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Kontron Instruments, Inc.

Also registered as Kontron Instruments, Ltd.

Country not established

Devices
58

What Kontron Instruments, Inc. makes

Kontron Instruments, Inc. manufactures electronic medical imaging and monitoring devices, including the SIGMA 20 electronic sector scanner and its associated 5MHz transducer, as well as patient monitors like the MINIMON 7137B and KONTRON MINIMON 7134. The company also produces intra-aortic balloon pumps, such as the 10 French percutaneous double lumen and 9.5 French percutaneous double lumen models, along with biopsy kits like the SIGMA 1 WOBBLER. Additional offerings include arrhythmia monitoring modules, temperature monitoring modules, and a patient monitoring system called the KONTRON PMS 7000.

The company’s devices are classified under FDA categories Class I, Class II, and Class III, with submissions recorded in the FDA’s 510(k) registry. These products are listed under U.S. regulatory requirements, 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 Kontron Instruments, Inc. have in the registry?

The registry currently lists 58 devices for Kontron Instruments, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kontron Instruments, Inc.'s devices?

Among its 50 most recently registered devices, Kontron Instruments, Inc. has devices listed in FDA 510(k) (50 devices).

What risk classes do Kontron Instruments, Inc.'s devices fall under?

Among its 50 most recently registered devices, the classes recorded for Kontron Instruments, Inc.'s devices are Class I, Class II and Class III. Each device page shows its own class and authorisation.

What are the newest devices from Kontron Instruments, Inc. in the registry?

The most recently registered devices listed for Kontron Instruments, Inc. include SIGMA 20 ELECTRONIC SECTOR SCANNER, TRANSDUCER FOR KONTROL 5MHZ SIGMA 20, MINIMON 7137B PATIENT MONITOR and 10 FR PERCUTAN DOUBLE LUMEN INTRA-AORTIC BALLOON.

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