Santerra Medical Technology, Inc.
Country not established
- Devices
- 1
What Santerra Medical Technology, Inc. makes
Santerra Medical Technology, Inc. manufactures 3D anatomical mesh devices designed for surgical applications, providing tailored structural support for tissue reconstruction or repair.
These products are classified as Class II devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
3D Anatomical Mesh Ref K990930
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Santerra Medical Technology, Inc. have in the registry?
The registry currently lists 1 device for Santerra Medical Technology, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Santerra Medical Technology, Inc.'s devices?
Among its 1 most recently registered device, Santerra Medical Technology, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Santerra Medical Technology, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Santerra Medical Technology, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Santerra Medical Technology, Inc. in the registry?
The most recently registered devices listed for Santerra Medical Technology, Inc. include 3D ANATOMICAL MESH.