Kubtec
Country not established
Kubtec is a medical device manufacturer, with 30 devices listed in FDA GUDID (FDA Class I and II) as of 15 Nov 2026.
- Devices
- 30
Registry facts
- Registries
- FDA GUDID 30
- Device classes
- FDA Class I 18
- FDA Class II 12
- Identifiers
- DUNS 361955128
What Kubtec makes
Kubtec manufactures portable gamma camera systems, including handheld and mobile units with probes for intraoperative and laparoscopic use, as well as digital x-ray systems for basic diagnostic imaging. Their product line also includes tissue specimen x-ray systems designed for in vitro diagnostics, alongside accessories like carry cases and tablet mounts for imaging devices.
The company’s devices are classified under FDA’s Class I and Class II categories and are listed in the FDA’s Unique Device Identifier (UDI) database. Kubtec operates from the United States.
Catalogue
Search and filter all 30 devicesCompany details
- DUNS number
- 361955128
- apangaio@kubtec.com
- Phone
- 2033648544
Frequently asked questions
How many devices does Kubtec have in the registry?
The registry currently lists 30 devices for Kubtec. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kubtec's devices?
Among its 30 most recently registered devices, Kubtec has devices listed in FDA GUDID (30 devices).
What risk classes do Kubtec's devices fall under?
Among its 30 most recently registered devices, the classes recorded for Kubtec's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Kubtec in the registry?
The most recently registered devices listed for Kubtec include Kubbie Nodes & Shaves Tray A90-0007, Kubbie Container and Nodes & Shaves Tray A90-0001, Kubbie Specimen Membranes and Orientation Markers A90-0002 and Kubbie 3D Specimen Manager K0030C01.