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Tri-Delta Intl.

Country not established

Devices
1

What Tri-Delta Intl. makes

Tri-Delta Intl. makes medical devices such as the DELTA-FLOW, which is a type of device that falls under the Class II category.

The company's portfolio is regulated and listed in the fda_510k registry, and it is based in the US.

AI-generated from registry data, 30 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

  • Delta-Flow Ref K780479

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

Frequently asked questions

How many devices does Tri-Delta Intl. have in the registry?

The registry currently lists 1 device for Tri-Delta Intl.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Tri-Delta Intl.'s devices?

Among its 1 most recently registered device, Tri-Delta Intl. has devices listed in FDA 510(k) (1 device).

What risk classes do Tri-Delta Intl.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Tri-Delta Intl.'s devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Tri-Delta Intl. in the registry?

The most recently registered devices listed for Tri-Delta Intl. include DELTA-FLOW.

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