Oy Ajat, Ltd.
Country not established
- Devices
- 1
What Oy Ajat, Ltd. makes
Oy Ajat, Ltd. manufactures the SCAN300FP, a medical imaging device designed for retroperitoneal scans, and the RETROPAN, a related imaging accessory or system component. These products are intended for diagnostic imaging in abdominal and pelvic regions, providing detailed visualization of anatomical structures.
The company’s portfolio is regulated under Class II medical devices in the United States, with the SCAN300FP and RETROPAN listed via the FDA’s 510(k) clearance process. These devices are authorised for commercial distribution in the US market under applicable regulatory frameworks.
Catalogue
SCAN300FP / Retropan (Vdc) Ref K051664
510(k) 510(k)
Frequently asked questions
How many devices does Oy Ajat, Ltd. have in the registry?
The registry currently lists 1 device for Oy Ajat, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Oy Ajat, Ltd.'s devices?
Among its 1 most recently registered device, Oy Ajat, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Oy Ajat, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Oy Ajat, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Oy Ajat, Ltd. in the registry?
The most recently registered devices listed for Oy Ajat, Ltd. include SCAN300FP / RETROPAN (VDC).