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Dialysis Products, Inc.

United StatesFDA applicant, unverified

Devices
2

What Dialysis Products, Inc. makes

Dialysis Products, Inc. manufactures dialysate additives, including the D-LYTE product, which are used in dialysis treatments.

The company's devices are classified as Class II and listed in the FDA 510(k) registry. Dialysis Products, Inc. is based in the US.

AI-generated from registry data, 28 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • Dialysate Additives Ref K842294

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • D-Lyte Ref K833653

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

Frequently asked questions

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

The registry currently lists 2 devices for Dialysis Products, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Dialysis Products, Inc.'s devices?

Among its 2 most recently registered devices, Dialysis Products, Inc. has devices listed in FDA 510(k) (2 devices).

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

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

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

The most recently registered devices listed for Dialysis Products, Inc. include DIALYSATE ADDITIVES and D-LYTE.

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