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Ppg Industries, Inc.

United StatesFDA applicant, unverified

Devices
20

What Ppg Industries, Inc. makes

The company manufactures patient monitoring and respiratory support devices, including pulse oximeters like the SARA DIGICAP PLUS and OHMEDA MINX, as well as blood gas analyzers such as the STATPAL and STATPAL II systems. Their portfolio also includes ECG and arrhythmia monitoring modules, ventilators (e.g., AV 400 and IRISA models), and flexible transducer catheters for biomedical applications. Additional products cover universal patient monitors (SMU 611) and syringe assemblies for blood gas analysis.

These devices are classified under FDA categories Class I and Class II, with regulatory submissions recorded in the FDA 510(k) database. The manufacturer is based in the United States and its products are listed in the FDA’s 510(k) clearance registry.

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 Ppg Industries, Inc. have in the registry?

The registry currently lists 20 devices for Ppg Industries, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Ppg Industries, Inc.'s devices?

Among its 20 most recently registered devices, Ppg Industries, Inc. has devices listed in FDA 510(k) (20 devices).

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

Among its 20 most recently registered devices, the classes recorded for Ppg Industries, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

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

The most recently registered devices listed for Ppg Industries, Inc. include THE SYSTEM, SARA DIGICAP PLUS OHMEDA MINX OXIMETER, PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER, STATPAL BLOOD GAS MONITORING SYSTEM and CARDIOTEST EK53/EK53R, CARDIOGNOST EK56/EK512.

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