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Schiff & Co.

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Devices
15

What Schiff & Co. makes

Schiff & Co. manufactures reusable medical resuscitators, liquid handling dispensers for laboratory use, umbilical catheters, enzyme immunoassay (EIA) test kits, ultraviolet germicidal fixtures and air purification systems, intraosseous perforators for emergency procedures, and enteral feeding tubes. Their portfolio also includes cardiotomy reservoirs for surgical procedures and reactive controls for diagnostic systems.

The company’s devices are regulated under FDA’s Class I and Class II classifications, with most products subject to 510(k) clearance. Their products are listed in the FDA’s 510(k) registry, and the company is based in the United States.

AI-generated from registry data, 1 Oct 2026. Not verified by deviCERTS or the manufacturer.

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Frequently asked questions

How many devices does Schiff & Co. have in the registry?

The registry currently lists 15 devices for Schiff & Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Schiff & Co.'s devices?

Among its 15 most recently registered devices, Schiff & Co. has devices listed in FDA 510(k) (15 devices).

What risk classes do Schiff & Co.'s devices fall under?

Among its 15 most recently registered devices, the classes recorded for Schiff & Co.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from Schiff & Co. in the registry?

The most recently registered devices listed for Schiff & Co. include PLUS REUSABLE RESUSCITATOR, KEMBLE LIQUID HANDLING SYSTEM DISPENSER, VYGON DOUBLE LUMEN UMBILICAL CATHETER and HM-CAP EIA KIT.

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