Med-Edge, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Med-Edge, Inc. makes
Med-Edge, Inc. manufactures coronary vein graft markers and coronary vein graft tag markers, which are used to identify and label coronary veins during surgical procedures.
These devices are classified as Class II under FDA regulations and are listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Coronary Vein Graft Marker Ref K882314
Regimes: 510(k) Registry: 510(k)Coronary Vein Graft Tag Marker Ref K971966
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Med-Edge, Inc. have in the registry?
The registry currently lists 2 devices for Med-Edge, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Med-Edge, Inc.'s devices?
Among its 2 most recently registered devices, Med-Edge, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Med-Edge, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Med-Edge, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Med-Edge, Inc. in the registry?
The most recently registered devices listed for Med-Edge, Inc. include CORONARY VEIN GRAFT MARKER and CORONARY VEIN GRAFT TAG MARKER.