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Cilco, Inc.

United StatesFDA 510(k) applicant, unverified

Devices
13

What Cilco, Inc. makes

Cilco, Inc. manufactures ophthalmic surgical instruments and equipment, including cystotomes, diamond knives, IOL forceps, and irrigation/aspiration handpieces. Their product portfolio also features ophthalmic endoscopes, surgical packs, A-scan and B-scan digital diagnostic systems, and the Octopus 500/500E visual field analyzer, alongside the K-Sol ophthalmic solution.

The company is based in the United States, and its devices are categorized under Class I, Class II, Class III, and U regulatory classifications. These products are listed in the FDA 510(k) and PMA regulatory databases.

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

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Frequently asked questions

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

The registry currently lists 13 devices for Cilco, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Cilco, Inc.'s devices?

Among its 13 most recently registered devices, Cilco, Inc. has devices listed in FDA 510(k) (12 devices) and FDA PMA (1 device). A device can be listed in more than one registry, so these counts overlap.

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

Among its 13 most recently registered devices, the classes recorded for Cilco, Inc.'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 Cilco, Inc. in the registry?

The most recently registered devices listed for Cilco, Inc. include CYSTOTOME, 140-S, CILCO I/A SURGICAL PACK, CILCOR OPHTHALMIC INSTRUMENTS and CILCO ASCAN.

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