Ehicon, Inc.
Country not established
- Devices
- 1
What Ehicon, Inc. makes
Ehicon, Inc. produces ULTRAPRO ADVANCED Macroporous Partially Absorbable Mesh, a medical device used in surgical procedures.
The device is classified as Class II and is listed in the FDA 510(k) registry. Ehicon, Inc. is based in the US.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ehicon, Inc. have in the registry?
The registry currently lists 1 device for Ehicon, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ehicon, Inc.'s devices?
Among its 1 most recently registered device, Ehicon, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Ehicon, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ehicon, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Ehicon, Inc. in the registry?
The most recently registered devices listed for Ehicon, Inc. include ULTRAPRO ADVANCED Macroporous Partically Absorbable Mesh.