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Micro Encapsulation Tech.

Country not established

Devices
3

What Micro Encapsulation Tech. makes

Micro Encapsulation Tech. manufactures single-use, disposable dialysis cartridges—including the DIA-KART, HEMO-KART, and ALU-KART—designed for hemodialysis and related blood purification therapies. These devices are intended for use in extracorporeal blood treatment systems, providing filtration, separation, or exchange functions during medical procedures.

The company’s products are regulated under the FDA’s 510(k) pathway, classifying them as Class II medical devices. These devices are listed in the FDA’s 510(k) database and are intended for commercial distribution in the United States.

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

Catalogue3

Newest first, rows 1-3 of 3

  • Dia-Kart Ref K841180

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

  • Hemo-Kart Ref K841179

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

  • Alu-Kart Ref K841178

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

Frequently asked questions

How many devices does Micro Encapsulation Tech. have in the registry?

The registry currently lists 3 devices for Micro Encapsulation Tech.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Micro Encapsulation Tech.'s devices?

Among its 3 most recently registered devices, Micro Encapsulation Tech. has devices listed in FDA 510(k) (3 devices).

What are the newest devices from Micro Encapsulation Tech. in the registry?

The most recently registered devices listed for Micro Encapsulation Tech. include DIA-KART, HEMO-KART and ALU-KART.

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