Topez Orthopedics, Inc.
Country not established
- Devices
- 1
What Topez Orthopedics, Inc. makes
Topez Orthopedics, Inc. manufactures the TOPEZ Total Ankle Replacement, a prosthetic device designed for total ankle arthroplasty to restore function and mobility in patients with severe ankle arthritis or degenerative joint disease.
The company’s portfolio is regulated under FDA Class II devices, with the TOPEZ Total Ankle Replacement authorised via the 510(k) pathway. The device is listed in the FDA’s 510(k) database. The company is headquartered in the United States.
Catalogue
Topez Total Ankle Replacement Ref K051023
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Topez Orthopedics, Inc. have in the registry?
The registry currently lists 1 device for Topez Orthopedics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Topez Orthopedics, Inc.'s devices?
Among its 1 most recently registered device, Topez Orthopedics, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Topez Orthopedics, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Topez Orthopedics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Topez Orthopedics, Inc. in the registry?
The most recently registered devices listed for Topez Orthopedics, Inc. include TOPEZ TOTAL ANKLE REPLACEMENT.