Encore Medical, L.P. Dba Djo Surgical
Country not established
- Devices
- 1
What Encore Medical, L.P. Dba Djo Surgical makes
Encore Medical manufactures porous patella implants, designed for use in knee arthroplasty procedures to replace or augment the patellar surface.
The company’s products are classified as Class II devices under FDA regulations and are authorised via the 510(k) pathway. The portfolio is listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Porous Patella Ref K212941
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Encore Medical, L.P. Dba Djo Surgical have in the registry?
The registry currently lists 1 device for Encore Medical, L.P. Dba Djo Surgical. Devices recorded under merged duplicate company entries are counted once.
Which registries list Encore Medical, L.P. Dba Djo Surgical's devices?
Among its 1 most recently registered device, Encore Medical, L.P. Dba Djo Surgical has devices listed in FDA 510(k) (1 device).
What risk classes do Encore Medical, L.P. Dba Djo Surgical's devices fall under?
Among its 1 most recently registered device, the classes recorded for Encore Medical, L.P. Dba Djo Surgical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Encore Medical, L.P. Dba Djo Surgical in the registry?
The most recently registered devices listed for Encore Medical, L.P. Dba Djo Surgical include Porous Patella.