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Lode Corp.

United StatesFDA applicant, unverified

Devices
2

What Lode Corp. makes

Lode Corp. manufactures the Corival Ergometer, a device used for assessing and training cardiovascular fitness through cycle ergometry, and the Coagulometer Model LC-6, which measures blood coagulation parameters in laboratory settings.

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

AI-generated from registry data, 3 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Lode Model Corival Ergometer Ref K851097

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Lode Coagulometer Model Lc-6 Ref K852450

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

Frequently asked questions

How many devices does Lode Corp. have in the registry?

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

Which registries list Lode Corp.'s devices?

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

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

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

What are the newest devices from Lode Corp. in the registry?

The most recently registered devices listed for Lode Corp. include LODE MODEL CORIVAL ERGOMETER and LODE COAGULOMETER MODEL LC-6.

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