Softac Medical Technologies
Country not established
- Devices
- 1
What Softac Medical Technologies makes
Softac Medical Technologies manufactures the EndoFix™ Tissue Fixation System, a device designed for securing soft tissue during surgical procedures, particularly in minimally invasive and endoscopic applications.
The EndoFix™ Tissue Fixation System is classified as a Class II medical device in the US and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
EndoFix™Tissue Fixation System Ref K251229
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Softac Medical Technologies have in the registry?
The registry currently lists 1 device for Softac Medical Technologies. Devices recorded under merged duplicate company entries are counted once.
Which registries list Softac Medical Technologies's devices?
Among its 1 most recently registered device, Softac Medical Technologies has devices listed in FDA 510(k) (1 device).
What risk classes do Softac Medical Technologies's devices fall under?
Among its 1 most recently registered device, the classes recorded for Softac Medical Technologies's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Softac Medical Technologies in the registry?
The most recently registered devices listed for Softac Medical Technologies include EndoFix™Tissue Fixation System.