k) and PMA registries, reflecting compliance with US medical device regulations. The manufacturer is based in the United States.

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

Catalogue7

Newest first, rows 1-7 of 7

Frequently asked questions

How many devices does Coherent Medical Division have in the registry?

The registry currently lists 7 devices for Coherent Medical Division. Devices recorded under merged duplicate company entries are counted once.

Which registries list Coherent Medical Division's devices?

Among its 7 most recently registered devices, Coherent Medical Division has devices listed in FDA 510(k) (6 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Coherent Medical Division's devices fall under?

Among its 7 most recently registered devices, the classes recorded for Coherent Medical Division's devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Coherent Medical Division in the registry?

The most recently registered devices listed for Coherent Medical Division include ACCESSORIES FOR SYS. 400 CO2 SURG. LASER, THE OCUPLOT D, MODEL 900K PHOTOCOAGULATOR and DIOPTRON III AUTOREFRACTOR.

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