Medist International
Country not established
- Devices
- 1
What Medist International makes
Medist International manufactures single-size tendon spacers, designed to support soft tissue reconstruction and joint stability in orthopedic procedures.
The company’s products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The manufacturer is based in the United States.
Catalogue
Single Size Tendon Spacer Ref K000019
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Medist International have in the registry?
The registry currently lists 1 device for Medist International. Devices recorded under merged duplicate company entries are counted once.
Which registries list Medist International's devices?
Among its 1 most recently registered device, Medist International has devices listed in FDA 510(k) (1 device).
What risk classes do Medist International's devices fall under?
Among its 1 most recently registered device, the classes recorded for Medist International's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Medist International in the registry?
The most recently registered devices listed for Medist International include SINGLE SIZE TENDON SPACER.