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Ekom S.R.O.

Country not established

Devices
2

What Ekom S.R.O. makes

Ekom S.R.O. manufactures medical compressors, including the DK50 D, DK50 DM, and DK50 DS models, designed for delivering compressed air or gases in clinical settings.

These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the US.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Medical Compressor, Models DK50 D And Dm Ref K060781

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • DK50 Ds Ref K091871

    Active Regimes: 510(k) Registry: 510(k) Class:II

Frequently asked questions

How many devices does Ekom S.R.O. have in the registry?

The registry currently lists 2 devices for Ekom S.R.O.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ekom S.R.O.'s devices?

Among its 2 most recently registered devices, Ekom S.R.O. has devices listed in FDA 510(k) (2 devices).

What risk classes do Ekom S.R.O.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Ekom S.R.O.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Ekom S.R.O. in the registry?

The most recently registered devices listed for Ekom S.R.O. include MEDICAL COMPRESSOR, MODELS DK50 D AND DM and DK50 DS.

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