Skip to content

American Medical Optics

Country not established

Devices
17

What American Medical Optics makes

American Medical Optics manufactures ophthalmic surgical instruments and laser systems, including argon and krypton laser photocoagulators for retinal treatments, phacoemulsification kits for cataract surgery, and direct ophthalmoscopes for eye examinations. The company also produces intraocular lens guides and photokeratometry devices used in refractive surgery and corneal mapping. Irrigation kits and imaging systems for ocular procedures are part of its portfolio.

The company’s devices are classified under FDA categories Class I, Class II, and Class III, with many authorised via the 510(k) pathway. Products are listed in the FDA’s 510(k) registry. The manufacturer is based in the United States.

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

Catalogue17

Newest first, rows 1-17 of 17

Search and filter all 17 devices
Skip device list

Rows 1-17 of 17

Frequently asked questions

How many devices does American Medical Optics have in the registry?

The registry currently lists 17 devices for American Medical Optics. Devices recorded under merged duplicate company entries are counted once.

Which registries list American Medical Optics's devices?

Among its 17 most recently registered devices, American Medical Optics has devices listed in FDA 510(k) (17 devices).

What risk classes do American Medical Optics's devices fall under?

Among its 17 most recently registered devices, the classes recorded for American Medical Optics'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 American Medical Optics in the registry?

The most recently registered devices listed for American Medical Optics include AMERICAN MEDICAL OPTICS I/A KIT- IRRIG, AMERICAN MEDICAL OPTICS IMAGING SYS, AMER. MEDICAL OPTIC MONOCULAR DIRECT OPHTHALMASCOP and AMER. MEDICAL OPTICS ARGON/KRYPTON LASE.

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