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S. Cordero Co.

MexicoFDA 510(k) applicant, unverified

Devices
1

What S. Cordero Co. makes

S. Cordero Co. manufactures the S. Cordero Stylus, which is a Class I medical device.

The company is based in the US and its products are listed in the FDA 510(k) registry.

AI-generated from registry data, 27 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • The S. Cordero Stylus Ref K863808

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

Frequently asked questions

How many devices does S. Cordero Co. have in the registry?

The registry currently lists 1 device for S. Cordero Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list S. Cordero Co.'s devices?

Among its 1 most recently registered device, S. Cordero Co. has devices listed in FDA 510(k) (1 device).

What risk classes do S. Cordero Co.'s devices fall under?

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

What are the newest devices from S. Cordero Co. in the registry?

The most recently registered devices listed for S. Cordero Co. include THE S. CORDERO STYLUS.

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