Skip to content

Metrix Teknika, Inc.

United StatesFDA applicant, unverified

Devices
4

What Metrix Teknika, Inc. makes

Metrix Teknika, Inc. manufactures diagnostic and laboratory equipment, including the MINIVISOR for optical analysis, a WASHER SYSTEM for microelisa assays, the FOCISCAN ECHOVISOR SYSTEM for imaging-based diagnostics, and disposable FILTERS for leukocyte removal in blood processing.

The company’s products are regulated under FDA 510(k) clearance, with devices classified as Class I and Class II. They are listed in the FDA’s 510(k) database and are based in the United States.

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

Catalogue4

Newest first, rows 1-4 of 4

  • Minivisor Ref K780035

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Washer System, Microelisa Ref K781802

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Fociscan Echovisor System Ref K781348

    Active Regimes: 510(k) Registry: 510(k) Class:—
  • Filter, Eyrpur Disposable Leukocite Ref K781803

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

Frequently asked questions

How many devices does Metrix Teknika, Inc. have in the registry?

The registry currently lists 4 devices for Metrix Teknika, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Metrix Teknika, Inc.'s devices?

Among its 4 most recently registered devices, Metrix Teknika, Inc. has devices listed in FDA 510(k) (4 devices).

What risk classes do Metrix Teknika, Inc.'s devices fall under?

Among its 4 most recently registered devices, the classes recorded for Metrix Teknika, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Metrix Teknika, Inc. in the registry?

The most recently registered devices listed for Metrix Teknika, Inc. include MINIVISOR, WASHER SYSTEM, MICROELISA, FOCISCAN ECHOVISOR SYSTEM and FILTER, EYRPUR DISPOSABLE LEUKOCITE.

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