Suinsa
Country not established
- Devices
- 1
What Suinsa makes
Suinsa manufactures diagnostic X-ray systems designed for medical imaging, providing radiographic capabilities for clinical diagnostics.
The company’s products are regulated as Class II devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. Suinsa operates from the United States.
Catalogue
Suinsa Diagnostic X-Ray System Ref K083109
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Suinsa have in the registry?
The registry currently lists 1 device for Suinsa. Devices recorded under merged duplicate company entries are counted once.
Which registries list Suinsa's devices?
Among its 1 most recently registered device, Suinsa has devices listed in FDA 510(k) (1 device).
What risk classes do Suinsa's devices fall under?
Among its 1 most recently registered device, the classes recorded for Suinsa's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Suinsa in the registry?
The most recently registered devices listed for Suinsa include SUINSA DIAGNOSTIC X-RAY SYSTEM.