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Kreuzer Corp.

Country not established

Devices
1
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Kreuzer Corp. makes

Kreuzer Corp. manufactures ceiling-mounted support systems, including the Klinoport, designed for patient handling and mobility in clinical environments. These systems are intended to assist healthcare providers in transferring and repositioning patients safely within healthcare settings.

The company’s products fall under FDA Class I medical devices and are listed via the 510(k) pathway. The portfolio is regulated under US FDA standards, and the manufacturer is based in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue1

Newest first, rows 1-1 of 1

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

FDA recall records list 1 recall initiated by Kreuzer Corp., initiated on 2010-10-26. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

  • 2010

    • 26 Oct 2010 Z-0802-2011 Unclassified (pre-2012) Terminated The motorized adjustable pendant arm may suddenly descend to its lowest position. Distribution: Nationwide Distribution -- CT, MA, and MO.

Frequently asked questions

How many devices does Kreuzer Corp. have in the registry?

The registry currently lists 1 device for Kreuzer Corp.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Kreuzer Corp.'s devices?

Among its 1 most recently registered device, Kreuzer Corp. has devices listed in FDA 510(k) (1 device).

What risk classes do Kreuzer Corp.'s devices fall under?

Among its 1 most recently registered device, the classes recorded for Kreuzer Corp.'s devices are Class I. Each device page shows its own class and authorisation.

Are there FDA recall records for Kreuzer Corp.?

FDA recall records list 1 recall initiated by Kreuzer Corp., the most recent initiated on 2010-10-26. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from Kreuzer Corp. in the registry?

The most recently registered devices listed for Kreuzer Corp. include KREUZER CEILING MOUNTED SUPPORT SYSTEMS, KLINOPORT.

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