Converg Engineering
Country not established
- Devices
- 1
What Converg Engineering makes
Converg Engineering manufactures the OsteoCNX, a medical device designed for bone regeneration or fixation applications, likely targeting orthopedic procedures.
The OsteoCNX is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
OsteoCNX Ref K223563
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Converg Engineering have in the registry?
The registry currently lists 1 device for Converg Engineering. Devices recorded under merged duplicate company entries are counted once.
Which registries list Converg Engineering's devices?
Among its 1 most recently registered device, Converg Engineering has devices listed in FDA 510(k) (1 device).
What risk classes do Converg Engineering's devices fall under?
Among its 1 most recently registered device, the classes recorded for Converg Engineering's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Converg Engineering in the registry?
The most recently registered devices listed for Converg Engineering include OsteoCNX.