Soredex Medical Systems
Country not established
- Devices
- 1
What Soredex Medical Systems makes
Soredex Medical Systems manufactures the SPECIMEX DC, a device designed for dental specimen collection and processing, likely used in oral health diagnostics or laboratory analysis.
The SPECIMEX DC is classified as a Class II medical device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Specimex Dc Ref K900740
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Soredex Medical Systems have in the registry?
The registry currently lists 1 device for Soredex Medical Systems. Devices recorded under merged duplicate company entries are counted once.
Which registries list Soredex Medical Systems's devices?
Among its 1 most recently registered device, Soredex Medical Systems has devices listed in FDA 510(k) (1 device).
What risk classes do Soredex Medical Systems's devices fall under?
Among its 1 most recently registered device, the classes recorded for Soredex Medical Systems's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Soredex Medical Systems in the registry?
The most recently registered devices listed for Soredex Medical Systems include SPECIMEX DC.