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Skatron, Inc.

United StatesFDA applicant, unverified

Devices
4

What Skatron, Inc. makes

Skatron, Inc. manufactures laboratory equipment including 96 well dispensers, repeating dispensers, and microplate washing devices. They also produce immunoassay plates for use in laboratory procedures.

The company is based in the United States, and its products are classified as Class I medical devices. These devices are listed within the FDA 510(k) regulatory registry.

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

Catalogue4

Newest first, rows 1-4 of 4

  • 96 Well Dispenser Ref K821961

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Immunoassay Plate Ref K812860

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Skatron Repeating Dispenser Ref K821034

    Active Regimes: 510(k) Registry: 510(k) Class:I
  • Microplate Washing Device Ref K820992

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

Frequently asked questions

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

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

Which registries list Skatron, Inc.'s devices?

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

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

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

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

The most recently registered devices listed for Skatron, Inc. include 96 WELL DISPENSER, IMMUNOASSAY PLATE, SKATRON REPEATING DISPENSER and MICROPLATE WASHING DEVICE.

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