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Egzotech Sp. Z O. O.

PolandFDA 510(k) applicant, unverified

Devices
1

What Egzotech Sp. Z O. O. makes

Egzotech Sp. Z O. O. manufactures the STELLA BIO, which is a medical device used for rehabilitation and physical therapy.

The company is based in the US, and its device is classified as Class II and listed in the fda_510k registry.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Stella Bio Ref K210002

    Class II
    Active 510(k) 510(k) II

Frequently asked questions

How many devices does Egzotech Sp. Z O. O. have in the registry?

The registry currently lists 1 device for Egzotech Sp. Z O. O.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Egzotech Sp. Z O. O.'s devices?

Among its 1 most recently registered device, Egzotech Sp. Z O. O. has devices listed in FDA 510(k) (1 device).

What risk classes do Egzotech Sp. Z O. O.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Egzotech Sp. Z O. O.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Egzotech Sp. Z O. O. in the registry?

The most recently registered devices listed for Egzotech Sp. Z O. O. include STELLA BIO.

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