Unitas Ent.
Country not established
- Devices
- 1
What Unitas Ent. makes
Unitas Ent. manufactures the V.E.P. HIP, a variable endo-prosthesis designed for hip replacement procedures. This device is intended to provide customizable internal fitting within the femoral canal to support stability and alignment during arthroplasty.
The V.E.P. HIP is classified as a Class II medical device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
V.E.P. Hip -Variable Endo-Prosthesis Ref K850928
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Unitas Ent. have in the registry?
The registry currently lists 1 device for Unitas Ent.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Unitas Ent.'s devices?
Among its 1 most recently registered device, Unitas Ent. has devices listed in FDA 510(k) (1 device).
What risk classes do Unitas Ent.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Unitas Ent.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Unitas Ent. in the registry?
The most recently registered devices listed for Unitas Ent. include V.E.P. HIP -VARIABLE ENDO-PROSTHESIS.