Agfa Corp.
Country not established
Agfa Corp. is a medical device manufacturer, with 262 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I) as of 12 Nov 2026.
- Devices
- 262
Registry facts
- Registries
- FDA GUDID 239
- EUDAMED 24
- FDA 510(k) 23
- Device classes
- FDA Class II 206
- FDA Class I 56
What Agfa Corp. makes
Agfa Corp. manufactures manual X-ray film cassettes, digital imaging cassettes, and medical X-ray film with screens for diagnostic imaging. Their portfolio includes storage phosphor screens, indirect flat panel X-ray detectors, and stationary digital X-ray systems, as well as medical printers for film output.
The company’s devices are regulated under FDA classifications, including Class I and Class II, and are listed via 510(k) clearances and the FDA’s Unique Device Identifier (UDI) system.
Catalogue
Search and filter all 262 devicesShowing 1-50 of 262
Frequently asked questions
How many devices does Agfa Corp. have in the registry?
The registry currently lists 262 devices for Agfa Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Agfa Corp.'s devices?
Among its 50 most recently registered devices, Agfa Corp. has devices listed in EUDAMED (6 devices) and FDA GUDID (50 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Agfa Corp.'s devices fall under?
Among its 50 most recently registered devices, the classes recorded for Agfa Corp.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Agfa Corp. in the registry?
The most recently registered devices listed for Agfa Corp. include DX-M 5170/200, CR MD4.0T PLATE 24X30, CURIX ORTHO FAST 24X30 and CR MD4.0T PLATE 15X30.