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Hematology Marketing Assoc.

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Devices
14

What Hematology Marketing Assoc. makes

Hematology Marketing Assoc. makes hematology analyzers, reagents, and calibration products, including devices such as TRI-COUNT 7, LASER-LYSE, LASER-GLOBIN, OSMOCEL +, HEMACAL, OSMOCEL 3, LASER-GLOBIN POWDER, TRI-COUNT CALIBRATOR, LASER-DIL, TRI-COUNT, FOCUS FLUID, and LYSIS +.

These devices are classified as Class I and Class II medical devices and are listed in the FDA 510(k) registry; the company is based in the United States.

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

Catalogue14

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  • Tri-Count 7 Ref K833130

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

  • Laser-Lyse Ref K850097

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

  • Laser-Globin Ref K850096

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

  • Osmocel + Ref K830188

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

  • Hemacal Ref K831306

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

  • Osmocel 3 Ref K851843

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

  • Laser-Globin Powder Ref K850094

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

  • Tri-Count Calibrator Ref K844708

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

  • Laser-Dil Ref K850095

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

  • Tri-Count Ref K851375

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

  • Focus Fluid Ref K830187

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

  • Lysis + Ref K830186

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

  • Tri-Count 10 Ref K834371

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

  • Tri-Count Laser Ref K843485

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

Rows 1-14 of 14

Frequently asked questions

How many devices does Hematology Marketing Assoc. have in the registry?

The registry currently lists 14 devices for Hematology Marketing Assoc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Hematology Marketing Assoc.'s devices?

Among its 14 most recently registered devices, Hematology Marketing Assoc. has devices listed in FDA 510(k) (14 devices).

What risk classes do Hematology Marketing Assoc.'s devices fall under?

Among its 14 most recently registered devices, the classes recorded for Hematology Marketing Assoc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Hematology Marketing Assoc. in the registry?

The most recently registered devices listed for Hematology Marketing Assoc. include TRI-COUNT 7, LASER-LYSE, LASER-GLOBIN and OSMOCEL +.

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