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Matrix Technologies Corp.

United StatesFDA applicant, unverified

Devices
3

What Matrix Technologies Corp. makes

Matrix Technologies Corp. makes the IMPACT and ELECTRAPETTE (R) devices.

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

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

Catalogue3

Newest first, rows 1-3 of 3

  • Impact Ref K940390

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Electrapette (R) Ref K910140

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Impact Ref K961694

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

Frequently asked questions

How many devices does Matrix Technologies Corp. have in the registry?

The registry currently lists 3 devices for Matrix Technologies Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Matrix Technologies Corp.'s devices?

Among its 3 most recently registered devices, Matrix Technologies Corp. has devices listed in FDA 510(k) (3 devices).

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

Among its 3 most recently registered devices, the classes recorded for Matrix Technologies Corp.'s devices are Class I. Each device page shows its own class and authorisation.

What are the newest devices from Matrix Technologies Corp. in the registry?

The most recently registered devices listed for Matrix Technologies Corp. include IMPACT and ELECTRAPETTE (R).

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