Westport Medical, Inc.
Country not established
- Devices
- 1
What Westport Medical, Inc. makes
Westport Medical, Inc. manufactures the PowerTome Periostome, a device designed for periosteal elevation in surgical procedures, aiding in bone exposure and access during orthopedic or dental surgeries.
The PowerTome Periostome is classified as a Class I medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Powertome Periotome Ref K063007
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Westport Medical, Inc. have in the registry?
The registry currently lists 1 device for Westport Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Westport Medical, Inc.'s devices?
Among its 1 most recently registered device, Westport Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Westport Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Westport Medical, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Westport Medical, Inc. in the registry?
The most recently registered devices listed for Westport Medical, Inc. include POWERTOME PERIOTOME.