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Eos Technology Corp.

United StatesFDA applicant, unverified

Devices
2

What Eos Technology Corp. makes

Eos Technology Corp. manufactures the EOS Ionized Calcium Test Card, a diagnostic tool for measuring ionized calcium levels in blood samples, and the EOS Chemistry Analyzer, a device for automated biochemical analysis of clinical specimens.

The company’s products are classified as Class II medical devices under FDA regulations and are listed via the 510(k) clearance process. The manufacturer is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Eos Ionized Calcium Test Card Ref K896316

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Eos Chemistry Analyzer Ref K894035

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

Frequently asked questions

How many devices does Eos Technology Corp. have in the registry?

The registry currently lists 2 devices for Eos Technology Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Eos Technology Corp.'s devices?

Among its 2 most recently registered devices, Eos Technology Corp. has devices listed in FDA 510(k) (2 devices).

What risk classes do Eos Technology Corp.'s devices fall under?

Among its 2 most recently registered devices, the classes recorded for Eos Technology Corp.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Eos Technology Corp. in the registry?

The most recently registered devices listed for Eos Technology Corp. include EOS IONIZED CALCIUM TEST CARD and EOS CHEMISTRY ANALYZER.

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