Uros Corp.
Country not established
- Devices
- 1
What Uros Corp. makes
Uros Corp. manufactures the UROSPROBE SYSTEM, Model 1000, a diagnostic device designed for urological imaging and assessment, likely used in evaluating bladder or urethral conditions.
The UROSPROBE SYSTEM, Model 1000 is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Urosprobe System, Model 1000 Ref K960387
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Uros Corp. have in the registry?
The registry currently lists 1 device for Uros Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Uros Corp.'s devices?
Among its 1 most recently registered device, Uros Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Uros Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Uros Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Uros Corp. in the registry?
The most recently registered devices listed for Uros Corp. include UROSPROBE SYSTEM, MODEL 1000.