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Redy Laboratories

Country not established

Devices
2

What Redy Laboratories makes

Redy Laboratories manufactures capillary, hollow-fiber dialyzers designed for renal dialysis procedures, including the NEPHROSS 11F100 model.

These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance records. The company is based in the United States.

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

Catalogue2

Newest first, rows 1-2 of 2

  • Dialyzer, Capilatory, Hollow Fiber Ref K772290

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • Nephross 11F100 Ref K790352

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

Frequently asked questions

How many devices does Redy Laboratories have in the registry?

The registry currently lists 2 devices for Redy Laboratories. Devices recorded under merged duplicate company entries are counted once.

Which registries list Redy Laboratories's devices?

Among its 2 most recently registered devices, Redy Laboratories has devices listed in FDA 510(k) (2 devices).

What risk classes do Redy Laboratories's devices fall under?

Among its 2 most recently registered devices, the classes recorded for Redy Laboratories's devices are Class II. Each device page shows its own class and authorisation.

What are the newest devices from Redy Laboratories in the registry?

The most recently registered devices listed for Redy Laboratories include DIALYZER, CAPILATORY, HOLLOW FIBER and NEPHROSS 11F100.

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