Restore Robotics
Country not established
- Devices
- 1
What Restore Robotics makes
Restore Robotics manufactures robotic surgical instruments, including a permanent cautery hook and a permanent cautery spatula designed for use in minimally invasive procedures.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Restore Robotics have in the registry?
The registry currently lists 1 device for Restore Robotics. Devices recorded under merged duplicate company entries are counted once.
Which registries list Restore Robotics's devices?
Among its 1 most recently registered device, Restore Robotics has devices listed in FDA 510(k) (1 device).
What risk classes do Restore Robotics's devices fall under?
Among its 1 most recently registered device, the classes recorded for Restore Robotics's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Restore Robotics in the registry?
The most recently registered devices listed for Restore Robotics include Robotic Surgical Instruments - Permanent Cautery Hook (470183); Robotic Surgical Instruments - Permanent Cautery Spatula (470184).