Corinth Medtech, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
Catalogue
- Regimes: 510(k) Registry: 510(k)
Veloxion System Ref K230205
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
- Regimes: 510(k) Registry: 510(k)
Veloxion System Ref K162979
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Corinth Medtech, Inc. have in the registry?
The registry currently lists 7 devices for Corinth Medtech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Corinth Medtech, Inc.'s devices?
Among its 7 most recently registered devices, Corinth Medtech, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Corinth Medtech, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Corinth Medtech, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Corinth Medtech, Inc. in the registry?
The most recently registered devices listed for Corinth Medtech, Inc. include Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags, Veloxion System, Veloxion Controller Kit, Veloxion Fluid Control Kit, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch and Veloxion System, Veloxion Controller Kit, Veloxion Resecting Device Kit, Veloxion Fluid Control Set, Veloxion Saline Pole.