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Douglas C. Mckee & Co.

Country not established

Devices
1

What Douglas C. Mckee & Co. makes

Douglas C. Mckee & Co. manufactures an eyelid speculum, a handheld device used in ophthalmology to hold the eyelids open during eye examinations or procedures.

The eyelid speculum is classified as a Class I 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

Newest first, rows 1-1 of 1

  • Eyelid Speculum Ref K830430

    Class I
    Active 510(k) 510(k) I

Frequently asked questions

How many devices does Douglas C. Mckee & Co. have in the registry?

The registry currently lists 1 device for Douglas C. Mckee & Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Douglas C. Mckee & Co.'s devices?

Among its 1 most recently registered device, Douglas C. Mckee & Co. has devices listed in FDA 510(k) (1 device).

What risk classes do Douglas C. Mckee & Co.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Douglas C. Mckee & Co.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Douglas C. Mckee & Co. in the registry?

The most recently registered devices listed for Douglas C. Mckee & Co. include EYELID SPECULUM.

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