Advanced Uroscience, Inc.
United StatesFDA applicant, unverified
- Devices
- 5
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Advanced Uroscience Innersheath Ref K002573
Regimes: 510(k) Registry: 510(k)Advanced Uroscience Injection Needle Ref K002323
Regimes: 510(k) Registry: 510(k)Advanced Uroscience Injection Needle Ref K982890
Regimes: 510(k) Registry: 510(k)Tissue Marker Ref K001807
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Advanced Uroscience, Inc. have in the registry?
The registry currently lists 5 devices for Advanced Uroscience, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Advanced Uroscience, Inc.'s devices?
Among its 5 most recently registered devices, Advanced Uroscience, Inc. has devices listed in FDA 510(k) (5 devices).
What risk classes do Advanced Uroscience, Inc.'s devices fall under?
Among its 5 most recently registered devices, the classes recorded for Advanced Uroscience, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Advanced Uroscience, Inc. in the registry?
The most recently registered devices listed for Advanced Uroscience, Inc. include ADVANCED UROSCIENCE INNERSHEATH, ADVANCED UROSCIENCE INJECTION NEEDLE, TISSUE MARKER and MODIFICATION TO BRENNEN BIOSYNTHETIC SURGICAL MESH MATRIX.