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Sandare Chemical Co., Inc.

United StatesFDA applicant, unverified

Devices
23

What Sandare Chemical Co., Inc. makes

Sandare Chemical Co., Inc. manufactures laboratory reagents and controls for clinical chemistry testing, including procedures for measuring uric acid, chloride, hemoglobin, total protein, bilirubin, glycated hemoglobin, albumin, phosphorus, and cyanmethemoglobin. Their portfolio also covers specialized tests like the nitroprusside reaction and BCG albumin assays.

The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These reagents and controls are listed in the FDA’s 510(k) database, and the manufacturer is based in the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Sandare Chemical Co., Inc. have in the registry?

The registry currently lists 23 devices for Sandare Chemical Co., Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Sandare Chemical Co., Inc.'s devices?

Among its 23 most recently registered devices, Sandare Chemical Co., Inc. has devices listed in FDA 510(k) (23 devices).

What risk classes do Sandare Chemical Co., Inc.'s devices fall under?

Among its 23 most recently registered devices, the classes recorded for Sandare Chemical Co., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Sandare Chemical Co., Inc. in the registry?

The most recently registered devices listed for Sandare Chemical Co., Inc. include SANDARE URIC ACID PROCEDURE, SANDARE CHLORIDE PROCEDURE, SANDARE HEMOGLOBIN CONTROLS and TOTAL PROTEIN PROCEDURE.

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