Episurf Medical, Inc.
Country not established
- Devices
- 1
What Episurf Medical, Inc. makes
Episurf Medical, Inc. manufactures the Episealer Patellofemoral System, a medical device designed for surgical repair of patellofemoral joint injuries, providing fixation solutions for ligamentous reconstructions in the knee.
The company’s portfolio is regulated under FDA’s Class II device classification, with the Episealer Patellofemoral System authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Episealer Patellofemoral System Ref K221048
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Episurf Medical, Inc. have in the registry?
The registry currently lists 1 device for Episurf Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Episurf Medical, Inc.'s devices?
Among its 1 most recently registered device, Episurf Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Episurf Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Episurf Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Episurf Medical, Inc. in the registry?
The most recently registered devices listed for Episurf Medical, Inc. include Episealer Patellofemoral System.